Dermatofibroma differential diagnosis: Difference between revisions

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! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Histopathology
! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Histopathology
|-
|-
! colspan="2" |Dermatofibroma
| colspan="2" style="background: #C0C0C0; padding: 5px; text-align: center;" |'''Dermatofibroma'''
!Nodule
| style="background: #F5F5F5; padding: 5px;" |
!Hyperpigmented
* Nodule
!Firm
| style="background: #F5F5F5; padding: 5px;" |
!0.3- 1 cm
*Hyperpigmented
!Mostly seen in extremities
| style="background: #F5F5F5; padding: 5px;" |
!
*Firm
!
| style="background: #F5F5F5; padding: 5px;" |
*0.3- 1 cm
| style="background: #F5F5F5; padding: 5px;" |
*Mostly seen in extremities
| style="background: #F5F5F5; padding: 5px;" |
* Localized [[nodular]] [[proliferation]] of [[spindle]]-shaped [[fibrous]] [[Cells (biology)|cells]] in a [[mixture]] of [[Histiocyte|histocytoid]] [[Cells (biology)|cells]] inside the [[dermis]]
* Localized [[nodular]] [[proliferation]] of [[spindle]]-shaped [[fibrous]] [[Cells (biology)|cells]] in a [[mixture]] of [[Histiocyte|histocytoid]] [[Cells (biology)|cells]] inside the [[dermis]]
* Spiculated margin of cells
* Spiculated margin of cells
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* "Grenz zone"  
* "Grenz zone"  
* [[Epidermal]] [[hyperplasia]]
* [[Epidermal]] [[hyperplasia]]
| style="background: #F5F5F5; padding: 5px;" |
!
!
|-
|-
! colspan="2" |Dermatofibrosarcoma Protuberum<br />
| colspan="2" style="background: #C0C0C0; padding: 5px; text-align: center;" |'''Dermatofibrosarcoma Protuberum'''<br />
!
!
!
!
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!
|-
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! colspan="2" |[[Kaposi sarcoma]]
| colspan="2" style="background: #C0C0C0; padding: 5px; text-align: center;" |'''[[Kaposi sarcoma]]'''
!
!
!
!

Revision as of 21:42, 22 August 2019

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

Overview

Deep penetrating dermatofibroma may be difficult to distinguish, even histologically, from rare malignant fibrohistocytic tumors e.g dermatofibrosarcoma protuberans.

Differential Diagnosis

Immunohistochemical Staining

Neoplasm CD34 Stromelysin-3 Factor XIIIa
Dermatofibroma + + +
Dermatofibrosarcoma protuberans + - -

Overview

[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].

OR

[Disease name] must be differentiated from [[differential dx1], [differential dx2], and [differential dx3].

Differentiating [Disease name] from other Diseases

[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].

OR

[Disease name] must be differentiated from [differential dx1], [differential dx2], and [differential dx3].

OR

As [disease name] manifests in a variety of clinical forms, differentiation must be established in accordance with the particular subtype. [Subtype name 1] must be differentiated from other diseases that cause [clinical feature 1], such as [differential dx1] and [differential dx2]. In contrast, [subtype name 2] must be differentiated from other diseases that cause [clinical feature 2], such as [differential dx3] and [differential dx4].

Differentiating [disease name] from other diseases on the basis of [symptom 1], [symptom 2], and [symptom 3]

On the basis [symptom 1], [symptom 2], and [symptom 3], [disease name] must be differentiated from [disease 1], [disease 2], [disease 3], [disease 4], [disease 5], and [disease 6].

