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[伴有IgA沉积的单侧眼睑松弛症]

[Unilateral blepharochalasis with IgA-deposits].

作者信息

Schaeppi H, Emberger M, Wieland U, Metze D, Bauer J W, Pohla-Gubo G, Thaller-Antlanger H, Hintner H

机构信息

Landesklinik für Dermatologie, Landeskliniken Salzburg, Germany.

出版信息

Hautarzt. 2002 Sep;53(9):613-7. doi: 10.1007/s00105-001-0303-y.

Abstract

A 36-year-old male patient presented with unilateral periocular skin atrophy. The blepharochalasis developed without any obvious inflammation of the eyelids over the past 10 years. Interestingly, elongated blood vessels and microaneurysmatic vessel changes were found in the tarsal conjunctiva. A punch biopsy revealed a nearly complete loss of elastic fibres in the papillary and superficial reticular dermis. The contralateral side was histopathologically normal. On immunohistology IgA-deposits could be observed especially on perifollicular elastic fibres. Immunoelectronmicroscopy confirmed the diagnosis and suggested fibulin and fibronectin as potential binding sites for the autoantibodies. This further report of elastolysis in association with IgA-autoantibodies defines the autoantibody binding site in more detail and suggests that the immune mechanisms may also play a role in vessel changes of the conjunctiva.

摘要

一名36岁男性患者出现单侧眼周皮肤萎缩。睑皮肤松弛症在过去10年中逐渐发展,眼睑无明显炎症。有趣的是,在睑板结膜发现了延长的血管和微动脉瘤样血管改变。打孔活检显示乳头层和浅表网状真皮层的弹性纤维几乎完全缺失。对侧组织病理学正常。免疫组织化学检查发现IgA沉积,尤其是在毛囊周围弹性纤维上。免疫电子显微镜检查确诊并提示纤维蛋白和纤连蛋白可能是自身抗体的结合位点。这份关于弹性纤维溶解与IgA自身抗体相关的进一步报告更详细地确定了自身抗体结合位点,并提示免疫机制可能也在结膜血管改变中起作用。

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