Rhabdomyosarcoma differential diagnosis: Difference between revisions

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__NOTOC__
__NOTOC__
{{Rhabdomyosarcoma}}
[[Image:Home_logo1.png|right|250px|link=https://www.wikidoc.org/index.php/Rhabdomyosarcoma]]
{{CMG}};{{AE}} {{S.M}}
{{CMG}};{{AE}} {{S.M}}


==Overview==
==Overview==
Rhabdomyosarcoma must be differentiated from [[Ewing sarcoma]], [[Lymphadenopathy]], [[Neuroblastoma]], [[Liposarcoma]] [[Osteosarcoma]], Lymphoprofilerative disorders. Rhabdomyosarcoma of the orbit must be differentiated from other causes of orbital masses such as orbital pseudotumor, orbital tumors, orbital abscess, and vascular lesions.
Rhabdomyosarcoma must be differentiated from [[wilms tumor]], [[ewing sarcoma]], [[neuroblastoma]], [[pheochromocytoma]], [[liposarcoma]], [[osteosarcoma]], [[acute myelocytic leukemia]], [[acute lymphoblastic leukemia]], and [[Non-Hodgkin lymphoma|non-hodgkin]] [[lymphoma]]. They mostly differentiated by their [[signs]], [[symptoms]], and [[imaging]] findings. The [[Gold standard (test)|gold standard]] of [[diagnosis]] is usually [[tissue]] [[biopsy]].