Diseases Skin examination Diagnosis Additional findings
Type Color Texture Size Distribution Dermoscopic Findings Histopathology
Dermatofibroma
  • Nodule
  • Hyperpigmented
  • Firm
  • 0.3- 1 cm
  • Mostly seen in extremities
Dermatofibrosarcoma Protuberum
Kaposi sarcoma
Cutaneous squamous cell carcinoma[3] SCC in situ (Bowen's disease)
  • Scaly
  • Variable
  • Fair-skinned individuals: sun-exposed areas
  • Presence of dotted and/or glomerular vessels
  • White to yellowish surface scales
  • Red-yellowish background
  • Slow growth over the years
Invasive squamous cell carcinoma
  • Skin colored
  • 0.5 to 1.5 cm
  • Fair-skinned individuals: sun-exposed areas
  • In black individuals: legs, anus, and areas of chronic inflammation
  • White circles
  • White structureless areas
  • Masses of keratin
  • Hairpin and linear-irregular vessels
Keratoacanthoma[4]
  • Macule
  • Papule
  • May have telangiectasias
  • Skin-colored
  • Mildly erythematous
  • Prominent keratinous core in the center of the nodule
  • 1 to 2.5 cm
  • Sun-exposed areas
  • Face, neck, hands, and arms
  • White circles
  • Keratin
  • Blood spots
  • White structureless zones
  • Dermal inflammatory infiltrate
  • Rapid growth (within weeks)
Merkel cell carcinoma[5]
  • Shiny
  • Flesh-colored or bluish-red
  • Firm
  • < 1 cm
  • Sun-exposed areas
  • Milky red areas
  • Linear
  • Irregular vessels
  • Polymorphous vessels
  • Older individuals with light skin tones
  • Rapidly growing
Basal cell carcinoma[6] Nodular basal cell carcinoma
  • Flesh-colored
  • Small bump
  • Variable
  • Focused, bright red, and branching arborizing vessels
  • Loosely arranged blue-gray dots
  • Nest-like infiltration with basaloid cells
  • May have a "rolled" border
Superficial basal cell carcinoma
  • Patch
  • Scaly
  • 1 to > 10 cm
  • Sun-exposed areas
  • Head (cheek and nose)
  • Trunk
  • Superficial fine telangiectasia
  • Shiny white to red, translucent or opaque structureless areas
  • Multiple small erosions
  • Large, hyperchromatic, oval nuclei
  • Minimal cytoplasm
  • Small basaloid nodules
Sclerosing basal cell carcinoma (morpheaform)[7]
  • Papule
  • Plaque
  • Variable
  • Sun-exposed areas
Prurigo nodules[8][9]
  • Firm
  • Few millimeters to several centimeters
  • Extensor surfaces of the arms and legs and on the trunk
  • Upper back, abdomen, and sacrum
  • White "starburst pattern" surrounding red/brown/yellow crusts
  • Erosions
  • Hyperkeratosis
  • Thick and compact orthohyperkeratosis
  • Irregular epidermal hyperplasia
  • Focal parakeratosis with irregular acanthosis
  • Nonspecific dermal infiltrate containing WBCs
  • Nodules range in number from few to hundreds
  • Worsened by heat, sweating, or irritation from clothing
Melanoma[10] Melanoma in situ (Lentigo Maligna)[11]
  • Variable (from light to dark brown, black, pink, red, or white)
  • Smooth
  • Around 1 cm
  • Sun-damaged skin of the head or neck
  • Asymmetric, pigmented follicular openings
  • Gray angulated lines
  • Gray areas, dots, and globules
  • Circle within a circle
  • Darkening of pigmentation, sharpening of borders, or emergence of nodular areas are signs of progression to lentigo maligna melanoma
Lentigo maligna melanoma[12]
  • Brown/tan
