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==Overview==
==Overview==
[[Merkel cell carcinoma]] ([[MCC]]) is an unusual [[cutaneous]] [[malignancy]] of [[neuroendocrine]] origin.Merkel [[Nerve ending|nerve endings]] are [[mechanoreceptors]] in the skin.[[Merkel cells]] are normal components in the basal layer of the [[Epidermis (skin)|epidermis]] of the skin.
Merkel cell carcinoma ([[MCC]]) is an unusual [[cutaneous]] [[malignancy]] of [[neuroendocrine]] origin.Merkel [[Nerve ending|nerve endings]] are [[mechanoreceptors]] in the skin.[[Merkel cells]] are normal components in the basal layer of the [[Epidermis (skin)|epidermis]] of the skin.


==Pathophysiology==
==Pathophysiology==
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* Merkel cell polyomavirus belongs to [[DNA virus]] which has no [[Envelope (biology)|envelop]] and it is double stranded.
* Merkel cell polyomavirus belongs to [[DNA virus]] which has no [[Envelope (biology)|envelop]] and it is double stranded.
* According to new research, specific [[Deletion (genetics)|deletion]] in the VP1 gene on MCPyV([[merkel cell]] [[polyomavirus]]) may lead to [[merkel cell carcinoma]].<ref name="pmid18593898">{{cite journal |vauthors=Kassem A, Schöpflin A, Diaz C, Weyers W, Stickeler E, Werner M, Zur Hausen A |title=Frequent detection of Merkel cell polyomavirus in human Merkel cell carcinomas and identification of a unique deletion in the VP1 gene |journal=Cancer Res. |volume=68 |issue=13 |pages=5009–13 |date=July 2008 |pmid=18593898 |doi=10.1158/0008-5472.CAN-08-0949 |url=}}</ref>
* According to new research, specific [[Deletion (genetics)|deletion]] in the VP1 gene on MCPyV([[merkel cell]] [[polyomavirus]]) may lead to [[merkel cell carcinoma]].<ref name="pmid18593898">{{cite journal |vauthors=Kassem A, Schöpflin A, Diaz C, Weyers W, Stickeler E, Werner M, Zur Hausen A |title=Frequent detection of Merkel cell polyomavirus in human Merkel cell carcinomas and identification of a unique deletion in the VP1 gene |journal=Cancer Res. |volume=68 |issue=13 |pages=5009–13 |date=July 2008 |pmid=18593898 |doi=10.1158/0008-5472.CAN-08-0949 |url=}}</ref>
* Large T [[antigen]] were found to be associated with MCPyV and development of [[merkel cell carcinoma]].
* [[Antigen|Large T antigen]] were found to be associated with MCPyV and development of [[merkel cell carcinoma]].
* It is thought that MCPyV([[merkel cell]] [[polyomavirus]]) is a normal [[flora]] of the skin and sheds chronically.<ref name="pmid20542254">{{cite journal |vauthors=Schowalter RM, Pastrana DV, Pumphrey KA, Moyer AL, Buck CB |title=Merkel cell polyomavirus and two previously unknown polyomaviruses are chronically shed from human skin |journal=Cell Host Microbe |volume=7 |issue=6 |pages=509–15 |date=June 2010 |pmid=20542254 |pmc=2919322 |doi=10.1016/j.chom.2010.05.006 |url=}}</ref>
* It is thought that MCPyV([[merkel cell]] [[polyomavirus]]) is a normal [[flora]] of the skin and sheds chronically.<ref name="pmid20542254">{{cite journal |vauthors=Schowalter RM, Pastrana DV, Pumphrey KA, Moyer AL, Buck CB |title=Merkel cell polyomavirus and two previously unknown polyomaviruses are chronically shed from human skin |journal=Cell Host Microbe |volume=7 |issue=6 |pages=509–15 |date=June 2010 |pmid=20542254 |pmc=2919322 |doi=10.1016/j.chom.2010.05.006 |url=}}</ref>
* Two major oncoproteins were encoded by MCPyV([[merkel cell]] [[polyomavirus]]):
* Two major oncoproteins were encoded by MCPyV([[merkel cell]] [[polyomavirus]]):
** Large tumor (LT) [[antigen]] and
** Large tumor (LT) [[antigen]]
** Small tumor (sT) [[antigen]]
** Small tumor (ST) [[antigen]]
* Both large tumor (LT) [[antigen]] and small tumor (sT) [[antigen]] believed to be play a crucial role in the development of [[merkel cell carcinoma]].
* Both large tumor (LT) [[antigen]] and small tumor (ST) [[antigen]] believed to be play a crucial role in the development of [[merkel cell carcinoma]].
* MCPyV([[merkel cell]] [[polyomavirus]]) [[pathogenesis]] in sequential order:
* MCPyV([[merkel cell]] [[polyomavirus]]) [[pathogenesis]] in sequential order:
*# Integration of viral [[genome]] into the host [[genome]]
*# Integration of viral [[genome]] into the host [[genome]].
*# Increased expression of small tumor (sT) antigen after integration
*# Increased expression of small tumor (ST) antigen after integration.
*# Gaining of [[mutations]] in the 3' end of large tumor (LT) antigen which results in the production of truncated molecule  
*# Gaining of [[mutations]] in the 3 end of large tumor (LT) antigen which results in the production of truncated molecule.
*# And finally evade the [[immune response]] by the body  
*# And finally evade the [[immune response]] by the body.


