onycholemmal carcinoma is believed to be of trichilemmal origin, and shows differentiation similar to that found in the trichilemmal portion of the hair follicle. less then 3 cases are currently in the english literature. all reported cases presented in elderly patients and were without recurrence after amputation. clinical presentation has been varied and can be very subtle. as with most nail tumors, pain is not a common feature. the diagnosis is based on the histology showing an infiltrative growth of atypical keratinocytes, one or more foci of abrupt keratinization, and usually also keratinous cysts devoid of a granular layer. when a cystic component and clear cells predominate, the subtype description of malignant proliferating onycholemmal cyst has been applied. no standard treatment option or follow up has been established.

Respuesta :

Rarely, "malignant proliferating onycholemmal cyst" and "onycholemmal carcinoma (OC)" have been used to characterize subungual malignant epithelial tumors with tricholemmal keratinization.

In addition to a nail bed carcinoma with tricholemmal microcysts, we also present a case of a slow-growing OC that developed on the middle finger of a 58-year-old male. This case was remarkable because it had sebaceous-apocrine differentiation.

Therefore, we believe that OC is a less appropriate name to describe this condition than microcystic nail bed cancer.

None of the uncommon cases of OC are known to match the additional traditional criteria for tricholemmal carcinoma provided by Headington, namely lobular organization, peripheral palisading, thicker basement membrane, and glycogen-positive tumor cells.

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