  • Freckle-like
  • Variable
  • Chronically sun-damaged areas
  • Asymmetric, pigmented follicular openings
  • Gray angulated lines
  • Gray areas, dots, and globules
  • Circle within a circle
  • Usually in older individuals
Superficial spreading melanoma[13]
  • Macule
  • Plaque with irregular borders
  • Variably pigmented (red, blue, black, gray, and white)
  • Thin
  • 1 mm to > 1 cm
  • Anywhere but usually:
    • Back (men and women)
    • Lower extremities (women)
  • Asymmetry of shape
  • > 2 colors
  • Asymmetry of structures
  • Asymmetric
  • Poorly circumscribed
  • Lack cellular maturation
  • Lateral (radial) growth before vertical (invasive) growth
Nodular melanoma[14][15]
  • Dark color
  • Lump
  • 6mm to > 1 cm
  • Trunk
  • Head
  • Neck
  • Pigment network or pseudonetwork
  • Aggregated brown or black globules
  • Blue pigmentation within lesion
  • Small dotted or comma vessels
  • Dermal growth in isolation or in association with an epidermal component
  • Two-thirds arise in normal skin, the rest in existing moles
  • Rapidly enlarging
Acral lentiginous melanoma[16]
  • Dark brown to black
  • Variable
  • Palmar
  • Plantar
  • Subungual
  • Mucosal surfaces
  • Parallel-ridge pattern
  • Irregular diffuse pigmentation
  • Asymmetric proliferation of single melanocytes at dermoepidermal junction
  • Most common among dark skinned individuals
Amelanotic melanoma[17]
  • Patch
  • Skin color
  • Slightly elevated borders
  • Around 6 mm
  • Sun-exposed areas
  • Dotted vessels
  • Linear irregular vessels
Common nevus[18][19]
  • Smooth surface
  • Terminal hairs often present
  • 1 cm to > 20 cm
  • Sun-exposed areas above the waist
  • Comma-shaped or curved vessels
  • Structureless light brown background
  • Residual brown thick circles around the hair follicles
  • Also called Miescher nevus
Blue nevus[20]
  • Blue
  • Smooth
  • Variable
  • Head and neck,
  • Dorsal aspect of the distal extremities
  • Sacral area
  • Structureless blue pigmentation
  • Structureless blue and white or blue and brown on some occasions
  • Proliferation of dendritic, dermal, melanin-producing melanocytes
  • Also called Mongolian spots
Spitz nevus[21][22] Nonpigmented Spitz nevus
  • Pink
  • Smooth
  • < 1 cm
  • Cheek
  • Coiled vessels
  • White network over a pink to reddish background
  • In children and adolescents
Reed-like Spitz[23]
  • Papule
  • Smooth
  • < 1 cm
  • Head and neck
  • Upper and lower extremities
  • Enlarged spindle melanocytes with polyangular form
  • "Ground glass" cytoplasm
  • Most commonly develops in children, adolescents, and young adults.
Solar lentigo[24]
  • Multiple spots
  • Brown
  • Smooth
  • Around 5mm
  • Sun-exposed areas
  • Faint pigmented fingerprint structures
  • Structureless pattern
  • Light brown pseudonetwork with well-defined borders and a "moth-eaten" edge
  • Associated with UV exposure and skin aging
Sebaceous hyperplasia[25]
  • Skin-colored to brownish
  • Umbilicated
  • 2 - 6 mm
  • Structureless yellow to whitish center surrounded by short linear "crown vessels"
  • Usually in middle-aged or older patients
Lichen planus-like keratosis[26]
  • Gray to brown
  • Prominent
  • Variable
  • Appearance depends on stage of evolution

