原发性Sjögren综合征患者的Bowen病:1例报告和文献回顾

IF 0.2 Q4 DERMATOLOGY
Besma Ben Dhaou, Imen Rachdi, Rym Ben Mously, Zohra Aydi, Fatma Daoud, Lilia Baili, Insaf Mokhtar, Fatma Boussema
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引用次数: 1

摘要

本文报道一例罕见的鲍恩氏病(BD)患者原发性Sjögren综合征。一名患有原发性Sjögren综合征的42岁妇女,根据临床和血清学发现,3年后因生殖器出血入院。Bowen病的诊断是通过临床和组织病理学检查确定的。本文描述了淋巴瘤与Sjögren’s综合征的经典关联,但据我们所知,这是已发表文献中关于BD与Sjögren’s综合征关联的第二篇报道。不能排除常见的生理病理病因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bowen’s disease in a patient with Primary Sjögren’s syndrome: A case report and a review of the literature

A rare case of Bowen’s disease (BD) in a patient with Primary Sjögren’s syndrome is reported. A 42-year-old woman suffering from Primary Sjögren’s syndrome retained on the basis of clinical and serological findings, was admitted 3 years later for genital bleeding. The diagnosis of Bowen’s disease was established by clinical and histolopathological examination. Classical association of lymphoma and Sjögren’s syndrome is described, but to the best of our knowledge, it is the second report of BD associated to Sjögren’s syndrome in published literature. A common physio-pathological etiology cannot be excluded.

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