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Tumors of the Skin

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Atlas of Skin Disorders

Abstract

Skin tumor is the most intriguing topic for the clinicians. This chapter covers a wide range of issues and provides with informative clues and tips associated with clinical features and pathological presentations and keeps pace with the latest development in molecular biology and immunohistochemistry to assist the readers in the establishment of accurate diagnosis. These following disorders are elaborately selected and arranged from a histopathological perspective.

(1) Tumors of the epidermis include epidermal nevus, unilateral epidermal nevus, epidermal nevus syndrome, seborrheic keratosis, seborrheic keratosis and pityrosporum ovale, large cell acanthoma, giant cutaneous horn, multiple Bowen’s disease, extramammary Paget’s disease, eruptive keratoacanthoma, superficial basal cell carcinoma, fibroepithelioma of Pinkus, Marjolin’s ulcer of squamous cell carcinoma secondary to radiation, cutaneous clear cell squamous cell carcinoma, and milia en plaque.

(2) The list of cutaneous appendage proliferations and tumors present cases with eruptive vellus hair cysts, nevus comedonicus, dilated pore, inverted follicular keratosis, infundibulocystic basal cell carcinoma, trichofolliculoma, trichoepithelioma, bullous pilomatricoma, areolar sebaceous hyperplasia, nevus sebaceous with apocrine cystadenoma, linear nevus sebaceous syndrome, apocrine hidrocystoma, eccrine angiomatous hamartoma, syringocystadenoma papilliferum, eruptive milium-like syringoma, segmental multiple eccrine spiradenomas, clear cell hidradenoma, malignant eccrine poroma, or microcystic adnexal carcinoma.

(3) The category of cutaneous soft tissue proliferations and neoplasms introduces acquired digital fibrokeratoma, epithelioid cell histiocytoma, multiple eruptive dermatofibromas, intradermal nodular fasciitis, dermatofibrosarcoma protuberan, epithelioid sarcoma, superficial angiomyxoma, multicentric reticulohistiocytosis, Letterer-Siwe disease, cutaneous Rosai-Dorfman disease, phakomatosis pigmentovascularis, angiokeratoma corporis diffusum, angiokeratoma of Fordyce, angioma serpiginosum, reactive angioendotheliomatosis, epithelioid hemangioma, tufted angioma, verrucous hemangioma, targetoid hemosiderotic hemangioma, microvenular hemangioma, glomus tumor, spindle cell hemangioma, Kaposiform hemangioendothelioma, classic Kaposi’s sarcoma, cutaneous angiosarcoma, acquired progressive lymphangioma, lymphangioma, nevus lipomatosus superficialis, encephalocraniocutaneous lipomatosis, madelung disease, multiple leiomyoma, cutaneous leiomyosarcoma, subungual exostosis, and cutaneous endometriosis.

(4) Palisaded encapsulated neuroma, schwannoma, and cutaneous Merkel cell carcinoma belong to neural tumors.

(5) Melanocytic nevi and neoplasms include agminated Spitz nevus, subungual melanoma, fatal leptomeningeal melanoma in neurocutaneous melanosis, as well as rare forms of cutaneous melanoma.

(6) Cutaneous lymphoid proliferations and leukemic infiltration consist of cutaneous pseudolymphoma, Jessner’s lymphocytic infiltration of the skin Jessner, Ketron-Goodman disease, mycosis fungoides, erythrodermic cutaneous T-cell lymphoma, subcutaneous panniculitis-like T-cell lymphoma, hydroa vacciniforme-like lymphoma, extranodal NK-/T-cell lymphoma, primary cutaneous B-cell lymphoma, maculopapular cutaneous mastocytosis, diffuse cutaneous mastocytosis, mastocytoma, cutaneous plasmacytoma, polycythemia vera, leukemia cutis, and so on.

(7) Cutaneous metastases include cutaneous metastasis for lung cancer, cutaneous metastasis of gastrointestinal malignancy, Sister Mary Joseph’s nodule, and carcinoma en cuirasse.

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References

  1. Curth HO. Unilateral epidermal naevus resembling acanthosis nigricans. Br J Dermatol. 1976;95(4):433–6.

    Article  CAS  PubMed  Google Scholar 

  2. Khachemoune A, Janjua SA, Guldbakke KK. Inflammatory linear verrucous epidermal nevus: a case report and short review of the literature. Cutis. 2006;78(4):261–7.

    PubMed  Google Scholar 

  3. Zheng LQ, Huang Y, Qu YJ, Zhang YH, Han XC. Multiple basal cell carcinomas arising in a verrucous epidermal nevus. J Dermatol. 2013;40(6):482–3. https://doi.org/10.1111/1346-8138.12110.

    Article  PubMed  Google Scholar 

  4. Demetree JW, Lang PG, St Clair JT. Unilateral, linear, zosteriform epidermal nevus with acantholytic dyskeratosis. Arch Dermatol. 1979;115(7):875–7.

    Article  CAS  PubMed  Google Scholar 

  5. Ozcelik D, Parlak AH, Ozturk A, Kavak A, Celikel N. Unilateral linear verrucous epidermal nevus of the face and the oral mucosa. Plast Reconstr Surg. 2005;115(2):17e–9e.

    Article  PubMed  Google Scholar 

  6. Laura FS. Epidermal nevus syndrome. Handb Clin Neurol. 2013;111:349–68. https://doi.org/10.1016/B978-0-444-52891-9.00041-5.

    Article  PubMed  Google Scholar 

  7. Vujevich JJ, Mancini AJ. The epidermal nevus syndromes: multisystem disorders. J Am Acad Dermatol. 2004;50(6):957–61.

    Article  PubMed  Google Scholar 

  8. Goldberg LH, Collins SA, Siegel DM. The epidermal nevus syndrome: case report and review. Pediatr Dermatol. 1987;4(1):27–33.

    Article  CAS  PubMed  Google Scholar 

  9. Zhu WY. Multiple small papular seborrheic keratosis. Chin Med J. 1988;101(7):490–2.

    PubMed  CAS  Google Scholar 

  10. Li X, Zhu W. A case of seborrheic keratosis distributed along skin cleavage lines. J Dermatol. 1998;25(4):272–4.

    Article  CAS  PubMed  Google Scholar 

  11. Hafner C, Vogt T. Seborrheic keratosis. J Dtsch Dermatol Ges. 2008;6(8):664–77. https://doi.org/10.1111/j.1610-0387.2008.06788.x.

    Article  PubMed  Google Scholar 

  12. Bourlond A, Votion V, Armijo F, Minne G. Pityrosporum ovale in keratotic lesions of seborrheic areas. Ann Dermatol Venereol. 1984;111(12):1081–5.

    PubMed  CAS  Google Scholar 

  13. Sanchez Yus E, del Rio E, Requena L. Large-cell acanthoma is a distinctive condition. Am J Dermatopathol. 1992;14(2):140–7. discussion 148

    Article  CAS  PubMed  Google Scholar 

  14. Mehregan DR, Hamzavi F, Brown K. Large cell acanthoma. Int J Dermatol. 2003;42(1):36–9.

    Article  PubMed  Google Scholar 

  15. Yoon YH, Ju HJ, Lee KH, Park CJ. A cutaneous horn-like form of juvenile xanthogranuloma. Ann Dermatol. 2016;28(6):783–4. https://doi.org/10.5021/ad.2016.28.6.783.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Mantese SA, Diogo PM, Rocha A, Berbert AL, Ferreira AK, Ferreira TC. Cutaneous horn: a retrospective histopathological study of 222 cases. An Bras Dermatol. 2010;85(2):157–63.

    Article  PubMed  Google Scholar 

  17. Morton CA, Whitehurst C, McColl JH, Moore JV, MacKie RM. Photodynamic therapy for large or multiple patches of Bowen disease and basal cell carcinoma. Arch Dermatol. 2001;137(3):319–24.

    PubMed  CAS  Google Scholar 

  18. Murao K, Nakasuka A, Keyama T, Hashimoto I, Kubo Y. Case of multiple Bowen diseases associated with human papillomavirus type 16 in a patient with atopic dermatitis. J Dermatol. 2016;43(4):445–7. https://doi.org/10.1111/1346-8138.13216.

    Article  PubMed  Google Scholar 

  19. Kuniyuki S, Maekawa N. Ectopic extramammary Paget’s disease on the head: case report and literature review. Int J Dermatol. 2015;54(11):e483–6. https://doi.org/10.1111/ijd.13018.