References

  1. Hanly AJ, Jordà M, Elgart GW, Badiavas E, Nassiri M, Nadji M (2006). "High proliferative activity excludes dermatofibroma: report of the utility of MIB-1 in the differential diagnosis of selected fibrohistiocytic tumors". Arch. Pathol. Lab. Med. 130 (6): 831–4. doi:10.1043/1543-2165(2006)130[831:HPAEDR]2.0.CO;2. PMID 16740036. Unknown parameter |month= ignored (help)
  2. Kim HJ, Lee JY, Kim SH; et al. (2007). "Stromelysin-3 expression in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans: comparison with factor XIIIa and CD34". Br. J. Dermatol. 157 (2): 319–24. doi:10.1111/j.1365-2133.2007.08033.x. PMID 17596171. Unknown parameter |month= ignored (help)
  3. Petter G, Haustein UF (2000). "Histologic subtyping and malignancy assessment of cutaneous squamous cell carcinoma". Dermatol Surg. 26 (6): 521–30. PMID 10848931.
  4. Kwiek B, Schwartz RA (2016). "Keratoacanthoma (KA): An update and review". J Am Acad Dermatol. 74 (6): 1220–33. doi:10.1016/j.jaad.2015.11.033. PMID 26853179.
  5. Albores-Saavedra J, Batich K, Chable-Montero F, Sagy N, Schwartz AM, Henson DE (2010). "Merkel cell carcinoma demographics, morphology, and survival based on 3870 cases: a population based study". J Cutan Pathol. 37 (1): 20–7. doi:10.1111/j.1600-0560.2009.01370.x. PMID 19638070.
  6. Wolberink EA, Pasch MC, Zeiler M, van Erp PE, Gerritsen MJ (2013). "High discordance between punch biopsy and excision in establishing basal cell carcinoma subtype: analysis of 500 cases". J Eur Acad Dermatol Venereol. 27 (8): 985–9. doi:10.1111/j.1468-3083.2012.04628.x. PMID 22759209.
  7. Wrone DA, Swetter SM, Egbert BM, Smoller BR, Khavari PA (1996). "Increased proportion of aggressive-growth basal cell carcinoma in the Veterans Affairs population of Palo Alto, California". J Am Acad Dermatol. 35 (6): 907–10. PMID 8959949.
  8. Errichetti E, Piccirillo A, Stinco G (2015). "Dermoscopy of prurigo nodularis". J Dermatol. 42 (6): 632–4. doi:10.1111/1346-8138.12844. PMID 25808786.
  9. Weigelt N, Metze D, Ständer S (2010). "Prurigo nodularis: systematic analysis of 58 histological criteria in 136 patients". J Cutan Pathol. 37 (5): 578–86. doi:10.1111/j.1600-0560.2009.01484.x. PMID 20002240.
  10. Witt C, Krengel S (2010). "Clinical and epidemiological aspects of subtypes of melanocytic nevi (Flat nevi, Miescher nevi, Unna nevi)". Dermatol Online J. 16 (1): 1. PMID 20137743.
  11. Connolly KL, Giordano C, Dusza S, Busam KJ, Nehal K (2019). "Follicular involvement is frequent in lentigo maligna: Implications for treatment". J Am Acad Dermatol. 80 (2): 532–537. doi:10.1016/j.jaad.2018.07.071. PMC 6333487. PMID 30266559.
  12. Connolly KL, Giordano C, Dusza S, Busam KJ, Nehal K (2019). "Follicular involvement is frequent in lentigo maligna: Implications for treatment". J Am Acad Dermatol. 80 (2): 532–537. doi:10.1016/j.jaad.2018.07.071. PMC 6333487. PMID 30266559.
  13. Argenziano G, Ferrara G, Francione S, Di Nola K, Martino A, Zalaudek I (2009). "Dermoscopy--the ultimate tool for melanoma diagnosis". Semin Cutan Med Surg. 28 (3): 142–8. doi:10.1016/j.sder.2009.06.001. PMID 19782937.
  14. Argenziano G, Soyer HP, Chimenti S, Talamini R, Corona R, Sera F; et al. (2003). "Dermoscopy of pigmented skin lesions: results of a consensus meeting via the Internet". J Am Acad Dermatol. 48 (5): 679–93. doi:10.1067/mjd.2003.281. PMID 12734496.
