Syringocystadenocarcinoma papilliferum with coexisting trichoblastoma: A case report with review of literature

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Syringocystadenocarcinoma 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...

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Syringocystadenocarcinoma papilliferum: a rare tumor with a favorable prognosis.

Syringocystadenocarcinoma papilliferum (SCACP) is a rare adenexal carcinoma with only 21 cases reported in the literature. Most patients describe a long-standing mass with recent change, supporting the idea that SCACP arises from malignant transformation of pre-existing syringocystadenoma papilliferum (SCAP). Syringocystadenocarcinoma papilliferum is generally treated with wide surgical excisio...

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A case series of three atypical cases of syringocystadenoma papilliferum with thigh, abdomen and axillary involvement, and review of literature

Syringocystadenoma papilliferum is an uncommon benign apocrine gland tumour, mostly of congenital or early childhood onset, affecting head and neck. In addition, nevus sebaceous is commonly associated with this tumor. Here, we document three cases of syringocystadenoma papilliferum with many atypical features, such as the involvement of rare sites (abdomen, axilla and thigh), absence of nevus s...

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Chemoradiotherapy in a Case of Malignant Syringocystadenocarcinoma Papilliferum of Vulva with Locoregional Failure.

Introduction. Syringocystadenocarcinoma papilliferum (SCACP) is an extremely rare malignant adnexal tumor, which arises from syringocystadenoma papilliferum. To date, less than 30 cases of malignant SCACP have been reported, of which locoregional metastases were found in only four cases. Case Report. A 57-year-old female patient who presented to our Oncology Department with a recurrent malignan...

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Dentigerous Cyst Associated with a Deciduous Tooth: Report of a Case and Review of the Literature

Introdouction: Dentigerous cyst is a benign developmental lesion of the jaw. It is most commonly occurs during the second and third decades of life and has rarely been reported in association with a deciduous tooth. We report a case of two-year old girl who presented with an unerupted central incisor. According to the radiographic findings, she was diagnosed with a dentigerous cyst and...

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ژورنال

عنوان ژورنال: Indian Journal of Dermatology, Venereology and Leprology

سال: 2017

ISSN: 0378-6323

DOI: 10.4103/ijdvl.ijdvl_755_16