    Article  PubMed  Google Scholar 

  20. Lloyd J, Flanagan AM. Mammary and extramammary Paget’s disease. J Clin Pathol. 2000;53(10):742–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Kwiek B, Schwartz RA. Keratoacanthoma (KA): an update and review. J Am Acad Dermatol. 2016;74(6):1220–33. https://doi.org/10.1016/j.jaad.2015.11.033.

    Article  PubMed  Google Scholar 

  22. Nofal A, Assaf M, Ghonemy S, Nofal E, Yosef A. Generalized eruptive keratoacanthoma: a diagnostic and therapeutic challenge. Int J Dermatol. 2015;54(2):160–7. https://doi.org/10.1111/ijd.12308.

    Article  PubMed  Google Scholar 

  23. Schwartz RA. Keratoacanthoma: a clinico-pathologic enigma. Dermatol Surg. 2004;30(2 Pt 2):326–33. discussion 333

    PubMed  Google Scholar 

  24. Handa Y, Kato Y, Ishikawa H, Tomita Y. Giant superficial basal cell carcinoma of the scrotum. Eur J Dermatol. 2005;15(3):186–8.

    PubMed  Google Scholar 

  25. Pyne JH, Myint E, Barr EM, Clark SP, David M, Na R, Hou R. Superficial basal cell carcinoma: a comparison of superficial only subtype with superficial combined with other subtypes by age, sex and anatomic site in 3150 cases. J Cutan Pathol. 2017;44:677–83. https://doi.org/10.1111/cup.12959.

    Article  PubMed  Google Scholar 

  26. Katona TM, Ravis SM, Perkins SM, Moores WB, Billings SD. Expression of androgen receptor by fibroepithelioma of Pinkus: evidence supporting classification as a basal cell carcinoma variant? Am J Dermatopathol. 2007;29(1):7–12. https://doi.org/10.1097/01.dad.0000245201.59762.d2.

    Article  PubMed  Google Scholar 

  27. Park MY, Kim YC. Fibroepithelioma of Pinkus: poor response to topical photodynamic therapy. Eur J Dermatol. 2010;20(1):133–4. https://doi.org/10.1684/ejd.2010.0831.

    Article  PubMed  Google Scholar 

  28. Pavlovic S, Wiley E, Guzman G, Morris D, Braniecki M. Marjolin ulcer: an overlooked entity. Int Wound J. 2011;8(4):419–24. https://doi.org/10.1111/j.1742-481X.2011.00811.x.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Reich-Schupke S, Doerler M, Wollina U, Dissemond J, Horn T, Strolin A, Erfurt-Berge C, Stucker M. Squamous cell carcinomas in chronic venous leg ulcers. Data of the German Marjolin Registry and review. J Dtsch Dermatol Ges. 2015;13(10):1006–13. https://doi.org/10.1111/ddg.12649.

    Article  PubMed  Google Scholar 

  30. Al-Arashi MY, Byers HR. Cutaneous clear cell squamous cell carcinoma in situ: clinical, histological and immunohistochemical characterization. J Cutan Pathol. 2007;34(3):226–33. https://doi.org/10.1111/j.1600-0560.2006.00593.x.

    Article  PubMed  Google Scholar 

  31. Misago N, Toda S, Narisawa Y. Tricholemmoma and clear cell squamous cell carcinoma (associated with Bowen’s disease): immunohistochemical profile in comparison to normal hair follicles. Am J Dermatopathol. 2012;34(4):394–9. https://doi.org/10.1097/DAD.0b013e318233f60a.

    Article  PubMed  Google Scholar 

  32. Barzegar M, Mozafari N. A new site of milia en plaque: report of a case and review of the literature. Int J Dermatol. 2015;54(12):1423–5. https://doi.org/10.1111/ijd.12364.

    Article  PubMed  Google Scholar 

  33. Ergin S, Basak P, Sari A. Milia en plaque. J Eur Acad Dermatol Venereol. 2000;14(1):47–9.

    Article  CAS  PubMed  Google Scholar 

  34. Martins LE, Werner B, Fonseca GP. Milia en plaque. An Bras Dermatol. 2010;85(6):895–8.

    Article  PubMed  Google Scholar 

  35. Torchia D, Vega J, Schachner LA. Eruptive vellus hair cysts: a systematic review. Am J Clin Dermatol. 2012;13(1):19–28. https://doi.org/10.2165/11589050-000000000-00000.

    Article  PubMed  Google Scholar 

  36. Shi G, Zhou Y, Cai YX, Li SJ, Fan YM. Clinicopathological features and expression of four keratins (K10, K14, K17 and K19) in six cases of eruptive vellus hair cysts. Clin Exp Dermatol. 2014;39(4):496–9. https://doi.org/10.1111/ced.12337.

    Article  PubMed  CAS  Google Scholar 

  37. Hong SD, Frieden IJ. Diagnosing eruptive vellus hair cysts. Pediatr Dermatol. 2001;18(3):258–9.

    Article  CAS  PubMed  Google Scholar 

  38. Tchernev G, Ananiev J, Semkova K, Dourmishev LA, Schonlebe J, Wollina U. Nevus comedonicus: an updated review. Dermatol Ther (Heidelb). 2013;3(1):33–40. https://doi.org/10.1007/s13555-013-0027-9.

    Article  Google Scholar 

  39. Ferrari B, Taliercio V, Restrepo P, Luna P, Abad ME, Larralde M. Nevus comedonicus: a case series. Pediatr Dermatol. 2015;32(2):216–9. https://doi.org/10.1111/pde.12466.

    Article  PubMed  Google Scholar 

  40. Moreira A, Menezes N, Guedes R, Tente D, Baptista A, Varela P. Dermoscopy of a dilated pore of Winer. Eur J Dermatol. 2010;20(2):229. https://doi.org/10.1684/ejd.2010.0852.

    Article  PubMed  Google Scholar 

  41. Resnik KS, Kantor GR, Howe NR, Ditre CM. Dilated pore nevus. A histologic variant of nevus comedonicus. Am J Dermatopathol. 1993;15(2):169–71.

    Article  CAS  PubMed  Google Scholar 

  42. Llambrich A, Zaballos P, Taberner R, Terrasa F, Banuls J, Pizarro A, Malvehy J, Puig S. Dermoscopy of inverted follicular keratosis: study of 12 cases. Clin Exp Dermatol. 2016;41(5):468–73. https://doi.org/10.1111/ced.12832.

    Article  PubMed  CAS  Google Scholar 

  43. Mehregan AH. Inverted follicular keratosis is a distinct follicular tumor. Am J Dermatopathol. 1983;5(5):467–70.

    Article  CAS  PubMed  Google Scholar 

  44. Honarpisheh H, Glusac EJ, Ko CJ. Cytokeratin 20 expression in basaloid follicular hamartoma and infundibulocystic basal cell carcinoma. J Cutan Pathol. 2014;41(12):916–21. https://doi.org/10.1111/cup.12410.

    Article  PubMed  Google Scholar 

  45. Kato N, Ueno H. Infundibulocystic basal cell carcinoma. Am J Dermatopathol. 1993;15(3):265–7.

    Article  CAS  PubMed  Google Scholar 

  46. Romero-Perez D, Garcia-Bustinduy M, Cribier B. Clinicopathologic study of 90 cases of trichofolliculoma. J Eur Acad Dermatol Venereol. 2017;31(3):e141–2. https://doi.org/10.1111/jdv.13960.

    Article  PubMed  CAS  Google Scholar 

  47. Kallam AR, Satyanarayana MA, Aryasomayajula S, Krishna BA. Basal cell carcinoma developing from trichoepithelioma: review of three cases. J Clin Diagn Res. 2016;10(3):PD17–9. https://doi.org/10.7860/JCDR/2016/15432.7464.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  48. Liang YH, Gao M, Sun LD, Liu LJ, Cui Y, Yang S, Fan X, Wang J, Xiao FL, Zhang XJ. Two novel CYLD gene mutations in Chinese families with trichoepithelioma and a literature review of 16 families with trichoepithelioma reported in China. Br J Dermatol. 2005;153(6):1213–5. https://doi.org/10.1111/j.1365-2133.2005.06960.x.

    Article  PubMed  CAS  Google Scholar 

  49. Parren LJ, Munte K, Winnepenninckx V, van Geel M, Steijlen PM, Frank J, van Steensel MA. Clustered unilateral trichoepitheliomas indicate Type 1 segmental manifestation of multiple familial trichoepithelioma. Clin Exp Dermatol. 2016;41(6):682–4. https://doi.org/10.1111/ced.12856.

    Article  PubMed  CAS  Google Scholar 

  50. Fetil E, Soyal MC, Menderes A, Lebe B, Gunes AT, Ozkan S. Bullous appearance of pilomatricoma. Dermatol Surg. 2003;29(10):1066–7.