==Differential Diagnosis==
==Differential Diagnosis==
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! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Histology
! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Histology
|-
|-
! align="center" style="background:#DCDCDC;" |[[Rhabdomyosarcoma]]<ref name="pmid24966711">{{cite journal| author=Egas-Bejar D, Huh WW| title=Rhabdomyosarcoma in adolescent and young adult patients: current perspectives. | journal=Adolesc Health Med Ther | year= 2014 | volume= 5 | issue=  | pages= 115-25 | pmid=24966711 | doi=10.2147/AHMT.S44582 | pmc=4069040 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24966711  }}</ref><ref name="pmid27955730">{{cite journal| author=Dasgupta R, Fuchs J, Rodeberg D| title=Rhabdomyosarcoma. | journal=Semin Pediatr Surg | year= 2016 | volume= 25 | issue= 5 | pages= 276-283 | pmid=27955730 | doi=10.1053/j.sempedsurg.2016.09.011 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27955730  }}</ref><ref name="pmid18442956">{{cite journal| author=Park K, van Rijn R, McHugh K| title=The role of radiology in paediatric soft tissue sarcomas. | journal=Cancer Imaging | year= 2008 | volume= 8 | issue=  | pages= 102-15 | pmid=18442956 | doi=10.1102/1470-7330.2008.0014 | pmc=2365455 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18442956  }}</ref><ref name="pmid26349418">{{cite journal| author=Shern JF, Yohe ME, Khan J| title=Pediatric Rhabdomyosarcoma. | journal=Crit Rev Oncog | year= 2015 | volume= 20 | issue= 3-4 | pages= 227-43 | pmid=26349418 | doi= | pmc=5486973 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26349418  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Rhabdomyosarcoma]]<ref name="pmid24966711">{{cite journal| author=Egas-Bejar D, Huh WW| title=Rhabdomyosarcoma in adolescent and young adult patients: current perspectives. | journal=Adolesc Health Med Ther | year= 2014 | volume= 5 | issue=  | pages= 115-25 | pmid=24966711 | doi=10.2147/AHMT.S44582 | pmc=4069040 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24966711  }}</ref><ref name="pmid27955730">{{cite journal| author=Dasgupta R, Fuchs J, Rodeberg D| title=Rhabdomyosarcoma. | journal=Semin Pediatr Surg | year= 2016 | volume= 25 | issue= 5 | pages= 276-283 | pmid=27955730 | doi=10.1053/j.sempedsurg.2016.09.011 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27955730  }}</ref><ref name="pmid18442956">{{cite journal| author=Park K, van Rijn R, McHugh K| title=The role of radiology in paediatric soft tissue sarcomas. | journal=Cancer Imaging | year= 2008 | volume= 8 | issue=  | pages= 102-15 | pmid=18442956 | doi=10.1102/1470-7330.2008.0014 | pmc=2365455 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18442956  }}</ref><ref name="pmid26349418">{{cite journal| author=Shern JF, Yohe ME, Khan J| title=Pediatric Rhabdomyosarcoma. | journal=Crit Rev Oncog | year= 2015 | volume= 20 | issue= 3-4 | pages= 227-43 | pmid=26349418 | doi= | pmc=5486973 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26349418  }}</ref>
| align="left" style="background:#F5F5F5;" |
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* Most common [[soft tissue]] [[cancer]] among children and adolescents
* Most common [[soft tissue]] [[cancer]] among children and adolescents
* The third most common extracranial [[solid]] tumors  
* The third most common extracranial [[solid]] tumors  
* Two-third of all cases happen under 6 years old
* Two-third of all cases happen under 6 years old
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| style="background:#F5F5F5;" align="left" | +
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* [[Skin]] changes
* [[Skin]] changes
* [[Respiratory]] difficulties
* [[Respiratory]] difficulties
* Vomitting
* Vomitting
* [[Hematuria]]
* [[Hematuria]]
| align="left" style="background:#F5F5F5;" | +/-
| style="background:#F5F5F5;" align="left" | +/-
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* [[Fever]]
* [[Fever]]
* Erythmatous [[skin]]
* Erythmatous [[skin]]
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* Ophtalmoplasia
* Ophtalmoplasia
* Dysconjugate gaze
* Dysconjugate gaze
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* [[Loss of heterozygosity]] of 11p15.
* [[Loss of heterozygosity]] of 11p15.
[[Mutations]] in:
[[Mutations]] in:
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* FGFR4
* FGFR4
* [[Translocations]] in [[PAX3]] or [[PAX7]] [[genes]] with [[FOXO1]]
* [[Translocations]] in [[PAX3]] or [[PAX7]] [[genes]] with [[FOXO1]]
| align="left" style="background:#F5F5F5;" |[[CT scan]]:
| style="background:#F5F5F5;" align="left" |[[CT scan]]:
* [[Soft tissue]] [[density]]
* [[Soft tissue]] [[density]]
* Enhancement with [[contrast]]
* Enhancement with [[contrast]]
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* [[T1]]:
* [[T1]]:
** Low to intermediate intensity
** Low to intermediate intensity
** [[Hemorrhage]] areas are present in alveolar [[rhabdomyosarcoma]]
** [[Hemorrhage]] areas are present in [[alveolar]] [[rhabdomyosarcoma]]
* [[MRI|T2]]:
* [[MRI|T2]]:
** Hyperintense
** Hyperintense
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|
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|}
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| style="background:#F5F5F5;" align="left" |
* An [[appearance]] of round [[blue]] [[cell]] [[tumors]]  
* An [[appearance]] of round [[blue]] [[cell]] [[tumors]]  
* [[Myogenesis]] pathway has various types of [[differentiation]]
* [[Myogenesis]] pathway has various types of [[differentiation]]
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** [[Myogenin]]
** [[Myogenin]]
|-
|-
! align="center" style="background:#DCDCDC;" |[[Wilms' tumor|Wilms tumor]]<ref name="pmid61529362">{{cite journal |vauthors=Hartman DS, Sanders RC |title=Wilms' tumor versus neuroblastoma: usefulness of ultrasound in differentiation |journal=J Ultrasound Med |volume=1 |issue=3 |pages=117–22 |date=April 1982 |pmid=6152936 |doi= |url=}}</ref><ref name="pmid30036602">{{cite journal |vauthors=De Campo JF |title=Ultrasound of Wilms' tumor |journal=Pediatr Radiol |volume=16 |issue=1 |pages=21–4 |date=1986 |pmid=3003660 |doi= |url=}}</ref><ref name="pmid4080660">{{cite journal |vauthors=Cahan LD |title=Failure of encephalo-duro-arterio-synangiosis procedure in moyamoya disease |journal=Pediatr Neurosci |volume=12 |issue=1 |pages=58–62 |date=1985 |pmid=4080660 |doi= |url=}}</ref><ref name="pmid10985142">{{cite journal| author=Coppes MJ, Pritchard-Jones K| title=Principles of Wilms' tumor biology. | journal=Urol Clin North Am | year= 2000 | volume= 27 | issue= 3 | pages= 423-33, viii | pmid=10985142 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10985142  }}</ref><ref name="pmid22789581">{{cite journal| author=Davidoff AM| title=Wilms tumor. | journal=Adv Pediatr | year= 2012 | volume= 59 | issue= 1 | pages= 247-67 | pmid=22789581 | doi=10.1016/j.yapd.2012.04.001 | pmc=3589819 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22789581  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Wilms' tumor|Wilms tumor]]<ref name="pmid61529362">{{cite journal |vauthors=Hartman DS, Sanders RC |title=Wilms' tumor versus neuroblastoma: usefulness of ultrasound in differentiation |journal=J Ultrasound Med |volume=1 |issue=3 |pages=117–22 |date=April 1982 |pmid=6152936 |doi= |url=}}</ref><ref name="pmid30036602">{{cite journal |vauthors=De Campo JF |title=Ultrasound of Wilms' tumor |journal=Pediatr Radiol |volume=16 |issue=1 |pages=21–4 |date=1986 |pmid=3003660 |doi= |url=}}</ref><ref name="pmid4080660">{{cite journal |vauthors=Cahan LD |title=Failure of encephalo-duro-arterio-synangiosis procedure in moyamoya disease |journal=Pediatr Neurosci |volume=12 |issue=1 |pages=58–62 |date=1985 |pmid=4080660 |doi= |url=}}</ref><ref name="pmid10985142">{{cite journal| author=Coppes MJ, Pritchard-Jones K| title=Principles of Wilms' tumor biology. | journal=Urol Clin North Am | year= 2000 | volume= 27 | issue= 3 | pages= 423-33, viii | pmid=10985142 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10985142  }}</ref><ref name="pmid22789581">{{cite journal| author=Davidoff AM| title=Wilms tumor. | journal=Adv Pediatr | year= 2012 | volume= 59 | issue= 1 | pages= 247-67 | pmid=22789581 | doi=10.1016/j.yapd.2012.04.001 | pmc=3589819 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22789581  }}</ref>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Also called [[nephroblastoma]]
* Also called [[nephroblastoma]]
* The most common childhood [[abdominal]] [[malignancy]]
* The most common childhood [[abdominal]] [[malignancy]]
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|<nowiki>+</nowiki>
|<nowiki>+</nowiki>
| +
| +
| align="left" style="background:#F5F5F5;" |
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* [[Hematuria]]
* [[Hematuria]]
* [[Respiratory]] [[symptoms]] ( due to [[lung]] [[metastases]])
* [[Respiratory]] [[symptoms]] ( due to [[lung]] [[metastases]])
