Pigmented Bowen disease

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چکیده

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منابع مشابه

[Clinical and dermoscopic features of pigmented Bowen disease].

could be discerned. Biopsy showed a tumor confined to the epidermis with acanthosis, a certain degree of papillomatosis, markedly atypical cells, and mitotic figures, with a completely intact basement membrane. Immunohistochemical studies using markers such as Melan-A and pancytokeratin cocktail confirmed the nature of the tumor, which was diagnosed as a case of pigmented Bowen disease. We exci...

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Multicentric Bowen disease in linear porokeratosis.

Linear porokeratosis is a genodermatosis, caused by a clonal proliferation of keratinocytes along the lines of Blaschko. This type of porokeratosis is particularly susceptible to malignant degeneration e.g. to Bowen disease, a squamous cell carcinoma (SCC) in situ with the potential for significant lateral spread. Here we report a case of linear porokeratosis on the left leg of a 56-year-old ma...

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Pagetoid Bowen Disease Initially Misdiagnosed as Ectopic Extramammary Paget's Disease

Pagetoid Bowen disease is a histological variant of Bowen disease which demonstrates large pale staining cells (pagetoid cells). It requires differential diagnosis from other cutaneous malignancies with similar patterns, such as extramammary Paget's disease (EMPD) and Pagetoid melanoma in situ. Herein, we report a case of Pagetoid Bowen disease which was initially misdiagnosed as ectopic EMPD.

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Pigmented Bowens disease mimicking malignant Melanoma: A case report

Pigmented Bowens disease is an in situ squamous cell carcinoma, which is seldom reported in white patients. Herein we report a 20-year-old woman with type III skin, who had this lesion on the fourth finger of her right hand, similar to superficial malignant melanoma, clinically. Although dermoscopic evaluation could be helpful, correct diagnosis of non-melanotic origin is done by histological e...

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Pigmented Nodular Adrenocortical Disease

Carney complex (CNC) is a multiple endocrine neoplasia (MEN) syndrome associated with other, non-endocrine manifestations such as lentigines, cardiac myxomas and schwannomas. Primary pigmented nodular adrenocortical disease (PPNAD), leading to corticotrophin-independent Cushing’s syndrome is the most frequent endocrine lesion in CNC. The complex has been mapped to 2p16 and 17q22-24, although ad...

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ژورنال

عنوان ژورنال: Canadian Medical Association Journal

سال: 2017

ISSN: 0820-3946,1488-2329

DOI: 10.1503/cmaj.170810