    PubMed  Google Scholar 

  51. Ozkaya DB, Su O, Taskin B, Tas B, Sar M, Onsun N. Bullous pilomatricoma. Eur J Dermatol. 2013;23(1):104–5. https://doi.org/10.1684/ejd.2012.1886.

    Article  PubMed  Google Scholar 

  52. Belinchon I, Aguilar A, Tardio J, Gallego MA. Areolar sebaceous hyperplasia: a case report. Cutis. 1996;58(1):63–4.

    PubMed  CAS  Google Scholar 

  53. Chiriac A, Moldovan C, Coros MF, Podoleanu C, Moncea D, Stolnicu S. Bilateral areolar sebaceous hyperplasia in a post-menopausal woman. Eur J Dermatol. 2016;26(3):299–300. https://doi.org/10.1684/ejd.2016.2739.

    Article  PubMed  Google Scholar 

  54. Tsuji T, Yamauchi R. Areolar sebaceous hyperplasia with a Fordyce’s spot-like lesion. J Dermatol. 1994;21(7):524–6.

    Article  CAS  PubMed  Google Scholar 

  55. Campbell JP, Solomon AR Jr, Woo TY. Apocrine cystadenoma arising in a nevus sebaceus of Jadassohn. Cutis. 1984;34(5):510–2.

    PubMed  CAS  Google Scholar 

  56. Kamyab-Hesari K, Seirafi H, Jahan S, Aghazadeh N, Hejazi P, Azizpour A, Goodarzi A. Nevus sebaceus: a clinicopathological study of 168 cases and review of the literature. Int J Dermatol. 2016;55(2):193–200. https://doi.org/10.1111/ijd.12845.

    Article  PubMed  Google Scholar 

  57. Hsu MC, Liau JY, Hong JL, Cheng Y, Liao YH, Chen JS, Sheen YS, Hong JB. Secondary neoplasms arising from nevus sebaceus: a retrospective study of 450 cases in Taiwan. J Dermatol. 2016;43(2):175–80. https://doi.org/10.1111/1346-8138.13070.

    Article  PubMed  Google Scholar 

  58. Lovejoy FH Jr, Boyle WE Jr. Linear nevus sebaceous syndrome: report of two cases and a review of the literature. Pediatrics. 1973;52(3):382–7.

    PubMed  Google Scholar 

  59. Menascu S, Donner EJ. Linear nevus sebaceous syndrome: case reports and review of the literature. Pediatr Neurol. 2008;38(3):207–10. https://doi.org/10.1016/j.pediatrneurol.2007.10.012.

    Article  PubMed  Google Scholar 

  60. Gilchrist HM, Wick MR, Patterson JW. Liesegang rings in an apocrine hidrocystoma: a case report and review of literature. J Cutan Pathol. 2010;37(10):1064–6. https://doi.org/10.1111/j.1600-0560.2010.01559.x.

    Article  PubMed  Google Scholar 

  61. Lopez V, Alonso V, Jorda E, Santonja N. Apocrine hidrocystoma on the penis of a 40-year-old man. Int J Dermatol. 2013;52(4):502–4. https://doi.org/10.1111/j.1365-4632.2011.04893.x.

    Article  PubMed  Google Scholar 

  62. Holcomb M, Sun G, Eldin K, Brandon K. Verrucous hyperpigmented plaque in a 15-month-old boy. Eccrine angiomatous hamartoma (EAH) associated with verrucous hemangioma (VH). Int J Dermatol. 2013;52(1):25–6. https://doi.org/10.1111/j.1365-4632.2012.05690.x.

    Article  PubMed  Google Scholar 

  63. Patterson AT, Kumar MG, Bayliss SJ, Witman PM, Dehner LP, Gru AA. Eccrine angiomatous hamartoma: a clinicopathologic review of 18 cases. Am J Dermatopathol. 2016;38(6):413–7. https://doi.org/10.1097/DAD.0000000000000430.

    Article  PubMed  Google Scholar 

  64. Dufrechou L, Acosta A, Beltramo P, Pomies V, Caruso R, Salmenton GM, Alvarez M. Syringocystadenoma papilliferum arising on the scrotum. Pediatr Dermatol. 2013;30(3):e12–3. https://doi.org/10.1111/j.1525-1470.2012.01768.x.

    Article  PubMed  Google Scholar 

  65. Kasashima S, Kawashima A, Fujii T. Syringocystadenoma papilliferum of the male nipple. J Cutan Pathol. 2016;43(8):679–83. https://doi.org/10.1111/cup.12593.

    Article  PubMed  Google Scholar 

  66. Philipone E, Chen S. Unique case: syringocystadenoma papilliferum associated with an eccrine nevus. Am J Dermatopathol. 2009;31(8):806–7. https://doi.org/10.1097/DAD.0b013e31819abe12.

    Article  PubMed  Google Scholar 

  67. Tatsuno K, Yagi H, Tokura Y. Eruptive milium-like syringoma showing eccrine duct origin of milia. J Dermatol. 2012;39(10):878–9. https://doi.org/10.1111/j.1346-8138.2011.01444.x.

    Article  PubMed  Google Scholar 

  68. Zhong P, Tan C. Dermoscopic features of eruptive milium-like syringoma. Eur J Dermatol. 2015;25(2):203–4. https://doi.org/10.1684/ejd.2014.2506.

    Article  PubMed  Google Scholar 

  69. Ren F, Hu Z, Kong Q, Sang H. Multiple segmental eccrine spiradenoma with a zosteriform pattern: a case report and literature review. Ann Dermatol. 2015;27(4):435–8. https://doi.org/10.5021/ad.2015.27.4.435.

    Article  PubMed  PubMed Central  Google Scholar 

  70. Rodriguez-Martin M, Sanchez Gonzalez R, Saez-Rodriguez M, Garcia-Bustinduy M, Martin-Herrera A, Noda-Cabrera A. An unusual case of congenital linear eccrine spiradenoma. Pediatr Dermatol. 2009;26(2):180–3. https://doi.org/10.1111/j.1525-1470.2009.00879.x.

    Article  PubMed  Google Scholar 

  71. Yoshida A, Sato T, Sugawara Y, Matsuta M, Akasaka T. Two cases of multiple eccrine spiradenoma with linear or localized formation. J Dermatol. 2004;31(7):564–8.

    Article  PubMed  Google Scholar 

  72. Au B, Sidiropoulos KG, Ghazarian D, Sidiropoulos M. Lymph node involvement by a clear cell nodular hidradenoma-like tumor of uncertain malignant potential. Am J Dermatopathol. 2017;39:953–4. https://doi.org/10.1097/DAD.0000000000000808.

    Article  PubMed  Google Scholar 

  73. Gilaberte Y, Grasa MP, Carapeto FJ. Clear cell hidradenoma. J Am Acad Dermatol. 2006;54(5 Suppl):248–9. https://doi.org/10.1016/j.jaad.2006.03.003.

    Article  PubMed  Google Scholar 

  74. Yu G, Goodloe S Jr, D’Angelis CA, McGrath BE, Chen F. Giant clear cell hidradenoma of the knee. J Cutan Pathol. 2010;37(9):e37–41. https://doi.org/10.1111/j.1600-0560.2009.01354.x.

    Article  PubMed  Google Scholar 

  75. Pena J, Suster S. Squamous differentiation in malignant eccrine poroma. Am J Dermatopathol. 1993;15(5):492–6.

    Article  CAS  PubMed  Google Scholar 

  76. Perna C, Cuevas J, Jimenez-Heffernan JA, Hardisson D, Contreras F. Eccrine porocarcinoma (malignant eccrine poroma). Am J Surg Pathol. 2002;26(2):272–4.

    Article  PubMed  Google Scholar 

  77. Sawaya JL, Khachemoune A. Poroma: a review of eccrine, apocrine, and malignant forms. Int J Dermatol. 2014;53(9):1053–61. https://doi.org/10.1111/ijd.12448.

    Article  PubMed  Google Scholar 

  78. Chen J, Yang S, Chen J, Liao T, Deng W, Li W. Microcystic adnexal carcinoma in a non-Caucasian patient: a case report and review of the literature. Oncol Lett. 2016;11(4):2471–4. https://doi.org/10.3892/ol.2016.4242.

    Article  PubMed  PubMed Central  Google Scholar 

  79. Jfri A, Al Hawsawi K, Marghalani S, Alkhuzaie A. Microcystic adnexal carcinoma: unusual presentation. J Eur Acad Dermatol Venereol. 2016;30(1):165–7. https://doi.org/10.1111/jdv.12659.