|<nowiki>+/-</nowiki>
|<nowiki>+/-</nowiki>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* [[Fever]]
* [[Fever]]
* [[Hypertension]]/ [[hypotension]]
* [[Hypertension]]/ [[hypotension]]
| align="left" style="background:#F5F5F5;" |Present [[mutations]] of:
| style="background:#F5F5F5;" align="left" |Present [[mutations]] of:
* [[WT1]]
* [[WT1]]
* [[P53]]
* [[P53]]
* FWT1
* FWT1
* FWT2 11p15.5 [[loci]]
* FWT2 11p15.5 [[loci]]
| align="left" style="background:#F5F5F5;" |[[Ultrasound]]:
| style="background:#F5F5F5;" align="left" |[[Ultrasound]]:
*The best initial [[Diagnostic study of choice|diagnostic study]].
*The best initial [[Diagnostic study of choice|diagnostic study]].
*Distinguish [[tumor]] [[mass]] from other causes of renal swelling like [[hydronephrosis]].
*Distinguish [[tumor]] [[mass]] from other causes of renal [[swelling]] like [[hydronephrosis]].
*[[Doppler ultrasonography]] can help to detect [[invasion]] of [[renal vein]] and [[Inferior vena cava|IVC]] by the [[tumor]].
*[[Doppler ultrasonography]] can help to detect [[invasion]] of [[renal vein]] and [[Inferior vena cava|IVC]] by the [[tumor]].
[[CT scan]]:
[[CT scan]]:
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*Surrounding [[organs]] [[invasion]]  
*Surrounding [[organs]] [[invasion]]  
*[[Thrombus]] in [[renal vein]] or [[inferior vena cava]]
*[[Thrombus]] in [[renal vein]] or [[inferior vena cava]]
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
*Arises from mesodermal [[precursors]] of the [[renal]] [[parenchyma]]  
*Arises from mesodermal [[precursors]] of the [[renal]] [[parenchyma]]  
*Well-circumscribed/ macrolobulated [[lesion]]
*Well-circumscribed/ macrolobulated [[lesion]]
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**[[Fibrous connective tissue|Fibrous tissue.]]
**[[Fibrous connective tissue|Fibrous tissue.]]
|-
|-
! align="center" style="background:#DCDCDC;" |[[Ewing sarcoma]]<ref name="pmid12560386">{{cite journal| author=Burchill SA| title=Ewing's sarcoma: diagnostic, prognostic, and therapeutic implications of molecular abnormalities. | journal=J Clin Pathol | year= 2003 | volume= 56 | issue= 2 | pages= 96-102 | pmid=12560386 | doi= | pmc=1769883 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12560386  }}</ref><ref name="pmid8443760">{{cite journal| author=Maygarden SJ, Askin FB, Siegal GP, Gilula LA, Schoppe J, Foulkes M et al.| title=Ewing sarcoma of bone in infants and toddlers. A clinicopathologic report from the Intergroup Ewing's Study. | journal=Cancer | year= 1993 | volume= 71 | issue= 6 | pages= 2109-18 | pmid=8443760 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8443760  }}</ref><ref name="pmid8988217">{{cite journal| author=Panicek DM, Gatsonis C, Rosenthal DI, Seeger LL, Huvos AG, Moore SG et al.| title=CT and MR imaging in the local staging of primary malignant musculoskeletal neoplasms: Report of the Radiology Diagnostic Oncology Group. | journal=Radiology | year= 1997 | volume= 202 | issue= 1 | pages= 237-46 | pmid=8988217 | doi=10.1148/radiology.202.1.8988217 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8988217  }}</ref><ref name="pmid29977059">{{cite journal| author=Grünewald TGP, Cidre-Aranaz F, Surdez D, Tomazou EM, de Álava E, Kovar H et al.| title=Ewing sarcoma. | journal=Nat Rev Dis Primers | year= 2018 | volume= 4 | issue= 1 | pages= 5 | pmid=29977059 | doi=10.1038/s41572-018-0003-x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29977059  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Ewing sarcoma]]<ref name="pmid12560386">{{cite journal| author=Burchill SA| title=Ewing's sarcoma: diagnostic, prognostic, and therapeutic implications of molecular abnormalities. | journal=J Clin Pathol | year= 2003 | volume= 56 | issue= 2 | pages= 96-102 | pmid=12560386 | doi= | pmc=1769883 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12560386  }}</ref><ref name="pmid8443760">{{cite journal| author=Maygarden SJ, Askin FB, Siegal GP, Gilula LA, Schoppe J, Foulkes M et al.| title=Ewing sarcoma of bone in infants and toddlers. A clinicopathologic report from the Intergroup Ewing's Study. | journal=Cancer | year= 1993 | volume= 71 | issue= 6 | pages= 2109-18 | pmid=8443760 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8443760  }}</ref><ref name="pmid8988217">{{cite journal| author=Panicek DM, Gatsonis C, Rosenthal DI, Seeger LL, Huvos AG, Moore SG et al.| title=CT and MR imaging in the local staging of primary malignant musculoskeletal neoplasms: Report of the Radiology Diagnostic Oncology Group. | journal=Radiology | year= 1997 | volume= 202 | issue= 1 | pages= 237-46 | pmid=8988217 | doi=10.1148/radiology.202.1.8988217 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8988217  }}</ref><ref name="pmid29977059">{{cite journal| author=Grünewald TGP, Cidre-Aranaz F, Surdez D, Tomazou EM, de Álava E, Kovar H et al.| title=Ewing sarcoma. | journal=Nat Rev Dis Primers | year= 2018 | volume= 4 | issue= 1 | pages= 5 | pmid=29977059 | doi=10.1038/s41572-018-0003-x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29977059  }}</ref>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Include [[ewing sarcoma]], askin tumor, and peripheral  [[Neuroectodermal tumor primitive|neuroectodermal tumors primitive]]
* Include [[ewing sarcoma]], askin [[tumor]], and peripheral  [[Neuroectodermal tumor primitive|neuroectodermal tumors primitive]]
* The second most common [[childhood]] [[malignant]] primary [[bone]] [[tumors]]  
* The second most common [[childhood]] [[malignant]] primary [[bone]] [[tumors]]  
* Usually arises in the long [[bones]] of the [[extremities]]
* Usually arises in the long [[bones]] of the [[extremities]]
* Common [[age]] between 10-20 years old
* Common [[age]] between 10-20 years old
|<nowiki>+</nowiki>
|<nowiki>+</nowiki>
| align="left" style="background:#F5F5F5;" | +
| style="background:#F5F5F5;" align="left" | +
|
|
* [[Weight loss]]
* [[Weight loss]]
* [[Fatigue]]
* [[Fatigue]]
|<nowiki>+</nowiki>
|<nowiki>+</nowiki>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* [[Fever]]
* [[Fever]]
* [[Pathological|Pathologic]] [[fractures]]
* [[Pathological|Pathologic]] [[fractures]]
* [[Petechiae]]/ [[purpura]]
* [[Petechiae]]/ [[purpura]]
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* [[Reciprocal translocation]] between [[chromosomes]] 11 and 22
* [[Reciprocal translocation]] between [[chromosomes]] 11 and 22
| align="left" style="background:#F5F5F5;" |[[Radiographic]] of region:
| style="background:#F5F5F5;" align="left" |[[Radiographic]] of region:
* Poorly marginated destructive [[lesion]]  
* Poorly marginated destructive [[lesion]]  
* Permeative or "moth-eaten" [[appearance]]
* Permeative or "moth-eaten" [[appearance]]
[[CT scan]]:
[[CT scan]]:
* Cortical destruction  
* [[Cortical area|Cortical]] destruction  
* Demonstrate [[soft tissue]] [[disease]]
* Demonstrate [[soft tissue]] [[disease]]
[[MRI]]:
[[MRI]]:
* Considered as a preferred [[Diagnostic study of choice|diagnostic study]]
* Considered as a preferred [[Diagnostic study of choice|diagnostic study]]
* Better shows [[tumor]] size/ [[intraosseous]]/extraosseous extent
* Better shows [[tumor]] size/ [[intraosseous]]/extraosseous extent
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Small/ round/ [[blue]] cell [[tumors]]
* Small/ round/ [[blue]] cell [[tumors]]
* May be [[undifferentiated]] or differentiated
* May be [[undifferentiated]] or differentiated
* Regular sized [[Primitive (integral)|primitive]] appearing [[Cells (biology)|cells]]
* Regular sized [[Primitive (integral)|primitive]] appearing [[Cells (biology)|cells]]
|-
|-
