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A Case of Malignant Eccrine Poroma Developing on Suprapubic Area

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초록

Malignant eccrine poroma is a rare skin appendageal tumor arising from the intraepidermal ductal portion of the eccrine sweat gland. It may develop either spontaneously or from a long-standing eccrine poroma. It usually affects the aged and is located most commonly on lower extremities. We report a case of malignant eccrine poroma occurring on the suprapubic area of a 75-year-old Korean man. He underwent wide excision and flap coverage.

Abstract

Malignant eccrine poroma is a rare skin appendageal tumor arising from the intraepidermal ductal portion of the eccrine sweat gland. It may develop either spontaneously or from a long-standing eccrine poroma. It usually affects the aged and is located most commonly on lower extremities. We report a case of malignant eccrine poroma occurring on the suprapubic area of a 75-year-old Korean man. He underwent wide excision and flap coverage.

참고문헌 (10)

  1. Pinkus H, "Epidermotropic eccrine carcinoma; a case combining features of eccrine poroma and Paget's dermatosis", Arch Dermatol, 88, pp.597~606 (1963)
  2. Mishima Y, "Oncogenic differentiation of the intraepidermal eccrine sweat duct: eccrine poroma, poroepithelioma, and porocarcinoma", Der-matologica, 138, pp.238~250 (1969)
  3. Kim JS, "A case of malignant eccrine poroma", Korean J Dermatol, 36, pp.717~721 (1998)
  4. Jung DY, "A case of malignant eccrine poroma", Korean J Dermatol, 37, pp.660~664 (1999)
  5. Han KS, "A case of malignant eccrine poroma", Korean J Dermatol, 39, pp.247~250 (2001)
  6. Kim YJ, "A case of malignant eccrine poroma", Korean J Dermatol, 40, pp.442~444 (2002)
  7. Snow SN, "Eccrine porocarcinoma of the face", J Am Acad Dermatol, 27, pp.306~311 (1992)
  8. Sung KJ, "Immunohistochemical study of eccrine tumors", Korean J Dermatol, 30, pp.303~315 (1992)
  9. Shaw M, "Malignant eccrine poroma: a study of twenty-seven cases", Br J Dermatol, 107, pp.675~680 (1982)
  10. Mehregan CAH, "Eccrine adenocarcinoma: a clinicopathologic study of 35 cases", Arch Dermatol, 119, pp.104~114 (1983)

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