    Article  PubMed  CAS  Google Scholar 

  80. McKinley LH, Seastrom S, Hanly AJ, Miller RA. Microcystic adnexal carcinoma: review of a potential diagnostic pitfall and management. Cutis. 2014;93(3):162–5.

    PubMed  Google Scholar 

  81. Baykal C, Buyukbabani N, Yazganoglu KD, Saglik E. Acquired digital fibrokeratoma. Cutis. 2007;79(2):129–32.

    PubMed  Google Scholar 

  82. Berger RS, Spielvogel RL. Dermal papule on a distal digit. Acquired digital fibrokeratoma. Arch Dermatol. 1988;124(10):1559–60. 1562–3

    Article  CAS  PubMed  Google Scholar 

  83. Jang MS, Kang DY, Park JB, Kang JS, Baek JW, Kim ST, Suh KS. Epithelioid cell histiocytoma: broad differential diagnostic considerations. J Dermatol. 2012;39(6):579–81. https://doi.org/10.1111/j.1346-8138.2011.01429.x.

    Article  PubMed  Google Scholar 

  84. Manente L, Schmitt I, Onetti AM, Peris K, Caracciolo E, Chimenti S. Cutaneous epithelioid cell histiocytoma: immunohistochemical and ultrastructural findings suggesting endothelial origin. Am J Dermatopathol. 1997;19(5):519–23.

    Article  CAS  PubMed  Google Scholar 

  85. Mehregan AH, Mehregan DR, Broecker A. Epithelioid cell histiocytoma. A clinicopathologic and immunohistochemical study of eight cases. J Am Acad Dermatol. 1992;26(2 Pt 1):243–6.

    Article  CAS  PubMed  Google Scholar 

  86. Alexandrescu DT, Wiernik PH. Multiple eruptive dermatofibromas occurring in a patient with chronic myelogenous leukemia. Arch Dermatol. 2005;141(3):397–8. https://doi.org/10.1001/archderm.141.3.397.

    Article  PubMed  Google Scholar 

  87. Llamas-Velasco M, Fraga J, Solano-Lopez GE, Steegmann JL, Garcia Diez A, Requena L. Multiple eruptive dermatofibromas related to imatinib treatment. J Eur Acad Dermatol Venereol. 2014;28(7):979–81. https://doi.org/10.1111/jdv.12328.

    Article  PubMed  CAS  Google Scholar 

  88. Veraldi S, Bocor M, Gianotti R, Gasparini G. Multiple eruptive dermatofibromas localized exclusively to the buttock. Int J Dermatol. 1991;30(7):507–8.

    Article  CAS  PubMed  Google Scholar 

  89. de Feraudy S, Fletcher CD. Intradermal nodular fasciitis: a rare lesion analyzed in a series of 24 cases. Am J Surg Pathol. 2010;34(9):1377–81. https://doi.org/10.1097/PAS.0b013e3181ed7374.

    Article  PubMed  Google Scholar 

  90. Terai M, Oka M, Kunisada M, Kawakami F, Nishigori C. Intradermal nodular fasciitis. Eur J Dermatol. 2012;22(2):285–6. https://doi.org/10.1684/ejd.2012.1657.

    Article  PubMed  Google Scholar 

  91. Buck DW 2nd, Kim JY, Alam M, Rawlani V, Johnson S, Connor CM, Dumanian GA, Wayne JD. Multidisciplinary approach to the management of dermatofibrosarcoma protuberans. J Am Acad Dermatol. 2012;67(5):861–6. https://doi.org/10.1016/j.jaad.2012.01.039.

    Article  PubMed  Google Scholar 

  92. Kuzel P, Mahmood MN, Metelitsa AI, Salopek TG. A clinicopathologic review of a case series of dermatofibrosarcoma protuberans with fibrosarcomatous differentiation. J Cutan Med Surg. 2015;19(1):28–34. https://doi.org/10.2310/7750.2014.13192.

    Article  PubMed  Google Scholar 

  93. Thway K, Noujaim J, Jones RL, Fisher C. Dermatofibrosarcoma protuberans: pathology, genetics, and potential therapeutic strategies. Ann Diagn Pathol. 2016;25:64–71. https://doi.org/10.1016/j.anndiagpath.2016.09.013.

    Article  PubMed  Google Scholar 

  94. Halling AC, Wollan PC, Pritchard DJ, Vlasak R, Nascimento AG. Epithelioid sarcoma: a clinicopathologic review of 55 cases. Mayo Clin Proc. 1996;71(7):636–42. https://doi.org/10.1016/S0025-6196(11)63000-0.

    Article  PubMed  CAS  Google Scholar 

  95. Jamshidi F, Bashashati A, Shumansky K, Dickson B, Gokgoz N, Wunder JS, Andrulis IL, Lazar AJ, Shah SP, Huntsman DG, Nielsen TO. The genomic landscape of epithelioid sarcoma cell lines and tumours. J Pathol. 2016;238(1):63–73. https://doi.org/10.1002/path.4636.

    Article  PubMed  CAS  Google Scholar 

  96. Sobanko JF, Meijer L, Nigra TP. Epithelioid sarcoma: a review and update. J Clin Aesthet Dermatol. 2009;2(5):49–54.

    PubMed  PubMed Central  Google Scholar 

  97. Basak S, Rogers S, Solomonsz AF. Superficial angiomyxoma of the vulva: a case report of a rare cutaneous tumour. J Obstet Gynaecol. 2011;31(4):360–1. https://doi.org/10.3109/01443615.2011.554612.

    Article  PubMed  CAS  Google Scholar 

  98. Falidas E, Rallis E, Vlachos C, Konstantoudakis S, Villias C. Superficial subungual angiomyxoma: case report and review of the literature. J Cutan Med Surg. 2011;15(3):180–2. https://doi.org/10.2310/7750.2011.10036.

    Article  PubMed  Google Scholar 

  99. Cyrulnik AA, Paz KB, Amin B, Mann RE, Krishnamurthy K, Friedman AJ. Multicentric reticulohistiocytosis: contrasting presentations in 2 Hispanic patients. Cutis. 2014;93(5):243–6.

    PubMed  Google Scholar 

  100. Kandiah DA. Multicentric reticulohistiocytosis. Mayo Clin Proc. 2014;89(8):e73. https://doi.org/10.1016/j.mayocp.2013.10.036.

    Article  PubMed  Google Scholar 

  101. Selmi C, Greenspan A, Huntley A, Gershwin ME. Multicentric reticulohistiocytosis: a critical review. Curr Rheumatol Rep. 2015;17(6):511. https://doi.org/10.1007/s11926-015-0511-6.

    Article  PubMed  Google Scholar 

  102. Tajirian AL, Malik MK, Robinson-Bostom L, Lally EV. Multicentric reticulohistiocytosis. Clin Dermatol. 2006;24(6):486–92. https://doi.org/10.1016/j.clindermatol.2006.07.010.

    Article  PubMed  Google Scholar 

  103. Kuttner BJ, Friedman KJ, Burton CS 3rd, Olsen EA. Letterer-Siwe disease in an adult. Cutis. 1987;39(2):142–6.

    PubMed  CAS  Google Scholar 

  104. Wright AL, Tucker WF, Slater DN, Harrington CI. Letterer-Siwe disease in the ninth decade. J Am Acad Dermatol. 1985;12(2 Pt 1):369–71.

    Article  CAS  PubMed  Google Scholar 

  105. Kutlubay Z, Bairamov O, Sevim A, Demirkesen C, Mat MC. Rosai-Dorfman disease: a case report with nodal and cutaneous involvement and review of the literature. Am J Dermatopathol. 2014;36(4):353–7. https://doi.org/10.1097/DAD.0b013e31829e5564.

    Article  PubMed  Google Scholar 

  106. Pitamber HV, Grayson W. Five cases of cutaneous Rosai-Dorfman disease. Clin Exp Dermatol. 2003;28(1):17–21.

    Article  CAS  PubMed  Google Scholar 

  107. Al Robaee A, Banka N, Alfadley A. Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome. Pediatr Dermatol. 2004;21(6):642–5. https://doi.org/10.1111/j.0736-8046.2004.21605.x.

    Article  PubMed  Google Scholar 

  108. Namiki T, Takahashi M, Nojima K, Ueno M, Hanafusa T, Tokoro S, Yokozeki H. Phakomatosis pigmentovascularis type IIb: a case with Klippel-Trenaunay syndrome and extensive dermal melanocytosis as nevus of Ota, nevus of Ito and ectopic Mongolian spots. J Dermatol. 2017;44(3):e32–3. https://doi.org/10.1111/1346-8138.13505.

