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线状IgA大疱性皮病:十例成年患者的研究

Linear IgA dermatosis: a study of ten adult patients.

作者信息

Mobacken H, Kastrup W, Ljunghall K, Löfberg H, Nilsson L A, Svensson A, Tjernlund U

出版信息

Acta Derm Venereol. 1983;63(2):123-8.

PMID:6189326
Abstract

Ten adult patients with homogeneous-linear deposition of IgA along the basement membrane zone have been studied. The direct immunofluorescence IgA pattern was stable, and there was no deposition of IgG or IgM. The clinical presentations were heterogeneous and resembled dermatitis herpetiformis (DH) (3 cases) or bullous pemphigoid (5 cases). Two patients had widespread gyrate blistering lesions of acute onset. Pruritus was constantly present. The course of the disease was chronic except for one patient who had a spontaneous remission after 5 years. The histology was indistinguishable from "classical" DH with granular IgA in dermal papillae. The patients studied in the present investigation did not show the high incidence of atrophic intestinal villi found in "classical" DH. Five of 9 cases carried the haplotype HLA-A1, B8, DR3. In spite of a close similarity between linear IgA dermatosis and DH, differences exist which indicate discrepancies in etiopathogenesis.

摘要

对10例沿基底膜带呈均质性线性IgA沉积的成年患者进行了研究。直接免疫荧光IgA模式稳定,未发现IgG或IgM沉积。临床表现各异,类似疱疹样皮炎(DH)(3例)或大疱性类天疱疮(5例)。2例患者有急性起病的广泛回旋状水疱性皮损。瘙痒持续存在。除1例患者在5年后自发缓解外,病程为慢性。组织学表现与真皮乳头中有颗粒状IgA的“经典”DH无法区分。本研究中的患者未显示出“经典”DH中发现的萎缩性肠绒毛的高发生率。9例中有5例携带单倍型HLA-A1、B8、DR3。尽管线性IgA皮肤病与DH非常相似,但仍存在差异,这表明在病因发病机制上存在差异。

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