'''UV radiation'''
'''UV radiation'''
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* The risk of developing [[merkel cell carcinoma]] increases in fair skin individuals.<ref name="pmid14576661">{{cite journal |vauthors=Agelli M, Clegg LX |title=Epidemiology of primary Merkel cell carcinoma in the United States |journal=J. Am. Acad. Dermatol. |volume=49 |issue=5 |pages=832–41 |date=November 2003 |pmid=14576661 |doi=10.1067/S0190 |url=}}</ref>
* The risk of developing [[merkel cell carcinoma]] increases in fair skin individuals.<ref name="pmid14576661">{{cite journal |vauthors=Agelli M, Clegg LX |title=Epidemiology of primary Merkel cell carcinoma in the United States |journal=J. Am. Acad. Dermatol. |volume=49 |issue=5 |pages=832–41 |date=November 2003 |pmid=14576661 |doi=10.1067/S0190 |url=}}</ref>
* [[Incidence]] is directly proportional to [[sun exposure]] in developing [[merkel cell carcinoma]].<ref name="pmid21711338">{{cite journal |vauthors=Girschik J, Thorn K, Beer TW, Heenan PJ, Fritschi L |title=Merkel cell carcinoma in Western Australia: a population-based study of incidence and survival |journal=Br. J. Dermatol. |volume=165 |issue=5 |pages=1051–7 |date=November 2011 |pmid=21711338 |doi=10.1111/j.1365-2133.2011.10493.x |url=}}</ref>
* [[Incidence]] is directly proportional to [[sun exposure]] in developing [[merkel cell carcinoma]].<ref name="pmid21711338">{{cite journal |vauthors=Girschik J, Thorn K, Beer TW, Heenan PJ, Fritschi L |title=Merkel cell carcinoma in Western Australia: a population-based study of incidence and survival |journal=Br. J. Dermatol. |volume=165 |issue=5 |pages=1051–7 |date=November 2011 |pmid=21711338 |doi=10.1111/j.1365-2133.2011.10493.x |url=}}</ref>
* Patients who are undergoing [[PUVA]] therapy have an increased risk of developing [[merkel cell carcinoma]].
* Patients who are undergoing [[PUVA]] therapy have an inceased risk of developing [[merkel cell carcinoma]].
* The exact [[pathogenesis]] of how [[ultraviolet]] ([[Ultraviolet|UV]]) [[radiation]] exposure leads to [[merkel cell carcinoma]] is not completely understood.
* The exact [[pathogenesis]] of how [[ultraviolet]] ([[Ultraviolet|UV]]) [[radiation]] exposure leads to [[merkel cell carcinoma]] is not completely understood.
'''Immunosuppression'''  
'''Immunosuppression'''  
* Patients who underwent [[organ transplant]] are also very also prone to developing [[merkel cell carcinoma]] due to [[immunosuppression]].
* Patients who underwent [[organ transplant]] are also very prone to developing [[merkel cell carcinoma]] due to [[immunosuppression]].
* Patients who are suffering with [[Human Immunodeficiency Virus (HIV)|HIV]] and [[malignancies]] especially [[B cell]] origin are also likely prone to develop [[merkel cell carcinoma]] due to [[immunosuppression]].
* Patients who are suffering with [[Human Immunodeficiency Virus (HIV)|HIV]] and [[malignancies]] especially [[B cell]] origin are also likely prone to develop [[merkel cell carcinoma]] due to [[immunosuppression]].
* The exact [[pathogenesis]] of how [[immunosuppression]] leads to [[merkel cell carcinoma]] is not completely understood.
* The exact [[pathogenesis]] of how [[immunosuppression]] leads to [[merkel cell carcinoma]] is not completely understood.
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* PIK3CA
* PIK3CA
* KNSTRN
* KNSTRN
* [[PREX2]], and
* [[PREX2]]
* [[RAC1]]
* [[RAC1]]
==Gross Pathology==
==Gross Pathology==

Latest revision as of 02:19, 31 January 2019

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Overview

Merkel cell carcinoma (MCC) is an unusual cutaneous malignancy of neuroendocrine origin.Merkel nerve endings are mechanoreceptors in the skin.Merkel cells are normal components in the basal layer of the epidermis of the skin.