    Article  PubMed  Google Scholar 

  109. Fimiani M, Mazzatenta C, Rubegni P, Andreassi L. Idiopathic angiokeratoma corporis diffusum. Clin Exp Dermatol. 1997;22(4):205–6.

    Article  CAS  PubMed  Google Scholar 

  110. Molho-Pessach V, Bargal R, Abramowitz Y, Doviner V, Ingber A, Raas-Rothschild A, Ne’eman Z, Zeigler M, Zlotogorski A. Angiokeratoma corporis diffusum in human beta-mannosidosis: report of a new case and a novel mutation. J Am Acad Dermatol. 2007;57(3):407–12. https://doi.org/10.1016/j.jaad.2007.01.037.

    Article  PubMed  Google Scholar 

  111. Ghosh SK, Ghosh S, Agarwal M. Multiple giant angiokeratoma of Fordyce on the shaft of the penis masquerading as keratoacanthoma. An Bras Dermatol. 2015;90(3 Suppl 1):150–2. https://doi.org/10.1590/abd1806-4841.20153876.

    Article  PubMed  PubMed Central  Google Scholar 

  112. Gioglio L, Porta C, Moroni M, Nastasi G, Gangarossa I. Scrotal angiokeratoma (Fordyce): histopathological and ultrastructural findings. Histol Histopathol. 1992;7(1):47–55.

    PubMed  CAS  Google Scholar 

  113. Duman N, Ersoy-Evans S. Angioma serpiginosum: report of two cases suggesting type 1 mosaicism and proposal of adding it to the list of mosaic skin conditions. Int J Dermatol. 2015;54(3):e88–9. https://doi.org/10.1111/ijd.12710.

    Article  PubMed  Google Scholar 

  114. Kalisiak MS, Haber RM. Angioma serpiginosum with linear distribution: case report and review of the literature. J Cutan Med Surg. 2008;12(4):180–3. https://doi.org/10.2310/7750.2008.07039.

    Article  PubMed  Google Scholar 

  115. Kirke S, Angus B, Kesteven PJ, Calonje E, Simpson N. Localized reactive angioendotheliomatosis. Clin Exp Dermatol. 2007;32(1):45–7. https://doi.org/10.1111/j.1365-2230.2006.02254.x.

    Article  PubMed  CAS  Google Scholar 

  116. Mayor-Ibarguren A, Gomez-Fernandez C, Beato-Merino MJ, Gonzalez-Ramos J, Rodriguez-Bandera AI, Herranz-Pinto P. Diffuse reactive angioendotheliomatosis secondary to the administration of trabectedin and pegfilgrastim. Am J Dermatopathol. 2015;37(7):581–4. https://doi.org/10.1097/DAD.0000000000000160.

    Article  PubMed  Google Scholar 

  117. Cham E, Smoller BR, Lorber DA, Victor TA, Cibull TL. Epithelioid hemangioma (angiolymphoid hyperplasia with eosinophilia) arising on the extremities. J Cutan Pathol. 2010;37(10):1045–52. https://doi.org/10.1111/j.1600-0560.2009.01400.x.

    Article  PubMed  Google Scholar 

  118. Kanik AB, Oh CH, Bhawan J. Disseminated cutaneous epithelioid hemangioma. J Am Acad Dermatol. 1996;35(5 Pt 2):851–3.

    Article  CAS  PubMed  Google Scholar 

  119. Ma HJ, Zhao G, Li Y, Li DG. Tufted angioma presented with segmental hyperpigmented plaque in a young Chinese woman. J Dermatol. 2010;37(2):190–2. https://doi.org/10.1111/j.1346-8138.2009.00747.x.

    Article  PubMed  Google Scholar 

  120. Tasani M, Ancliff P, Glover M. Sirolimus therapy for children with problematic Kaposiform haemangioendothelioma and tufted angioma. Br J Dermatol. 2017. https://doi.org/10.1111/bjd.15640.

  121. Wang L, Liu L, Wang G, Gao T. Congenital disseminated tufted angioma. J Cutan Pathol. 2013;40(4):405–8. https://doi.org/10.1111/cup.12089.

    Article  PubMed  Google Scholar 

  122. Tennant LB, Mulliken JB, Perez-Atayde AR, Kozakewich HP. Verrucous hemangioma revisited. Pediatr Dermatol. 2006;23(3):208–15. https://doi.org/10.1111/j.1525-1470.2006.00219.x.

    Article  PubMed  Google Scholar 

  123. Wang L, Gao T, Wang G. Verrucous hemangioma: a clinicopathological and immunohistochemical analysis of 74 cases. J Cutan Pathol. 2014;41(11):823–30. https://doi.org/10.1111/cup.12385.

    Article  PubMed  Google Scholar 

  124. Kakizaki P, Valente NY, Paiva DL, Dantas FL, Goncalves SV. Targetoid hemosiderotic hemangioma—case report. An Bras Dermatol. 2014;89(6):956–9.

    Article  PubMed  PubMed Central  Google Scholar 

  125. Mentzel T, Partanen TA, Kutzner H. Hobnail hemangioma (“targetoid hemosiderotic hemangioma”): clinicopathologic and immunohistochemical analysis of 62 cases. J Cutan Pathol. 1999;26(6):279–86.

    Article  CAS  PubMed  Google Scholar 

  126. Kim YC, Park HJ, Cinn YW. Microvenular hemangioma. Dermatology. 2003;206(2):161–4. https://doi.org/10.1159/000068453.

    Article  PubMed  Google Scholar 

  127. Napekoski KM, Fernandez AP, Billings SD. Microvenular hemangioma: a clinicopathologic review of 13 cases. J Cutan Pathol. 2014;41(11):816–22. https://doi.org/10.1111/cup.12386.

    Article  PubMed  Google Scholar 

  128. Gencoglan G, Dereli T, Kazandi AC. Subungual glomus tumor: surgical and histopathologic evaluation. Cutan Ocul Toxicol. 2011;30(1):72–4. https://doi.org/10.3109/15569527.2010.521224.

    Article  PubMed  Google Scholar 

  129. Sandoval M, Carrasco-Zuber J, Gonzalez S. Extradigital symplastic glomus tumor of the hand: report of 2 cases and literature review. Am J Dermatopathol. 2015;37(7):560–2. https://doi.org/10.1097/DAD.0000000000000132.

    Article  PubMed  Google Scholar 

  130. Coras B, Hohenleutner U, Landthaler M, Hohenleutner S. Spindle cell hemangioma. Dermatol Surg. 2003;29(8):875–8.

    PubMed  Google Scholar 

  131. Wang L, Gao T, Wang G. Expression of Prox1, D2-40, and WT1 in spindle cell hemangioma. J Cutan Pathol. 2014;41(5):447–50. https://doi.org/10.1111/cup.12309.

    Article  PubMed  Google Scholar 

  132. Cyrulnik AA, Dawkins MC, Smalberger GJ, Young S, Mann RE, Jacobson MI, Friedman AJ. Kaposiform hemangioendothelioma with Kasabach-Merritt syndrome mistaken for child abuse in a newborn. Cutis. 2014;93(3):E17–20.

    PubMed  Google Scholar 

  133. Reichel A, Hamm H, Wiegering V, Wiewrodt B, Neubauer H, Ernestus K, Winkler B. Kaposiform hemangioendothelioma with Kasabach-Merritt syndrome: successful treatment with sirolimus. J Dtsch Dermatol Ges. 2017;15(3):329–31. https://doi.org/10.1111/ddg.12987.

    Article  PubMed  Google Scholar 

  134. Almohideb M, Watters AK, Gerstein W. Familial classic Kaposi sarcoma in two siblings: case report and literature review. J Cutan Med Surg. 2013;17(5):356–61. https://doi.org/10.2310/7750.2013.12082.

    Article  PubMed  Google Scholar 

  135. Scott B, Griffin JR. Lymphangioma-like classic Kaposi sarcoma. Int J Dermatol. 2017;56(6):e141–2. https://doi.org/10.1111/ijd.13552.

    Article  PubMed  Google Scholar 

  136. Dhanasekar P, Karthikeyan VS, Rajkumar N, Chandra Sistla S, Manwar Ali S, Basu D, Malathi M. Cutaneous angiosarcoma of the scalp masquerading as a squamous cell carcinoma: case report and literature review. J Cutan Med Surg. 2012;16(3):187–90. https://doi.org/10.1177/120347541201600309.

