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儿童慢性大疱性皮肤病(线状IgA大疱性皮病)的罕见临床病理及免疫学表现

Unusual clinicopathological and immunological presentation of chronic bullous dermatosis of childhood (linear IgA dermatosis).

作者信息

Fahad Al-Saif, Ammar Al-Rikabi

机构信息

Department of Dermatology, King Khalid University Hospital and King Saud University, Riyadh, Kingdom of Saudi Arabia.

出版信息

Indian J Dermatol. 2011 Sep-Oct;56(5):573-5. doi: 10.4103/0019-5154.87159.

Abstract

Linear IgA bullous dermatosis is a rare sulfone-responsive subepidermal blistering disorder of unknown etiology in which smooth linear deposits of IgA are found in the basement membrane zone. Chronic bullous dermatosis of childhood is equivalent to linear IgA disease of adulthood and is characterized by an abrupt onset of large, widespread and tense bullae on a normal or erythematous base. In this case, we describe an unusual presentation of chronic bullous dermatosis in a 14-month-old Saudi girl. Histopathological examination revealed subepidermal cell poor blisters with linear deposition of IgA, IgG, IgM, and C3 along the dermoepidermal junction. The unusual clinical, histopathological and immunofluorescence findings in this patient are discussed, with an account on the differential diagnosis in such cases along with a detailed review of the relevant literature.

摘要

线状IgA大疱性皮肤病是一种罕见的、对砜类药物有反应的表皮下大疱性疾病,病因不明,在基底膜带可见IgA的光滑线状沉积。儿童慢性大疱性皮肤病等同于成人线状IgA病,其特征为在正常或红斑基底上突然出现大的、广泛且紧张的水疱。在此病例中,我们描述了一名14个月大的沙特女孩慢性大疱性皮肤病的不寻常表现。组织病理学检查显示表皮下细胞少的水疱,IgA、IgG、IgM和C3沿真皮表皮交界处呈线状沉积。本文讨论了该患者不寻常的临床、组织病理学和免疫荧光表现,并阐述了此类病例的鉴别诊断以及对相关文献的详细综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a18/3221227/e39bc9e61d3a/IJD-56-573-g001.jpg

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