! align="center" style="background:#DCDCDC;" |Pediatric neuroblastoma <ref name="pmid12110723">{{cite journal| author=Lonergan GJ, Schwab CM, Suarez ES, Carlson CL| title=Neuroblastoma, ganglioneuroblastoma, and ganglioneuroma: radiologic-pathologic correlation. | journal=Radiographics | year= 2002 | volume= 22 | issue= 4 | pages= 911-34 | pmid=12110723 | doi=10.1148/radiographics.22.4.g02jl15911 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12110723  }}</ref><ref name="pmid12580370">{{cite journal| author=Golden CB, Feusner JH| title=Malignant abdominal masses in children: quick guide to evaluation and diagnosis. | journal=Pediatr Clin North Am | year= 2002 | volume= 49 | issue= 6 | pages= 1369-92, viii | pmid=12580370 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12580370  }}</ref><ref name="pmid2403727">{{cite journal| author=Angstman KB, Miser JS, Franz WB| title=Neuroblastoma. | journal=Am Fam Physician | year= 1990 | volume= 41 | issue= 1 | pages= 238-44 | pmid=2403727 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2403727  }}</ref><ref name="pmid6493702">{{cite journal| author=Musarella MA, Chan HS, DeBoer G, Gallie BL| title=Ocular involvement in neuroblastoma: prognostic implications. | journal=Ophthalmology | year= 1984 | volume= 91 | issue= 8 | pages= 936-40 | pmid=6493702 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6493702  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Pediatric]] [[neuroblastoma]] <ref name="pmid12110723">{{cite journal| author=Lonergan GJ, Schwab CM, Suarez ES, Carlson CL| title=Neuroblastoma, ganglioneuroblastoma, and ganglioneuroma: radiologic-pathologic correlation. | journal=Radiographics | year= 2002 | volume= 22 | issue= 4 | pages= 911-34 | pmid=12110723 | doi=10.1148/radiographics.22.4.g02jl15911 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12110723  }}</ref><ref name="pmid12580370">{{cite journal| author=Golden CB, Feusner JH| title=Malignant abdominal masses in children: quick guide to evaluation and diagnosis. | journal=Pediatr Clin North Am | year= 2002 | volume= 49 | issue= 6 | pages= 1369-92, viii | pmid=12580370 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12580370  }}</ref><ref name="pmid2403727">{{cite journal| author=Angstman KB, Miser JS, Franz WB| title=Neuroblastoma. | journal=Am Fam Physician | year= 1990 | volume= 41 | issue= 1 | pages= 238-44 | pmid=2403727 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2403727  }}</ref><ref name="pmid6493702">{{cite journal| author=Musarella MA, Chan HS, DeBoer G, Gallie BL| title=Ocular involvement in neuroblastoma: prognostic implications. | journal=Ophthalmology | year= 1984 | volume= 91 | issue= 8 | pages= 936-40 | pmid=6493702 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6493702  }}</ref>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Most common extracranial solid tumor of infancy
* Most common extracranial [[solid]] [[tumor]] of [[infancy]]
* Arising from  pluripotent sympathetic cells
* Arising from  [[pluripotent]] [[sympathetic]] [[Cells (biology)|cells]]
Age distribution:
[[Age]] distribution:
* < 1 years old ( 40%)  
* < 1 years old ( 40%)  
* 1-2 years old (35%)
* 1-2 years old (35%)
* > 2 years old (25%)
* > 2 years old (25%)
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
+ (Abdominal)
+ ([[Abdominal]])
| align="left" style="background:#F5F5F5;" | +
| style="background:#F5F5F5;" align="left" | +
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* [[Constipation]]
* [[Constipation]]
* [[Weakness]]
* [[Weakness]]
* [[Diarrhea]]
* [[Diarrhea]]
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
+(Abdominal)
+([[Abdominal]])
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* [[Proptosis]]
* [[Proptosis]]
* Periorbital ecchymosis
* Periorbital [[ecchymosis]]
* Horner syndrome
* [[Horner syndrome]]
* Opsoclonus myoclonus syndrome
* [[Opsoclonus myoclonus syndrome]]
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Chromosome1p deletion  
* [[Chromosome]] 1p [[Deletion (genetics)|deletion]]
* N-myc amplification
* [[N-myc-interactor|N-myc]] [[amplification]]
| align="left" style="background:#F5F5F5;" |CT scan:
| style="background:#F5F5F5;" align="left" |[[CT scan]]:
* Heterogeneous mass
* [[Heterogeneous]] [[mass]]
* Calcifications
* [[Calcification]]
* Necrotic areas
* [[Necrotic]] areas
MRI:
[[MRI]]:
*T1:
*[[T1]]:
** heterogeneous mass
** [[heterogeneous]] [[mass]]
*T2:
*[[Magnetic resonance imaging|T2]]:
** heterogeneous/ hyperintense
** [[Heterogeneous]]/ hyperintense
** cystic/necrotic areas  
** [[Cystic]]/ [[necrotic]] areas  
*C+ (Gd):
*C+ (Gd):
** Heterogeneous mass
** [[Heterogeneous]] [[mass]]
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Well defined/ infiltrative mass
* Well defined/ infiltrative [[mass]]
* Homer wright rosettes  
* Homer [[Wright stain|wright]] rosettes  
* Secretion of vanillylmandelic acid (VMA) and homovanillic acid (HVA)
* [[Secretion]] of [[vanillylmandelic acid]] (VMA) and [[homovanillic acid]] (HVA)
|-
|-
! align="center" style="background:#DCDCDC;" |Pediatric pheochromocytoma<ref name="pmid23345359">{{cite journal| author=Leung K, Stamm M, Raja A, Low G| title=Pheochromocytoma: the range of appearances on ultrasound, CT, MRI, and functional imaging. | journal=AJR Am J Roentgenol | year= 2013 | volume= 200 | issue= 2 | pages= 370-8 | pmid=23345359 | doi=10.2214/AJR.12.9126 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23345359  }}</ref><ref name="pmid1988766">{{cite journal| author=Stein PP, Black HR| title=A simplified diagnostic approach to pheochromocytoma. A review of the literature and report of one institution's experience. | journal=Medicine (Baltimore) | year= 1991 | volume= 70 | issue= 1 | pages= 46-66 | pmid=1988766 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1988766  }}</ref><ref name="pmid17876523">{{cite journal| author=Bravo EL| title=Pheochromocytoma: new concepts and future trends. | journal=Kidney Int | year= 1991 | volume= 40 | issue= 3 | pages= 544-56 | pmid=1787652 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1787652  }}</ref><ref name="pmid1787652">{{cite journal| author=Bravo EL| title=Pheochromocytoma: new concepts and future trends. | journal=Kidney Int | year= 1991 | volume= 40 | issue= 3 | pages= 544-56 | pmid=1787652 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1787652  }} </ref>
! style="background:#DCDCDC;" align="center" |[[Pediatric]] [[pheochromocytoma]]<ref name="pmid23345359">{{cite journal| author=Leung K, Stamm M, Raja A, Low G| title=Pheochromocytoma: the range of appearances on ultrasound, CT, MRI, and functional imaging. | journal=AJR Am J Roentgenol | year= 2013 | volume= 200 | issue= 2 | pages= 370-8 | pmid=23345359 | doi=10.2214/AJR.12.9126 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23345359  }}</ref><ref name="pmid1988766">{{cite journal| author=Stein PP, Black HR| title=A simplified diagnostic approach to pheochromocytoma. A review of the literature and report of one institution's experience. | journal=Medicine (Baltimore) | year= 1991 | volume= 70 | issue= 1 | pages= 46-66 | pmid=1988766 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1988766  }}</ref><ref name="pmid17876523">{{cite journal| author=Bravo EL| title=Pheochromocytoma: new concepts and future trends. | journal=Kidney Int | year= 1991 | volume= 40 | issue= 3 | pages= 544-56 | pmid=1787652 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1787652  }}</ref><ref name="pmid1787652">{{cite journal| author=Bravo EL| title=Pheochromocytoma: new concepts and future trends. | journal=Kidney Int | year= 1991 | volume= 40 | issue= 3 | pages= 544-56 | pmid=1787652 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1787652  }} </ref>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Rare catecholamine-secreting tumor
* [[Rare]] [[catecholamine]]-secreting [[tumor]]
* Occur in both children and adults
* Occur in both children and adults
* Average age of 11 years old
* [[Average]] [[age]] of 11 years old
* Associated with  neurofibromatosis, von Hippel-Lindau disease, tuberous sclerosis, Sturge-Weber syndrome, and multiple endocrine neoplasia (MEN) syndromes
* Associated with  [[neurofibromatosis]], [[von Hippel-Lindau disease]], [[tuberous sclerosis]], [[Sturge-Weber syndrome|sturge-weber syndrome]], and [[multiple endocrine neoplasia]] ([[Multiple endocrine neoplasia|MEN]]) [[syndromes]]
| align="left" style="background:#F5F5F5;" |<nowiki>-</nowiki>
| style="background:#F5F5F5;" align="left" |<nowiki>-</nowiki>
| align="left" style="background:#F5F5F5;" |<nowiki>+/-</nowiki>
| style="background:#F5F5F5;" align="left" |<nowiki>+/-</nowiki>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Headache
* [[Headache]]
* sweating
* [[Sweating]]
* Weakness
* [[Weakness]]
* Convulsion
* [[Convulsion]]
| align="left" style="background:#F5F5F5;" |<nowiki>-</nowiki>
| style="background:#F5F5F5;" align="left" |<nowiki>-</nowiki>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Hypertension  
* [[Hypertension]]
* Tachycardia
* [[Tachycardia]]
* Pallor face
* [[Pallor]] [[face]]
|Genetic mutation in:
|[[Genetic]] [[mutation]] in:
* NF1
* [[NF1]]
* RET
* [[RET gene|RET]]
* VHL
* [[VHL]]
* SDHD
* [[SDHD]]
* SDHC
* [[SDHC]]
* EGLN1
* [[EGLN1]]
* EGLN2
* [[EGLN2]]
* KIF1B
* [[KIF1B]]
* SDHAF2
* [[SDHAF2]]
* TMEM127
* [[TMEM127]]
* SDHA
* [[SDHA]]
* IDH1
* [[IDH1]]
* SDHB
* [[SDHB]]
* MAX
* [[MAX (gene)|MAX]]
* HIF2A
* HIF2A
* FH
* [[FH]]
| align="left" style="background:#F5F5F5;" |Ultrasound:
| style="background:#F5F5F5;" align="left" |[[Ultrasound]]:
* Different appearance from solid to mixed cystic or solid to cystic
* Different [[appearance]] from [[solid]] to mixed [[cystic]] or [[solid]] to [[cystic]]
CT scan:
[[CT scan]]:
* Large and heterogenous
* Large and heterogenous
* Calcification
* [[Calcification]]
* Necrosis
* [[Necrosis]]
* Cystic changes
* [[Cystic]] changes
MRI (in extra adrenal tumors):
[[MRI]] (in extra [[adrenal]] [[tumors]]):
*T1:
*[[T1]]:
** Heterogenous enhancement
** Heterogenous enhancement
** Hypointense
** Hypointense
*T2:
*[[MRI|T2]]:
** Hyperintense
** Hyperintense
*T1 C+ (Gd):
*T1 C+ (Gd):