    Article  PubMed  Google Scholar 

  137. Lu Y, Zhang M. Pemphigus herpetiformis in a patient with well‐differentiated cutaneous angiosarcoma: Case report and review of the published work. The Journal of Dermatology. 2012;39(1):89–91. https://doi.org/10.1111/j.1346-8138.2011.01287.x.

    Article  CAS  PubMed  Google Scholar 

  138. Kim HS, Kim JW, Yu DS. Acquired progressive lymphangioma. J Eur Acad Dermatol Venereol. 2007;21(3):416–7. https://doi.org/10.1111/j.1468-3083.2006.01904.x.

    Article  PubMed  CAS  Google Scholar 

  139. Zhu JW, Lu ZF, Zheng M. Acquired progressive lymphangioma in the inguinal area mimicking giant condyloma acuminatum. Cutis. 2014;93(6):316–9.

    PubMed  Google Scholar 

  140. Zhu WY, Penneys NS, Reyes B, Khatib Z, Schachner L. Acquired progressive lymphangioma. J Am Acad Dermatol. 1991;24(5 Pt 2):813–5.

    Article  CAS  PubMed  Google Scholar 

  141. Chang MB, Newman CC, Davis MD, Lehman JS. Acquired lymphangiectasia (lymphangioma circumscriptum) of the vulva: clinicopathologic study of 11 patients from a single institution and 67 from the literature. Int J Dermatol. 2016;55(9):e482–7. https://doi.org/10.1111/ijd.13264.

    Article  PubMed  Google Scholar 

  142. Goyal M, Wankhade VH, Mukhi JI, Singh RP. Nevus lipomatosus cutaneous superficialis—a rare hamartoma: report of two cases. J Clin Diagn Res. 2016;10(10):WD01–2. https://doi.org/10.7860/JCDR/2016/19126.8595.

    Article  PubMed  PubMed Central  Google Scholar 

  143. Mansur AT, Yasar S, Aydingoz IE, Goktay F, Ozdemir N, Sungurlu F. Colocalization of lipedematous scalp and nevus lipomatosus superficialis: a case report. J Cutan Pathol. 2007;34(4):342–5. https://doi.org/10.1111/j.1600-0560.2006.00610.x.

    Article  PubMed  Google Scholar 

  144. Kim DH, Park SB, Lee Y, Im M, Seo YJ, Choi SH, Lee JH. Encephalocraniocutaneous lipomatosis without neurologic anomalies. Ann Dermatol. 2012;24(4):476–8. https://doi.org/10.5021/ad.2012.24.4.476.

    Article  PubMed  PubMed Central  Google Scholar 

  145. Gawel J, Schwartz RA, Jozwiak S. Encephalocraniocutaneous lipomatosis. J Cutan Med Surg. 2003;7(1):61–5. https://doi.org/10.1177/120347540300700111.

    Article  PubMed  Google Scholar 

  146. Chen HW, Chen HW, Chen HL, Lai CC. Madelung disease. Am J Med Sci. 2016;352(6):654. https://doi.org/10.1016/j.amjms.2016.06.009.

    Article  PubMed  Google Scholar 

  147. Tan O, Ergen D. Madelung syndrome with pubic involvement. Dermatol Surg. 2008;34(6):811–4. https://doi.org/10.1111/j.1524-4725.2008.34152.x.

    Article  PubMed  CAS  Google Scholar 

  148. Gokdemir G, Sakiz D, Koslu A. Multiple cutaneous leiomyomas of the nipple. J Eur Acad Dermatol Venereol. 2006;20(4):468–9. https://doi.org/10.1111/j.1468-3083.2006.01451.x.

    Article  PubMed  CAS  Google Scholar 

  149. Gravvanis A, Kakagia D, Papadopoulos S, Tsoutsos D. Dermal skin template for the management of multiple cutaneous leiomyomas. J Cutan Med Surg. 2009;13(2):102–5. https://doi.org/10.2310/7750.2008.07074.

    Article  PubMed  Google Scholar 

  150. Berzal-Cantalejo F, Sabater-Marco V, Perez-Valles A, Martorell-Cebollada M. Desmoplastic cutaneous leiomyosarcoma: case report and review of the literature. J Cutan Pathol. 2006;33(Suppl 2):29–31. https://doi.org/10.1111/j.1600-0560.2006.00542.x.

    Article  PubMed  Google Scholar 

  151. De Giorgi V, Sestini S, Massi D, Papi F, Alfaioli B, Lotti T. Superficial cutaneous leiomyosarcoma: a rare, misleading tumor. Am J Clin Dermatol. 2008;9(3):185–7.

    Article  PubMed  Google Scholar 

  152. Weiler L, Poulalhon N, Slama A, Guillaud-Bataille M, Thomas L. Isolated cutaneous leiomyosarcoma revealing a novel germline mutation of the fumarate hydratase gene. Br J Dermatol. 2016;175(5):1104–6. https://doi.org/10.1111/bjd.13867.

    Article  PubMed  CAS  Google Scholar 

  153. Ilyas W, Geskin L, Joseph AK, Seraly MP. Subungual exostosis of the third toe. J Am Acad Dermatol. 2001;45(6 Suppl):S200–1.

    Article  CAS  PubMed  Google Scholar 

  154. Russell JD, Nance K, Nunley JR, Maher IA. Subungual exostosis. Cutis. 2016;98(2):128–9.

    PubMed  Google Scholar 

  155. Farooq U, Laureano AC, Miteva M, Elgart GW. Cutaneous endometriosis: diagnostic immunohistochemistry and clinicopathologic correlation. J Cutan Pathol. 2011;38(6):525–8. https://doi.org/10.1111/j.1600-0560.2011.01681.x.

    Article  PubMed  Google Scholar 

  156. Fernandez Vozmediano JM, Armario Hita JC, Cuevas Santos J. Cutaneous endometriosis. Int J Dermatol. 2010;49(12):1410–2. https://doi.org/10.1111/j.1365-4632.2010.04585.x.

    Article  PubMed  CAS  Google Scholar 

  157. Lee MS, Lee JD, Cho SH, Kim HS. Palisaded encapsulated neuroma in a zosteriform distribution. Indian J Dermatol. 2016;61(1):126. https://doi.org/10.4103/0019-5154.174173.

    Article  PubMed  PubMed Central  Google Scholar 

  158. Megahed M. Palisaded encapsulated neuroma (solitary circumscribed neuroma). A clinicopathologic and immunohistochemical study. Am J Dermatopathol. 1994;16(2):120–5.

    Article  CAS  PubMed  Google Scholar 

  159. Kneitz H, Weyandt G, Meissner C, Gebhart E, Brocker EB. Dermal schwannoma (neurilemmoma): a peculiar foreign body reaction? Am J Dermatopathol. 2010;32(4):367–9. https://doi.org/10.1097/DAD.0b013e3181bb1972.

    Article  PubMed  Google Scholar 

  160. Moon SE, Cho YJ, Kwon OS. Subungual schwannoma: a rare location. Dermatol Surg. 2005;31(5):592–4.

    Article  CAS  PubMed  Google Scholar 

  161. Mendenhall WM, Kirwan JM, Morris CG, Amdur RJ, Werning JW, Mendenhall NP. Cutaneous Merkel cell carcinoma. Am J Otolaryngol. 2012;33(1):88–92. https://doi.org/10.1016/j.amjoto.2011.02.003.

    Article  PubMed  Google Scholar 

  162. Sparks J, Sparks M, Malone JC. Cutaneous Merkel cell carcinoma: multiple asynchronous primary lesions in a patient on immunosuppressive therapy. J Cutan Pathol. 2017;44(3):309–12. https://doi.org/10.1111/cup.12860.

    Article  PubMed  Google Scholar 

  163. Aloi F, Tomasini C, Pippione M. Agminated Spitz nevi occurring within a congenital speckled lentiginous nevus. Am J Dermatopathol. 1995;17(6):594–8.

    Article  CAS  PubMed  Google Scholar 

  164. Pontoizeau J, Stefan A, Comoz F, Houlier A, Haddad V, Pissaloux D, de la Fouchardiere A. Agminated Spitz nevus arising in normal skin with redundant HRAS mutation. Eur J Dermatol. 2017;27(1):73–4. https://doi.org/10.1684/ejd.2016.2894.

    Article  PubMed  Google Scholar 

  165. Kato T, Suetake T, Sugiyama Y, Tabata N, Tagami H. Epidemiology and prognosis of subungual melanoma in 34 Japanese patients. Br J Dermatol. 1996;134(3):383–7.

