Suppr超能文献

具有硬斑病样临床表现的常染色体隐性遗传性浆细胞性脂膜炎。

Autosomal recessive plasma cell panniculitis with morphea-like clinical manifestation.

作者信息

Hamadah Issam R, Banka Nusrat

机构信息

Department of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

出版信息

J Am Acad Dermatol. 2006 May;54(5 Suppl):S189-91. doi: 10.1016/j.jaad.2005.06.032.

Abstract

Two siblings had hyperpigmented indurations over the inner aspects of both thighs extending to the lower abdomen. Skin biopsy showed plasma cell panniculitis favoring a diagnosis of morphea profundus. Family history of consanguinity was present, but both parents were unaffected. To our knowledge this is the first report of autosomal recessive plasma cell panniculitis with the clinical manifestations of morphea.

摘要

两名兄弟姐妹双侧大腿内侧至下腹部出现色素沉着性硬结。皮肤活检显示浆细胞性脂膜炎,倾向于诊断为深部硬斑病。家族中有近亲结婚史,但父母均未患病。据我们所知,这是首例具有硬斑病临床表现的常染色体隐性浆细胞性脂膜炎报告。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验