** Heterogenous enhancement
** Heterogenous enhancement
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Zellballen pattern on microscopy  
* Zellballen pattern on [[microscopy]]
* Well-defined clusters
* Well-defined clusters
* Eosinophilic cytoplasm
* [[Eosinophilic]] [[cytoplasm]]
Positive stains for:
Positive stains for:
* Chromogranin for zellballlen cells  
* [[Chromogranin]] for zellballlen [[Cells (biology)|cells]]
* Neurospecific enolase markers for neuronal cells
* Neurospecific [[enolase]] markers for [[neuronal]] [[Cells (biology)|cells]]
* S-100 protein for sustentacular cells  
* [[S-100 protein|S-100]] [[protein]] for [[Sustentacular cell|sustentacular]] [[Cells (biology)|cells]]
|-
|-
! align="center" style="background:#DCDCDC;" |Pediatric osteosarcoma<ref name="pmid8000997">{{cite journal| author=Dorfman HD, Czerniak B| title=Bone cancers. | journal=Cancer | year= 1995 | volume= 75 | issue= 1 Suppl | pages= 203-10 | pmid=8000997 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8000997  }}</ref><ref name="pmid21071381">{{cite journal| author=Yarmish G, Klein MJ, Landa J, Lefkowitz RA, Hwang S| title=Imaging characteristics of primary osteosarcoma: nonconventional subtypes. | journal=Radiographics | year= 2010 | volume= 30 | issue= 6 | pages= 1653-72 | pmid=21071381 | doi=10.1148/rg.306105524 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21071381  }}</ref><ref name="pmid1884549">{{cite journal| author=Araki N, Uchida A, Kimura T, Yoshikawa H, Aoki Y, Ueda T et al.| title=Involvement of the retinoblastoma gene in primary osteosarcomas and other bone and soft-tissue tumors. | journal=Clin Orthop Relat Res | year= 1991 | volume=  | issue= 270 | pages= 271-7 | pmid=1884549 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1884549  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Pediatric]] [[osteosarcoma]]<ref name="pmid8000997">{{cite journal| author=Dorfman HD, Czerniak B| title=Bone cancers. | journal=Cancer | year= 1995 | volume= 75 | issue= 1 Suppl | pages= 203-10 | pmid=8000997 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8000997  }}</ref><ref name="pmid21071381">{{cite journal| author=Yarmish G, Klein MJ, Landa J, Lefkowitz RA, Hwang S| title=Imaging characteristics of primary osteosarcoma: nonconventional subtypes. | journal=Radiographics | year= 2010 | volume= 30 | issue= 6 | pages= 1653-72 | pmid=21071381 | doi=10.1148/rg.306105524 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21071381  }}</ref><ref name="pmid1884549">{{cite journal| author=Araki N, Uchida A, Kimura T, Yoshikawa H, Aoki Y, Ueda T et al.| title=Involvement of the retinoblastoma gene in primary osteosarcomas and other bone and soft-tissue tumors. | journal=Clin Orthop Relat Res | year= 1991 | volume=  | issue= 270 | pages= 271-7 | pmid=1884549 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1884549  }}</ref>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* The second most common primary bone tumor  
* The second most common primary [[bone]] [[tumor]]
* The third most common tumor among adolescents
* The third most common [[tumor]] among adolescents
* Can be primary or secondary
* Can be primary or secondary
* Primary osteosarcoma occurs in age of 10-20 years old
* Primary [[osteosarcoma]] occurs in [[age]] of 10-20 years old
* Secondary osteosarcoma occurs in older patients and is secondary to paget disease and bone infarcts
* Secondary [[osteosarcoma]] occurs in older [[patients]] and is secondary to [[paget disease]] and [[bone]] infarcts
* Accompanied with positive history of trauma
* Accompanied with positive history of [[trauma]]
| align="left" style="background:#F5F5F5;" | +
| style="background:#F5F5F5;" align="left" | +
| align="left" style="background:#F5F5F5;" | +
| style="background:#F5F5F5;" align="left" | +
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Soft tissue swelling
* [[Soft tissue]] [[swelling]]
* Fracture
* [[Fracture]]
* Night sweating
* [[Night Sweats|Night]] [[sweating]]
| align="left" style="background:#F5F5F5;" | +
| style="background:#F5F5F5;" align="left" | +
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Mass swelling
* [[Mass]] [[swelling]]
* Fever
* [[Fever]]
* Arthritis
* [[Arthritis]]
* Decreased joint range of motion
* Decreased [[joint]] [[range of motion]]
* Lymphadenopathy
* [[Lymphadenopathy]]
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Alteration in retinoblastoma gene (Rb)
* Alteration in [[retinoblastoma]] [[gene]] ([[Rb]])
| align="left" style="background:#F5F5F5;" |Plain radiography:
| style="background:#F5F5F5;" align="left" |[[Radiography]]:
* Osteolytic/ osteoblastic feature
* [[Osteolytic metasteses|Osteolytic]]/ [[Osteoblastic osteosarcoma|osteoblastic]] feature
* Periosteum reaction
* [[Periosteum]] reaction
* Calcification or ossification
* [[Calcification]] or [[ossification]]
CT scan:
[[CT scan]]:
* Primary lesion and chest CT are required
* Primary [[lesion]] and [[chest]] [[CT]] are required
* Demonstrate tumor location and extension
* Demonstrate [[tumor]] location and [[extension]]
MRI:
[[MRI]]:
* Exact assessment of tumor extension  
* Exact assessment of [[tumor]] [[extension]]
* Involving joint to joint findings
* Involving [[joint]] to [[joint]] findings
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Contain various cellular pleomorphism and mitoses
* Contain various [[cellular]] [[pleomorphism]] and [[mitoses]]
* Poorly trabecular bone formation
* Poorly [[Trabecular bone|trabecular]] [[bone]] formation
* Fibrocystic and chondroblastic features
* [[Fibrocystic Disease|Fibrocystic]] and chondroblastic features
|-
|-
! align="center" style="background:#DCDCDC;" |Pediatric liposarcoma<ref name="pmid6861094">{{cite journal| author=Shmookler BM, Enzinger FM| title=Liposarcoma occurring in children. An analysis of 17 cases and review of the literature. | journal=Cancer | year= 1983 | volume= 52 | issue= 3 | pages= 567-74 | pmid=6861094 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6861094  }}</ref><ref name="pmid9386667">{{cite journal| author=Marcus KC, Grier HE, Shamberger RC, Gebhardt MC, Perez-Atayde A, Silver B et al.| title=Childhood soft tissue sarcoma: a 20-year experience. | journal=J Pediatr | year= 1997 | volume= 131 | issue= 4 | pages= 603-7 | pmid=9386667 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9386667  }}</ref><ref name="pmid16160117">{{cite journal| author=Murphey MD, Arcara LK, Fanburg-Smith J| title=From the archives of the AFIP: imaging of musculoskeletal liposarcoma with radiologic-pathologic correlation. | journal=Radiographics | year= 2005 | volume= 25 | issue= 5 | pages= 1371-95 | pmid=16160117 | doi=10.1148/rg.255055106 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16160117  }}</ref><ref name="pmid17372913">{{cite journal| author=Italiano A, Cardot N, Dupré F, Monticelli I, Keslair F, Piche M et al.| title=Gains and complex rearrangements of the 12q13-15 chromosomal region in ordinary lipomas: the "missing link" between lipomas and liposarcomas? | journal=Int J Cancer | year= 2007 | volume= 121 | issue= 2 | pages= 308-15 | pmid=17372913 | doi=10.1002/ijc.22685 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17372913  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Pediatric]] [[liposarcoma]]<ref name="pmid6861094">{{cite journal| author=Shmookler BM, Enzinger FM| title=Liposarcoma occurring in children. An analysis of 17 cases and review of the literature. | journal=Cancer | year= 1983 | volume= 52 | issue= 3 | pages= 567-74 | pmid=6861094 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6861094  }}</ref><ref name="pmid9386667">{{cite journal| author=Marcus KC, Grier HE, Shamberger RC, Gebhardt MC, Perez-Atayde A, Silver B et al.| title=Childhood soft tissue sarcoma: a 20-year experience. | journal=J Pediatr | year= 1997 | volume= 131 | issue= 4 | pages= 603-7 | pmid=9386667 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9386667  }}</ref><ref name="pmid16160117">{{cite journal| author=Murphey MD, Arcara LK, Fanburg-Smith J| title=From the archives of the AFIP: imaging of musculoskeletal liposarcoma with radiologic-pathologic correlation. | journal=Radiographics | year= 2005 | volume= 25 | issue= 5 | pages= 1371-95 | pmid=16160117 | doi=10.1148/rg.255055106 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16160117  }}</ref><ref name="pmid17372913">{{cite journal| author=Italiano A, Cardot N, Dupré F, Monticelli I, Keslair F, Piche M et al.| title=Gains and complex rearrangements of the 12q13-15 chromosomal region in ordinary lipomas: the "missing link" between lipomas and liposarcomas? | journal=Int J Cancer | year= 2007 | volume= 121 | issue= 2 | pages= 308-15 | pmid=17372913 | doi=10.1002/ijc.22685 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17372913  }}</ref>
|Considered as a nonrhabdomyosarcoma soft tissue sarcomas
|
One of the least frequent tumors during  childhood
* Considered as a nonrhabdomyosarcoma [[soft tissue]] [[sarcomas]]
 