    Article  CAS  PubMed  Google Scholar 

  166. Sone Y, Namiki T, Munetsugu T, Ueno M, Tokoro S, Nishizawa A, Takayama K, Yokozeki H. A case of subungual melanoma with bone invasion: destructive local invasion and multiple skin metastases. J Eur Acad Dermatol Venereol. 2016;30(6):1049–50. https://doi.org/10.1111/jdv.13102.

    Article  PubMed  CAS  Google Scholar 

  167. Alikhan A, Ibrahimi OA, Eisen DB. Congenital melanocytic nevi: where are we now? Part I. Clinical presentation, epidemiology, pathogenesis, histology, malignant transformation, and neurocutaneous melanosis. J Am Acad Dermatol. 2012;67(4):495.e1–17quiz 512–494. https://doi.org/10.1016/j.jaad.2012.06.023.

    Article  Google Scholar 

  168. Furtado S, Furtado SV, Ghosal N, Hegde AS. Fatal leptomeningeal melanoma in neurocutaneous melanosis. Pediatr Dermatol. 2012;29(3):358–61. https://doi.org/10.1111/j.1525-1470.2011.01424.x.

    Article  PubMed  Google Scholar 

  169. Matsumura M, Okudela K, Tateishi Y, Umeda S, Mitsui H, Suzuki T, Nakayama T, Inayama Y, Ohashi K. Leptomeningeal melanomatosis associated with neurocutaneous melanosis: an autopsy case report. Pathol Int. 2015;65(2):100–5. https://doi.org/10.1111/pin.12238.

    Article  PubMed  CAS  Google Scholar 

  170. Asgari MM, Shen L, Sokil MM, Yeh I, Jorgenson E. Prognostics factors and survival in acral lentiginous melanoma. Br J Dermatol. 2017;177:428–35. https://doi.org/10.1111/bjd.15600.

    Article  PubMed  CAS  Google Scholar 

  171. Han JS, Won CH, Chang SE, Lee MW, Choi JH, Moon KC. Primary cutaneous balloon cell melanoma: a very rare variant. Int J Dermatol. 2014;53(11):e535–6. https://doi.org/10.1111/ijd.12474.

    Article  PubMed  Google Scholar 

  172. Lawaetz M, Birch-Johansen F, Friis S, Eriksen JG, Kiss K, Gade S, Moller-Madsen M, Pourbordbari N, von Buchwald C. Primary mucosal melanoma of the head and neck in Denmark, 1982–2012: demographic and clinical aspects. A retrospective DAHANCA study. Acta Oncol. 2016;55(8):1001–8. https://doi.org/10.3109/0284186X.2016.1143117.

    Article  PubMed  Google Scholar 

  173. Mitteldorf C, Kempf W. Cutaneous pseudolymphoma. Surg Pathol Clin. 2017;10(2):455–76. https://doi.org/10.1016/j.path.2017.01.002.

    Article  PubMed  Google Scholar 

  174. Moreno-Ramirez D, Garcia-Escudero A, Rios-Martin JJ, Herrera-Saval A, Camacho F. Cutaneous pseudolymphoma in association with molluscum contagiosum in an elderly patient. J Cutan Pathol. 2003;30(7):473–5.

    Article  CAS  PubMed  Google Scholar 

  175. Terada T. Cutaneous pseudolymphoma: a case report with an immunohistochemical study. Int J Clin Exp Pathol. 2013;6(5):966–72.

    PubMed  PubMed Central  Google Scholar 

  176. Kim IS, Kim BR, Youn SW. Differentiation of Jessner’s lymphocytic infiltration of the skin from various chronic cutaneous lupus erythematosus subtypes by quantitative computer-aided image analysis. Dermatology. 2016;232(1):57–63. https://doi.org/10.1159/000440648.

    Article  PubMed  CAS  Google Scholar 

  177. Krieger BL. Lymphocytic infiltration of the skin (Jessner). Arch Dermatol. 1969;100(2):247–8.

    Article  CAS  PubMed  Google Scholar 

  178. Ziemer M, Eisendle K, Muller H, Zelger B. Lymphocytic infiltration of the skin (Jessner-Kanof) but not reticular erythematous mucinosis occasionally represents clinical manifestations of Borrelia-associated pseudolymphoma. Br J Dermatol. 2009;161(3):583–90. https://doi.org/10.1111/j.1365-2133.2009.09279.x.

    Article  PubMed  CAS  Google Scholar 

  179. Nakada T, Sueki H, Iijima M. Disseminated pagetoid reticulosis (Ketron-Goodman disease): six-year follow-up. J Am Acad Dermatol. 2002;47(2 Suppl):S183–6.

    Article  PubMed  Google Scholar 

  180. Steffen C. Ketron-Goodman disease, Woringer-Kolopp disease, and pagetoid reticulosis. Am J Dermatopathol. 2005;27(1):68–85.

    Article  PubMed  Google Scholar 

  181. Ahn CS, AL A, Sangueza OP. Mycosis fungoides: an updated review of clinicopathologic variants. Am J Dermatopathol. 2014;36(12):933–948; quiz 949–51. https://doi.org/10.1097/DAD.0000000000000207.

    Article  PubMed  Google Scholar 

  182. Hwang ST, Janik JE, Jaffe ES, Wilson WH. Mycosis fungoides and Sezary syndrome. Lancet. 2008;371(9616):945–57. https://doi.org/10.1016/S0140-6736(08)60420-1.

    Article  PubMed  CAS  Google Scholar 

  183. Lehman JS, Cook-Norris RH, Weed BR, Weenig RH, Gibson LE, Weaver AL, Pittelkow MR. Folliculotropic mycosis fungoides: single-center study and systematic review. Arch Dermatol. 2010;146(6):607–13. https://doi.org/10.1001/archdermatol.2010.101.

    Article  PubMed  Google Scholar 

  184. Martinez-Escala ME, Gonzalez BR, Guitart J. Mycosis fungoides variants. Surg Pathol Clin. 2014;7(2):169–89. https://doi.org/10.1016/j.path.2014.02.003.

    Article  PubMed  Google Scholar 

  185. Munoz-Gonzalez H, Molina-Ruiz AM, Requena L. Clinicopathologic variants of mycosis fungoides. Actas Dermosifiliogr. 2017;108(3):192–208. https://doi.org/10.1016/j.ad.2016.08.009.

    Article  PubMed  CAS  Google Scholar 

  186. Reddy K, Bhawan J. Histologic mimickers of mycosis fungoides: a review. J Cutan Pathol. 2007;34(7):519–25. https://doi.org/10.1111/j.1600-0560.2006.00662.x.

    Article  PubMed  Google Scholar 

  187. Chan BC, Stefanato CM, Moonim MT, Morris SL, Fields P, Dasgupta D, Therianou A, Whittaker SJ. Diffuse large B-cell lymphoma developing in erythrodermic cutaneous T-cell lymphoma: a case series. Br J Dermatol. 2017. https://doi.org/10.1111/bjd.15460.

  188. Russell-Jones R. Diagnosing erythrodermic cutaneous T-cell lymphoma. Br J Dermatol. 2005;153(1):1–5. https://doi.org/10.1111/j.1365-2133.2005.06706.x.

    Article  PubMed  Google Scholar 

  189. Vandersee S, Humme D, Terhorst D, Almohamad A, Mobs M, Beyer M. Evaluation of blood parameters for the monitoring of erythrodermic cutaneous T-cell lymphoma. J Dtsch Dermatol Ges. 2015;13(1):30–6. https://doi.org/10.1111/ddg.12549.

    Article  PubMed  Google Scholar 

  190. Ohtsuka M, Miura T, Yamamoto T. Clinical characteristics, differential diagnosis, and treatment outcome of subcutaneous panniculitis-like T-cell lymphoma: a literature review of published Japanese cases. Eur J Dermatol. 2017;27(1):34–41. https://doi.org/10.1684/ejd.2016.2914.

    Article  PubMed  Google Scholar 

  191. Yim JH, Kim MY, Kim HO, Cho B, Chung NG, Park YM. Subcutaneous panniculitis-like T-cell lymphoma in a 26-month-old child with a review of the literature. Pediatr Dermatol. 2006;23(6):537–40. https://doi.org/10.1111/j.1525-1470.2006.00305.x.

    Article  PubMed  Google Scholar 

  192. Quintanilla-Martinez L, Ridaura C, Nagl F, Saez-de-Ocariz M, Duran-McKinster C, Ruiz-Maldonado R, Alderete G, Grube P, Lome-Maldonado C, Bonzheim I, Fend F. Hydroa vacciniforme-like lymphoma: a chronic EBV+ lymphoproliferative disorder with risk to develop a systemic lymphoma. Blood. 2013;122(18):3101–10. https://doi.org/10.1182/blood-2013-05-502203.