  15. Menzies, Scott W.; Moloney, Fergal J.; Byth, Karen; Avramidis, Michelle; Argenziano, Giuseppe; Zalaudek, Iris; Braun, Ralph P.; Malvehy, Josep; Puig, Susana; Rabinovitz, Harold S.; Oliviero, Margaret; Cabo, Horacio; Bono, Riccardo; Pizzichetta, Maria A.; Claeson, Magdalena; Gaffney, Daniel C.; Soyer, H. Peter; Stanganelli, Ignazio; Scolyer, Richard A.; Guitera, Pascale; Kelly, John; McCurdy, Olivia; Llambrich, Alex; Marghoob, Ashfaq A.; Zaballos, Pedro; Kirchesch, Herbert M.; Piccolo, Domenico; Bowling, Jonathan; Thomas, Luc; Terstappen, Karin; Tanaka, Masaru; Pellacani, Giovanni; Pagnanelli, Gianluca; Ghigliotti, Giovanni; Ortega, Blanca Carlos; Crafter, Greg; Ortiz, Ana María Perusquía; Tromme, Isabelle; Karaarslan, Isil Kilinc; Ozdemir, Fezal; Tam, Anthony; Landi, Christian; Norton, Peter; Kaçar, Nida; Rudnicka, Lidia; Slowinska, Monika; Simionescu, Olga; Di Stefani, Alessandro; Coates, Elliot; Kreusch, Juergen (2013). "Dermoscopic Evaluation of Nodular Melanoma". JAMA Dermatology. 149 (6): 699. doi:10.1001/jamadermatol.2013.2466. ISSN 2168-6068.
  16. Phan A, Dalle S, Touzet S, Ronger-Savlé S, Balme B, Thomas L (2010). "Dermoscopic features of acral lentiginous melanoma in a large series of 110 cases in a white population". Br J Dermatol. 162 (4): 765–71. doi:10.1111/j.1365-2133.2009.09594.x. PMID 19922528.
  17. Steglich RB, Meotti CD, Ferreira MS, Lovatto L, de Carvalho AV, de Castro CG (2012). "Dermoscopic clues in the diagnosis of amelanotic and hypomelanotic malignant melanoma". An Bras Dermatol. 87 (6): 920–3. PMC 3699915. PMID 23197217.
  18. Witt C, Krengel S (2010). "Clinical and epidemiological aspects of subtypes of melanocytic nevi (Flat nevi, Miescher nevi, Unna nevi)". Dermatol Online J. 16 (1): 1. PMID 20137743.
  19. Bauer J, Garbe C (2003). "Acquired melanocytic nevi as risk factor for melanoma development. A comprehensive review of epidemiological data". Pigment Cell Res. 16 (3): 297–306. PMID 12753404.
  20. Granter SR, McKee PH, Calonje E, Mihm MC, Busam K (2001). "Melanoma associated with blue nevus and melanoma mimicking cellular blue nevus: a clinicopathologic study of 10 cases on the spectrum of so-called 'malignant blue nevus'". Am J Surg Pathol. 25 (3): 316–23. PMID 11224601.
  21. Luo S, Sepehr A, Tsao H (2011). "Spitz nevi and other Spitzoid lesions part I. Background and diagnoses". J Am Acad Dermatol. 65 (6): 1073–84. doi:10.1016/j.jaad.2011.04.040. PMC 3217183. PMID 22082838.
  22. Argenziano G, Agozzino M, Bonifazi E, Broganelli P, Brunetti B, Ferrara G; et al. (2011). "Natural evolution of Spitz nevi". Dermatology. 222 (3): 256–60. doi:10.1159/000326109. PMID 21494025.
  23. Pedrosa AF, Lopes JM, Azevedo F, Mota A (2016). "Spitz/Reed nevi: a review of clinical-dermatoscopic and histological correlation". Dermatol Pract Concept. 6 (2): 37–41. doi:10.5826/dpc.0602a07. PMC 4866625. PMID 27222770.
  24. Tanaka M, Sawada M, Kobayashi K (2011). "Key points in dermoscopic differentiation between lentigo maligna and solar lentigo". J Dermatol. 38 (1): 53–8. doi:10.1111/j.1346-8138.2010.01132.x. PMID 21175756.
  25. Sato T, Tanaka M (2014). "Linear sebaceous hyperplasia on the chest". Dermatol Pract Concept. 4 (1): 93–5. doi:10.5826/dpc.0401a16. PMC 3919849. PMID 24520522.
  26. Morgan MB, Stevens GL, Switlyk S (2005). "Benign lichenoid keratosis: a clinical and pathologic reappraisal of 1040 cases". Am J Dermatopathol. 27 (5): 387–92. PMID 16148406.

References