Syringocystadenocarcinoma Papilliferum In Situ–Like Changes in Extramammary Paget Disease: A Report of 11 Cases
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چکیده
منابع مشابه
Extramammary Paget disease: a report of 10 cases.
Extramammary Paget disease (EMPD) is a very rare form of intraepithelial adenocarcinoma. We report the cases of EMPD diagnosed in a referral hospital over a 5-year period from 2009 to 2013. Ten cases of EMPD were diagnosed in 4 men and 6 women aged between 50 and 79 years. Erroneous clinical diagnoses led to diagnostic delays of 1 to 5 years in all cases. Six patients had in situ lesions and de...
متن کاملSyringocystadenocarcinoma Papilliferum: A Case Report
Syringocystadenocarcinoma papilliferum (SCACP) is a rare form of adenocarcinoma of the skin. This is the malignant counterpart of syringocystadenoma papilliferum (SCAP) and usually develops on the scalp in a long-standing lesion identified clinically as SCAP. We describe a 65-yr-old Korean man with a nodule on the right supra-pubic area with a 2-yr duration. Histologically this tumor had a simi...
متن کاملExtramammary Paget Disease of the Vulva - Case Report.
Extramammary Paget disease (EPD) is a rare malign neoplasm that may affect the vulva and has manifestations common to benign diseases such as itching, pain and eczema. This leads to delay in diagnosis and consequent worse prognosis. The definitive diagnosis is obtained by biopsy of the vulva, which shows Paget cells. The treatment of choice is wide excision with margins, which leads to sequelae...
متن کامل[Extramammary paget disease: report of 2 cases treated by mohs micrographic surgery].
Actas Dermosifiliogr. 2009;100:235-48 239 To the Editor: Extramammary Paget disease (EPD), first described by Crocker1 in 1889, is a rare intraepithelial neoplasia of regions of the skin rich in apocrine glands. The lesions present clinically as erythematous scaly or slightly pruriginous plaques, and histological studies show cells with large cytoplasm and prominent nucleoli throughout the epid...
متن کاملSyringocystadenocarcinoma Papilliferum in the Perianal Area
Syringocystadenocarcinoma papilliferum (SCACP) is a very rare cutaneous adnexal neoplasm. SCACP presents histologic variability, and it is difficult to establish the diagnosis from a punch biopsy. SCACP has an overall configuration similar to that of syringocystadenoma papilliferum (SCAP). When we diagnose SCACP, the histologic features of SCAP can be contributing and immunohistochemical staini...
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ژورنال
عنوان ژورنال: The American Journal of Dermatopathology
سال: 2016
ISSN: 0193-1091
DOI: 10.1097/dad.0000000000000554