* One of the least frequent [[tumors]] during  [[childhood]]
Rarely seen in adolescents and age of < 8 years old
* Rarely seen in adolescents and [[age]] of < 8 years old
 
* [[Average]] [[age]] is 50 years among adults
Average age is 50 years among adults
* Occur mostly in [[lower extremities]][[retroperitoneal]] region, and [[shoulder]]
 
| style="background:#F5F5F5;" align="left" | +
Occur mostly in lower extremities,  retroperitoneal region, and shoulder  
| style="background:#F5F5F5;" align="left" | +/-
| align="left" style="background:#F5F5F5;" | +
| style="background:#F5F5F5;" align="left" |
| align="left" style="background:#F5F5F5;" | +/-
* [[Weight loss]]
| align="left" style="background:#F5F5F5;" |
* [[Fatigue]]
* Weight loss
| style="background:#F5F5F5;" align="left" | -
* Fatigue
| style="background:#F5F5F5;" align="left" |
| align="left" style="background:#F5F5F5;" | -
| align="left" style="background:#F5F5F5;" |
* N/A
* N/A
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Amplification of 12q13–15 region in  MDM2 and CDK4 genes
* [[Amplification]] of 12q13–15 region in  [[MDM2]] and [[CDK4]] [[genes]]
* Translocation of  t(12;16)(q13;p11.2) in myxoid liposarcoma
* [[Translocations|Translocation]] of  t (12;16) (q13;p11.2) in myxoid [[liposarcoma]]
| align="left" style="background:#F5F5F5;" |CT scan:
| style="background:#F5F5F5;" align="left" |[[CT scan]]:
* Inhomogenous fatty structure
* Inhomogenous fatty structure
* Tumor mineralization
* [[Tumor]] [[mineralization]]
* Cortical bone erosion
* [[Cortical bone|Cortical]] [[bone]] erosion
* Calcification
* [[Calcification]]
* Infiltration to medistinum
* Infiltration to [[mediastinum]]
MRI:
[[MRI]]:
* Adipose content mass
* [[Adipose]] content [[mass]]
* Thin irregular [[septa]]
* Thin [[Irregular bone|irregular]] [[septa]]
* Hemorrhage
* [[Hemorrhage]]
* Necrosis areas
* [[Necrosis]] areas
| align="left" style="background:#F5F5F5;" |Divided into following subtypes:
| style="background:#F5F5F5;" align="left" |Divided into following subtypes:
* Well-differentiated
* Well-differentiated
* Dedifferentiated, Myxoid/roundcell
* Dedifferentiated, Myxoid/ round [[cell]]
* Pleomorphic
* [[Pleomorphic]]
Common findings:
Common findings:
* Lipoblasts presence
* Lipoblasts presence
* Cytoplasmic lipid vacuoles
* [[Cytoplasmic]] [[lipid]] [[vacuoles]]
* Chromatin spikes
* [[Chromatin]] spikes
|-
|-
! align="center" style="background:#DCDCDC;" |Pediatric acute myelocystic leukemia<ref name="pmid18064533">{{cite journal| author=Yamamoto JF, Goodman MT| title=Patterns of leukemia incidence in the United States by subtype and demographic characteristics, 1997-2002. | journal=Cancer Causes Control | year= 2008 | volume= 19 | issue= 4 | pages= 379-90 | pmid=18064533 | doi=10.1007/s10552-007-9097-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18064533  }}</ref><ref name="pmid23634996">{{cite journal| author=Cancer Genome Atlas Research Network. Ley TJ, Miller C, Ding L, Raphael BJ, Mungall AJ et al.| title=Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. | journal=N Engl J Med | year= 2013 | volume= 368 | issue= 22 | pages= 2059-74 | pmid=23634996 | doi=10.1056/NEJMoa1301689 | pmc=3767041 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23634996  }}</ref><ref name="pmid3864727">{{cite journal| author=Islam A, Catovsky D, Goldman JM, Galton DA| title=Bone marrow biopsy changes in acute myeloid leukaemia. I: Observations before chemotherapy. | journal=Histopathology | year= 1985 | volume= 9 | issue= 9 | pages= 939-57 | pmid=3864727 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3864727  }}</ref><ref name="pmid17587881">{{cite journal| author=Orazi A| title=Histopathology in the diagnosis and classification of acute myeloid leukemia, myelodysplastic syndromes, and myelodysplastic/myeloproliferative diseases. | journal=Pathobiology | year= 2007 | volume= 74 | issue= 2 | pages= 97-114 | pmid=17587881 | doi=10.1159/000101709 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17587881  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Pediatric]] [[acute myelocytic leukemia]]<ref name="pmid18064533">{{cite journal| author=Yamamoto JF, Goodman MT| title=Patterns of leukemia incidence in the United States by subtype and demographic characteristics, 1997-2002. | journal=Cancer Causes Control | year= 2008 | volume= 19 | issue= 4 | pages= 379-90 | pmid=18064533 | doi=10.1007/s10552-007-9097-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18064533  }}</ref><ref name="pmid23634996">{{cite journal| author=Cancer Genome Atlas Research Network. Ley TJ, Miller C, Ding L, Raphael BJ, Mungall AJ et al.| title=Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. | journal=N Engl J Med | year= 2013 | volume= 368 | issue= 22 | pages= 2059-74 | pmid=23634996 | doi=10.1056/NEJMoa1301689 | pmc=3767041 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23634996  }}</ref><ref name="pmid3864727">{{cite journal| author=Islam A, Catovsky D, Goldman JM, Galton DA| title=Bone marrow biopsy changes in acute myeloid leukaemia. I: Observations before chemotherapy. | journal=Histopathology | year= 1985 | volume= 9 | issue= 9 | pages= 939-57 | pmid=3864727 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3864727  }}</ref><ref name="pmid17587881">{{cite journal| author=Orazi A| title=Histopathology in the diagnosis and classification of acute myeloid leukemia, myelodysplastic syndromes, and myelodysplastic/myeloproliferative diseases. | journal=Pathobiology | year= 2007 | volume= 74 | issue= 2 | pages= 97-114 | pmid=17587881 | doi=10.1159/000101709 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17587881  }}</ref>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Replacement of normal bone marrow cells with abnormal cells
* Replacement of [[normal]] [[Bone marrow cells|bone marrow]] [[Cells (biology)|cells]] with [[abnormal]] [[Cells (biology)|cells]]
* Myeloblast is malignant cell
* [[Myeloblasts|Myeloblast]] is [[malignant]] [[cell]]
* Wide distribution among childhood to adults
* Wide [[Distribution (pharmacology)|distribution]] among [[childhood]] to adults
* Survival rate of 60%
* [[Survival rate]] of 60%
* Common in down syndrome
* Common in [[down syndrome]]
| align="left" style="background:#F5F5F5;" |<nowiki>+/- ( Abdominal mass, mediastinal mass)</nowiki>
| style="background:#F5F5F5;" align="left" | +/- ( [[Abdominal]] [[mass]], [[mediastinal]] [[mass]])
| align="left" style="background:#F5F5F5;" |<nowiki>+ (bone pain, joint pain)</nowiki>
| style="background:#F5F5F5;" align="left" | + ([[bone]] [[pain]], [[joint]] [[pain]])
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Bleeding  
* [[Bleeding]]
* Infectious
* [[Infectious]]
|<nowiki>+/-</nowiki>
|<nowiki>+/-</nowiki>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Lymphadenopathy
* [[Lymphadenopathy]]
* Hepatosplenomegaly
* [[Hepatosplenomegaly]]
* Bruising
* [[Bruising]]
* Petechiae
* [[Petechiae]]
* Pallor face
* [[Pallor]] [[face]]
* Anemia
* [[Anemia]]
* Fever
* [[Fever]]
| align="left" style="background:#F5F5F5;" |Genetic translocations include:
| style="background:#F5F5F5;" align="left" |[[Genetic]] [[translocations]] include:
*t(8;21)
*t (8;21)
*t(3;21)
*t (3;21)
*t(15;17)
*t (15;17)
| align="left" style="background:#F5F5F5;" |Radiography:
| style="background:#F5F5F5;" align="left" |[[Radiography]]:
*Chest radiography:
*[[Chest]] [[radiography]]:
** Diagnosis of mediastinal mass
** [[Diagnosis]] of [[mediastinal]] [[mass]]
*Extremities radiography:
*[[Extremities]] [[radiography]]:
** Metaphyseal bands   
** [[Metaphyseal]] [[bands]]  
** Lytic lesions
** [[Lytic]] [[lesions]]
** New periosteal bone formation  
** New [[Periosteal reaction|periosteal]] [[bone]] formation  
** Pathologic fractures
** [[Pathological|Pathologic]] [[fractures]]
CT scan/ MRI:
[[CT scan]]/ [[MRI]]:
* Thickening/ edema of the bowel wall in presence of abdominal pain or bowl infection
* Thickening/ [[edema]] of the [[bowel]] wall in presence of [[abdominal]] [[pain]] or [[bowel]] [[infection]]
* Detection of early sinusitis
* Detection of early [[sinusitis]]
* Intracranial hemorrhage in presence of neurological symptoms
* [[Intracranial hemorrhage|Intracranial]] [[hemorrhage]] in presence of [[neurological]] [[symptoms]]
Radionuclide imaging:
[[Radionuclide test|Radionuclide]] [[imaging]]:
* Detection of occult infection
* [[Detection theory|Detection]] of [[occult]] [[infection]]
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Hyperplastic bone marrow with leukemia cells replacement
* [[Hyperplastic]] [[bone marrow]] with [[leukemia]] [[Cells (biology)|cells]] replacement
* Megaloblastic feature
* [[Megaloblastic Anemias|Megaloblastic]] feature
* decrease in normal hematopoietic cell
* Decrease in [[normal]] [[hematopoietic cell]]
|-
|-
! align="center" style="background:#DCDCDC;" |Pediatric acute lymphoblastic leukemia<ref name="pmid25184049">{{cite journal| author=Zuckerman T, Rowe JM| title=Pathogenesis and prognostication in acute lymphoblastic leukemia. | journal=F1000Prime Rep | year= 2014 | volume= 6 | issue=  | pages= 59 | pmid=25184049 | doi=10.12703/P6-59 | pmc=4108947 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25184049  }}</ref><ref name="pmid18358930">{{cite journal| author=Pui CH, Robison LL, Look AT| title=Acute lymphoblastic leukaemia. | journal=Lancet | year= 2008 | volume= 371 | issue= 9617 | pages= 1030-43 | pmid=18358930 | doi=10.1016/S0140-6736(08)60457-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18358930  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Pediatric]] [[acute lymphoblastic leukemia]]<ref name="pmid25184049">{{cite journal| author=Zuckerman T, Rowe JM| title=Pathogenesis and prognostication in acute lymphoblastic leukemia. | journal=F1000Prime Rep | year= 2014 | volume= 6 | issue=  | pages= 59 | pmid=25184049 | doi=10.12703/P6-59 | pmc=4108947 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25184049  }}</ref><ref name="pmid18358930">{{cite journal| author=Pui CH, Robison LL, Look AT| title=Acute lymphoblastic leukaemia. | journal=Lancet | year= 2008 | volume= 371 | issue= 9617 | pages= 1030-43 | pmid=18358930 | doi=10.1016/S0140-6736(08)60457-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18358930  }}</ref>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* The most common malignancy among children
* The most common [[malignancy]] among children
* Few cases may associated with down syndrome, wiskott-aldrich syndrome, andataxia-telangiectasia
* Few cases may associated with [[down syndrome]], wiskott-   aldrich syndrome, and [[ataxia-telangiectasia]]
* Peak age of 2-5 years old
* Peak [[age]] of 2-5 years old
* Previous history of cancer/ drug exposure
* Previous history of [[cancer]]/ [[drug]] [[Exposure (photography)|exposure]]
* Bone marrow replaced with malognant lymphoblasts
* [[Bone marrow]] replaced with [[malignant]] [[lymphoblasts]]
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
+/-( Extramedullary masses in  abdomen/ head/neck)
+/-( Extramedullary [[mass]] in  [[abdomen]]/ [[head]]/ [[neck]])
| align="left" style="background:#F5F5F5;" | +/- (Musculoskeletal pain)
| style="background:#F5F5F5;" align="left" | +/- ([[Musculoskeletal]] [[pain]])
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Weakness
* [[Weakness]]
* Fatigue
* [[Fatigue]]
* Weight loss
* [[Weight loss]]
* Bleesing
* [[Bleeding]]
| align="left" style="background:#F5F5F5;" | -
| style="background:#F5F5F5;" align="left" | -
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Fever
* [[Fever]]
* Lymphadenopathy
* [[Lymphadenopathy]]
* Hepatosplenomegaly
* [[Hepatosplenomegaly]]
* [[Pallor]]
* [[Pallor]]
* [[Papilledema]]
* [[Papilledema]]
Line 406: Line 404:
* [[Cranial nerve palsy]]
* [[Cranial nerve palsy]]
* [[Dyspnea]]
* [[Dyspnea]]
| align="left" style="background:#F5F5F5;" |Chromosomal translocations:
| style="background:#F5F5F5;" align="left" |[[Chromosomal]] [[translocations]]:
* t(9;22)  
* t (9;22)  
* t(12;21)
* t (12;21)
* t(5;14)
* t (5;14)
* t(1;19)
* t (1;19)
| align="left" style="background:#F5F5F5;" |Radiography:
| style="background:#F5F5F5;" align="left" |[[Radiography]]:
Chest x ray:
[[Chest]] [[x ray]]:
* Nodular masses
* [[Nodular]] [[mass]]
* Central lymphadenopathy
* [[Central]] [[lymphadenopathy]]
Bone x ray:
[[Bone]] [[x ray]]:
* Radiolucent metaphyseal bands
* Radiolucent [[metaphyseal]] [[bands]]
* Coarse trabeculation
* Coarse trabeculation
* Periosteal reactions
* [[Periosteal reaction]]
* Osteopenia
* [[Osteopenia]]
Brain MRI:
[[Brain]] [[MRI]]:
* Leukoencephalopathy
* [[Leukoencephalopathy]]
* Glial cell hyperplasia
* [[Glial cell]] [[hyperplasia]]
* Meningitis
* [[Meningitis]]
| align="left" style="background:#F5F5F5;" |Divided into 3 subgroups:
| style="background:#F5F5F5;" align="left" |Divided into 3 subgroups:
L1:
L1:
* Small lymphoblast cells
* Small [[lymphoblast]] [[Cells (biology)|cells]]
* Scant cytoplasm
* Scant [[cytoplasm]]
* Invisible nucleoli
* Invisible [[nucleoli]]
L2:
L2:
* Larger lymphoblast cells
* Larger [[lymphoblast]] [[Cells (biology)|cells]]
* Abundant cytoplasm
* Abundant [[cytoplasm]]
* Prominent nucleoli
* Prominent [[nucleoli]]
L3:
L3:
* Large lymphoblast cells
* Large [[lymphoblast]] [[Cells (biology)|cells]]
* Deep cytoplasmic basophilia
* Deep [[cytoplasmic]] [[basophilia]]
* Similar to Burkitt lymphoma  
* Similar to [[Burkitt lymphoma]]
|-
|-
! align="center" style="background:#DCDCDC;" |Pediatric non-hodgkin lymphoma<ref name="pmid23297126">{{cite journal| author=Green MR, Gentles AJ, Nair RV, Irish JM, Kihira S, Liu CL et al.| title=Hierarchy in somatic mutations arising during genomic evolution and progression of follicular lymphoma. | journal=Blood | year= 2013 | volume= 121 | issue= 9 | pages= 1604-11 | pmid=23297126 | doi=10.1182/blood-2012-09-457283 | pmc=3587323 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23297126  }}</ref><ref name="pmid26174528">{{cite journal| author=Sandlund JT| title=Non-Hodgkin Lymphoma in Children. | journal=Curr Hematol Malig Rep | year= 2015 | volume= 10 | issue= 3 | pages= 237-43 | pmid=26174528 | doi=10.1007/s11899-015-0277-y | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26174528  }}</ref><ref name="pmid25655608">{{cite journal| author=El-Galaly TC, Hutchings M| title=Imaging of non-Hodgkin lymphomas: diagnosis and response-adapted strategies. | journal=Cancer Treat Res | year= 2015 | volume= 165 | issue=  | pages= 125-46 | pmid=25655608 | doi=10.1007/978-3-319-13150-4_5 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25655608  }}</ref>
! style="background:#DCDCDC;" align="center" |[[Pediatric]] [[Non-Hodgkin lymphoma|non-hodgkin]] [[lymphoma]]<ref name="pmid23297126">{{cite journal| author=Green MR, Gentles AJ, Nair RV, Irish JM, Kihira S, Liu CL et al.| title=Hierarchy in somatic mutations arising during genomic evolution and progression of follicular lymphoma. | journal=Blood | year= 2013 | volume= 121 | issue= 9 | pages= 1604-11 | pmid=23297126 | doi=10.1182/blood-2012-09-457283 | pmc=3587323 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23297126  }}</ref><ref name="pmid26174528">{{cite journal| author=Sandlund JT| title=Non-Hodgkin Lymphoma in Children. | journal=Curr Hematol Malig Rep | year= 2015 | volume= 10 | issue= 3 | pages= 237-43 | pmid=26174528 | doi=10.1007/s11899-015-0277-y | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26174528  }}</ref><ref name="pmid25655608">{{cite journal| author=El-Galaly TC, Hutchings M| title=Imaging of non-Hodgkin lymphomas: diagnosis and response-adapted strategies. | journal=Cancer Treat Res | year= 2015 | volume= 165 | issue=  | pages= 125-46 | pmid=25655608 | doi=10.1007/978-3-319-13150-4_5 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25655608  }}</ref>
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Cancer derives from lymphocytes
* [[Cancer]] derives from [[lymphocytes]]
* diverse age of incidence
* Diverse [[age]] of incidence
* Associated with autoimmune disorders, previous cancer therapy, and infection
* Associated with [[autoimmune disorders]], previous [[cancer]] [[therapy]], and [[infection]]
| align="left" style="background:#F5F5F5;" | +
| style="background:#F5F5F5;" align="left" | +
| align="left" style="background:#F5F5F5;" | -
| style="background:#F5F5F5;" align="left" | -
| align="left" style="background:#F5F5F5;" |
| style="background:#F5F5F5;" align="left" |
* Lymph node swelling
* [[Lymph node]] [[swelling]]
* Weight loss
* [[Weight loss]]
* Anorexia
* [[Anorexia]]
* Abdominal pain
* [[Abdominal]] [[pain]]