Pathophysiology

Physiology

The normal physiology of merkel cells can be understood as follows:[1]

Pathogenesis

Merkel cell polyomavirus

UV radiation

Immunosuppression

Genetics

Genes involved in the pathogenesis of merkel cell carcinoma include:

Gross Pathology

On gross pathology of merkel cell carcinoma

Merkel cell carcinoma gross pathology
Merkel cell carcinoma gross pathologyhttps://commons.wikimedia.org/wiki/File:Merkel_Cell_Carcinoma_buttock_45-year-old_woman.jpg#/media/File:Merkel_Cell_Carcinoma_buttock_45-year-old_woman.jpg

Microscopic Pathology

On microscopic histopathological analysis, trabecular pattern, monotonous round tumor cells, mitotic figures, atypical fibroxanthoma-like areas and dusty chromatin are characteristic findings of merkel cell carcinoma.

Merkel cell carcinoma
Merkel cell carcinomahttps://commons.wikimedia.org/wiki/File:Merkel_cell_carcinoma_-_very_high_mag.jpg#/media/File:Merkel_cell_carcinoma_-_very_high_mag.jpg

References

  1. Halata, Zdenek; Grim, Milos; Bauman, Klaus I. (2003). "Friedrich Sigmund Merkel and his ?Merkel cell?, morphology, development, and physiology: Review and new results". The Anatomical Record. 271A (1): 225–239. doi:10.1002/ar.a.10029. ISSN 0003-276X.
  2. Feng H, Shuda M, Chang Y, Moore PS (February 2008). "Clonal integration of a polyomavirus in human Merkel cell carcinoma". Science. 319 (5866): 1096–100. doi:10.1126/science.1152586. PMC 2740911. PMID 18202256.
  3. Sharp CP, Norja P, Anthony I, Bell JE, Simmonds P (February 2009). "Reactivation and mutation of newly discovered WU, KI, and Merkel cell carcinoma polyomaviruses in immunosuppressed individuals". J. Infect. Dis. 199 (3): 398–404. doi:10.1086/596062. PMID 19090778.
  4. Carter JJ, Paulson KG, Wipf GC, Miranda D, Madeleine MM, Johnson LG, Lemos BD, Lee S, Warcola AH, Iyer JG, Nghiem P, Galloway DA (November 2009). "Association of Merkel cell polyomavirus-specific antibodies with Merkel cell carcinoma". J. Natl. Cancer Inst. 101 (21): 1510–22. doi:10.1093/jnci/djp332. PMC 2773184. PMID 19776382.
  5. Kassem A, Schöpflin A, Diaz C, Weyers W, Stickeler E, Werner M, Zur Hausen A (July 2008). "Frequent detection of Merkel cell polyomavirus in human Merkel cell carcinomas and identification of a unique deletion in the VP1 gene". Cancer Res. 68 (13): 5009–13. doi:10.1158/0008-5472.CAN-08-0949. PMID 18593898.
  6. Schowalter RM, Pastrana DV, Pumphrey KA, Moyer AL, Buck CB (June 2010). "Merkel cell polyomavirus and two previously unknown polyomaviruses are chronically shed from human skin". Cell Host Microbe. 7 (6): 509–15. doi:10.1016/j.chom.2010.05.006. PMC 2919322. PMID 20542254.
  7. Heath M, Jaimes N, Lemos B, Mostaghimi A, Wang LC, Peñas PF, Nghiem P (March 2008). "Clinical characteristics of Merkel cell carcinoma at diagnosis in 195 patients: the AEIOU features". J. Am. Acad. Dermatol. 58 (3): 375–81. doi:10.1016/j.jaad.2007.11.020. PMC 2335370. PMID 18280333.
  8. Miller RW, Rabkin CS (February 1999). "Merkel cell carcinoma and melanoma: etiological similarities and differences". Cancer Epidemiol. Biomarkers Prev. 8 (2): 153–8. PMID 10067813.
  9. Agelli M, Clegg LX (November 2003). "Epidemiology of primary Merkel cell carcinoma in the United States". J. Am. Acad. Dermatol. 49 (5): 832–41. doi:10.1067/S0190. PMID 14576661.
  10. Girschik J, Thorn K, Beer TW, Heenan PJ, Fritschi L (November 2011). "Merkel cell carcinoma in Western Australia: a population-based study of incidence and survival". Br. J. Dermatol. 165 (5): 1051–7. doi:10.1111/j.1365-2133.2011.10493.x. PMID 21711338.