    Article  PubMed  CAS  Google Scholar 

  193. Zhang X, Wang T, Wang L. Hydroa vacciniforme-like lymphoma in tibetan children: 2 cases and a literature review. Am J Dermatopathol. 2017. https://doi.org/10.1097/DAD.0000000000000880.

  194. Choi YL, Park JH, Namkung JH, Lee JH, Yang JM, Lee ES, Lee DY, Jang KT, Ko YH. Extranodal NK/T-cell lymphoma with cutaneous involvement: ‘nasal’ vs. ‘nasal-type’ subgroups--a retrospective study of 18 patients. Br J Dermatol. 2009;160(2):333–7. https://doi.org/10.1111/j.1365-2133.2008.08922.x.

    Article  PubMed  Google Scholar 

  195. Kim HJ, Kim SH, Oh SH. CD56-negative extranodal NK/T-cell lymphoma, nasal type, with extranasal cutaneous involvement. Ann Dermatol. 2015;27(5):618–20. https://doi.org/10.5021/ad.2015.27.5.618.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  196. Yu WW, Hsieh PP, Chuang SS. Cutaneous EBV-positive gammadelta T-cell lymphoma vs. extranodal NK/T-cell lymphoma: a case report and literature review. J Cutan Pathol. 2013;40(3):310–6. https://doi.org/10.1111/cup.12066.

    Article  PubMed  Google Scholar 

  197. Bogle MA, Riddle CC, Triana EM, Jones D, Duvic M. Primary cutaneous B-cell lymphoma. J Am Acad Dermatol. 2005;53(3):479–84. https://doi.org/10.1016/j.jaad.2005.04.043.

    Article  PubMed  Google Scholar 

  198. Sanusi T, Sun L, Wang C, Zhao Y, Huang C. Primary cutaneous diffuse large B-cell lymphoma of the face. J Dtsch Dermatol Ges. 2016;14(4):423–6. https://doi.org/10.1111/ddg.12815.

    Article  PubMed  Google Scholar 

  199. Barnes M, Van L, DeLong L, Lawley LP. Severity of cutaneous findings predict the presence of systemic symptoms in pediatric maculopapular cutaneous mastocytosis. Pediatr Dermatol. 2014;31(3):271–5. https://doi.org/10.1111/pde.12291.

    Article  PubMed  Google Scholar 

  200. Lange M, Niedoszytko M, Nedoszytko B, Lata J, Trzeciak M, Biernat W. Diffuse cutaneous mastocytosis: analysis of 10 cases and a brief review of the literature. J Eur Acad Dermatol Venereol. 2012;26(12):1565–71. https://doi.org/10.1111/j.1468-3083.2011.04350.x.

    Article  PubMed  CAS  Google Scholar 

  201. Neri I, Virdi A, Balestri R, Patrizi A. Diffuse cutaneous mastocytosis: a heterogeneous disease. Arch Dis Child. 2013;98(8):607. https://doi.org/10.1136/archdischild-2013-303839.

    Article  PubMed  Google Scholar 

  202. Bourji L, Kurban M, Abbas O. Solitary mastocytoma mimicking granuloma faciale. Int J Dermatol. 2014;53(12):e587–8. https://doi.org/10.1111/ijd.12577.

    Article  PubMed  Google Scholar 

  203. Hannaford R, Rogers M. Presentation of cutaneous mastocytosis in 173 children. Australas J Dermatol. 2001;42(1):15–21.

    Article  CAS  PubMed  Google Scholar 

  204. Lee HP, Yoon DH, Kim CW, Kim TY. Solitary mastocytoma on the palm. Pediatr Dermatol. 1998;15(5):386–7.

    Article  CAS  PubMed  Google Scholar 

  205. Comfere NI, Gonzalez Santiago TM, Peters MS, Knudson RA, Ketterling RP, Gibson LE. Cutaneous extramedullary plasmacytoma: clinical, prognostic, and interphase cytogenetic analysis. Am J Dermatopathol. 2013;35(3):357–63. https://doi.org/10.1097/DAD.0b013e31826d729f.

    Article  PubMed  Google Scholar 

  206. Tsang DS, Le LW, Kukreti V, Sun A. Treatment and outcomes for primary cutaneous extramedullary plasmacytoma: a case series. Curr Oncol. 2016;23(6):e630–46. https://doi.org/10.3747/co.23.3288.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  207. Wuu A, Bangert SD, Weber DM, Hymes SR. Primary cutaneous plasmacytoma. Cutis. 2014;93(6):E19–21.

    PubMed  Google Scholar 

  208. Gerds AT, Dao KH. Polycythemia vera management and challenges in the community health setting. Oncology. 2017;92(4):179–89. https://doi.org/10.1159/000454953.

    Article  PubMed  CAS  Google Scholar 

  209. Ongenae K, Janssens A, Noens L, Wieme N, Geerts ML, Beele H, Naeyaert JM. Erythromelalgia: a clue to the diagnosis of polycythemia vera. Dermatology. 1996;192(4):408–10.

    Article  CAS  PubMed  Google Scholar 

  210. Babina T, Miller L, Thomas B. Leukemia cutis. J Drugs Dermatol. 2012;11(3):416–7.

    PubMed  Google Scholar 

  211. Cruz Manzano M, Ramirez Garcia L, Sanchez Pont JE, Velazquez Manana AI, Sanchez JL. Rosacea-like leukemia cutis: a case report. Am J Dermatopathol. 2016;38(8):e119–21. https://doi.org/10.1097/DAD.0000000000000538.

    Article  PubMed  Google Scholar 

  212. Ratnam KV, Khor CJ, Su WP. Leukemia cutis. Dermatol Clin. 1994;12(2):419–31.

    Article  CAS  PubMed  Google Scholar 

  213. Marcoval J, Penin RM, Llatjos R, Martinez-Ballarin I. Cutaneous metastasis from lung cancer: retrospective analysis of 30 patients. Australas J Dermatol. 2012;53(4):288–90. https://doi.org/10.1111/j.1440-0960.2011.00828.x.

    Article  PubMed  Google Scholar 

  214. Junqueira AL, Corbett AM, Oliveira Filho J, Nasser Kda R, Haddad NN, Tebet AC. Cutaneous metastasis from gastrointestinal adenocarcinoma of unknown primary origin. An Bras Dermatol. 2015;90(4):564–6. https://doi.org/10.1590/abd1806-4841.20153175.

    Article  PubMed  PubMed Central  Google Scholar 

  215. Triantafyllou S, Georgia D, Gavriella-Zoi V, Dimitrios M, Stulianos K, Theodoros L, Georgios Z, Dimitrios T. Cutaneous metastases from esophageal adenocarcinoma. Int Surg. 2015;100(3):558–61. https://doi.org/10.9738/INTSURG-D-13-00257.1.

    Article  PubMed  PubMed Central  Google Scholar 

  216. Inadomi T. Sister Mary Joseph’s nodule: a clue to finding pancreatic cancer in a patient previously affected by gastric cancer. Eur J Dermatol. 2005;15(6):492–4.

    PubMed  Google Scholar 

  217. Pereira WA, Humaire CR, Silva CS, Fernandes LH. Sister Mary Joseph’s nodule: a sign of internal malignancy. An Bras Dermatol. 2011;86(4 Suppl 1):S118–20.

    Article  PubMed  Google Scholar 

  218. Renner R, Sticherling M. Sister Mary Joseph’s nodule as a metastasis of gallbladder carcinoma. Int J Dermatol. 2007;46(5):505–7. https://doi.org/10.1111/j.1365-4632.2006.03046.x.

    Article  PubMed  Google Scholar 

  219. Harvey G, Cochrane T. Carcinoma en cuirasse; primary lesion in stomach. AMA Arch Derm Syphilol. 1950;62(5):651–4.

    Article  CAS  PubMed  Google Scholar 

  220. Mullinax K, Cohen JB. Carcinoma en cuirasse presenting as keloids of the chest. Dermatol Surg. 2004;30(2 Pt 1):226–8.

    PubMed  Google Scholar 

  221. Xu P, Tan C. Primary breast carcinoma en cuirasse. J Dtsch Dermatol Ges. 2016;14(6):614–6. https://doi.org/10.1111/ddg.12877.

    Article  PubMed  Google Scholar 

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Zhu, YH. et al. (2018). Tumors of the Skin. In: Zhu, WY., Tan, C., Zhang, Rz. (eds) Atlas of Skin Disorders. Springer, Singapore. https://doi.org/10.1007/978-981-10-8037-1_27

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