* Nausea/ vomitting
* [[Nausea]]/ [[vomiting]]
| align="left" style="background:#F5F5F5;" | + ([[Chest]] [[tenderness]])
| style="background:#F5F5F5;" align="left" | + ([[Chest]] [[tenderness]])
| align="left" style="background:#F5F5F5;" |Fever
| style="background:#F5F5F5;" align="left" |
Hepatosplenomegaly
* [[Fever]]
Lymphadenopathy
* [[Hepatosplenomegaly]]
Seizure
* [[Lymphadenopathy]]
Petechiae
* [[Seizure]]
| align="left" style="background:#F5F5F5;" |
* [[Petechiae]]
| style="background:#F5F5F5;" align="left" |
* [[MLL2]]
* [[MLL2]]
* [[MEF2B]]
* [[MEF2B]]
Line 465: Line 464:
* [[KMT2D]]
* [[KMT2D]]
* [[CDKN2A]]
* [[CDKN2A]]
| align="left" style="background:#F5F5F5;" |Radiography:
| style="background:#F5F5F5;" align="left" |[[Radiography]]:
*Chest x ray:
*[[Chest]] [[x ray]]:
** Central lymphadenopathy
** [[Central]] [[lymphadenopathy]]
** Pleural effusion
** [[Pleural effusion]]
** Pericardial effusion
** [[Pericardial effusion]]
CT scan:
[[CT scan]]:
* Presence of enlarged lymph node in chest, abdomen, and pelvis
* Presence of enlarged [[lymph node]] in [[chest]], [[abdomen]], and [[pelvis]]
Ultrasound:
[[Ultrasound]]:
* Hepatosplenomegaly
* [[Hepatosplenomegaly]]
| align="left" style="background:#F5F5F5;" |Histology findings of non-hodgkin lymphoma depend on:
| style="background:#F5F5F5;" align="left" |[[Histology]] findings of [[Non-Hodgkin lymphoma|non-hodgkin]] [[lymphoma]] depend on:
* Cell differentiation
* [[Cell]] [[differentiation]]
* Cell lineage
* [[Cell]] [[Lineage (evolution)|lineage]]
* Location of cell origin
* Location of [[cell]] [[origin]]
|}
|}



Latest revision as of 13:26, 2 April 2019

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Shadan Mehraban, M.D.[2]

Overview

Rhabdomyosarcoma must be differentiated from wilms tumor, ewing sarcoma, neuroblastoma, pheochromocytoma, liposarcoma, osteosarcoma, acute myelocytic leukemia, acute lymphoblastic leukemia, and non-hodgkin lymphoma. They mostly differentiated by their signs, symptoms, and imaging findings. The gold standard of diagnosis is usually tissue biopsy.

Differential Diagnosis

Disease History/demography Symptoms Physical examination Diagnosis
Palpable mass Pain Others Mass tenderness Others Genetics Imaging Histology
Rhabdomyosarcoma[1][2][3][4]
  • Most common soft tissue cancer among children and adolescents
  • The third most common extracranial solid tumors
  • Two-third of all cases happen under 6 years old
+ + +/-

Mutations in:

CT scan:

Ultrasound:

MRI:

Wilms tumor[5][6][7][8][9] + + +/- Present mutations of: Ultrasound:

CT scan:

Ewing sarcoma[10][11][12][13] + + + Radiographic of region:

CT scan:

MRI:

Pediatric neuroblastoma [14][15][16][17]

Age distribution:

  • < 1 years old ( 40%)
  • 1-2 years old (35%)
  • > 2 years old (25%)

+ (Abdominal)

+

+(Abdominal)

CT scan:

MRI:

Pediatric pheochromocytoma[18][19][20][21] - +/- - Genetic mutation in: Ultrasound:

CT scan:

MRI (in extra adrenal tumors):

  • T1:
    • Heterogenous enhancement
    • Hypointense
  • T2:
    • Hyperintense
  • T1 C+ (Gd):
    • Heterogenous enhancement

Positive stains for:

Pediatric osteosarcoma[22][23][24] + + + Radiography:

CT scan:

MRI:

Pediatric liposarcoma[25][26][27][28] + +/- -
  • N/A
CT scan:

MRI:

Divided into following subtypes:

Common findings:

Pediatric acute myelocytic leukemia[29][30][31][32] +/- ( Abdominal mass, mediastinal mass) + (bone pain, joint pain) +/- Genetic translocations include:
  • t (8;21)
  • t (3;21)
  • t (15;17)
Radiography:

CT scan/ MRI:

Radionuclide imaging:

Pediatric acute lymphoblastic leukemia[33][34]

+/-( Extramedullary mass in abdomen/ head/ neck)

+/- (Musculoskeletal pain) - Chromosomal translocations:
  • t (9;22)
  • t (12;21)
  • t (5;14)
  • t (1;19)
Radiography:

Chest x ray:

Bone x ray:

Brain MRI:

Divided into 3 subgroups:

L1:

L2:

L3:

Pediatric non-hodgkin lymphoma[35][36][37] + - + (Chest tenderness) Radiography:

CT scan:

Ultrasound:

Histology findings of non-hodgkin lymphoma depend on:

References

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