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[获得性大疱性表皮松解症。一项临床病理研究]

[Acquired epidermolysis bullosa. A clinico-pathologic study].

作者信息

Rappersberger K, Konrad K, Schenk P, Tappeiner G

机构信息

I. Universitäts-Hautklinik Wien.

出版信息

Hautarzt. 1988 Jun;39(6):355-62.

PMID:3042704
Abstract

Epidermolysis bullosa acquisita is an immunologically mediated mechano-bullous dermatosis presenting with a variety of clinical appearances. In mild cases the skin lesions, serous blisters, erosions and scars are restricted to the extremities. Scarring alopecia, dystrophy and even loss of nails as well as extensive erosions of mucous membranes may complicate severe cases. The characteristic histopathological feature is a subepidermal blister, which is located within the dermis by electron microscopy. Linear deposits of IgG and C3 along the basement membrane zone have been found on the dermal side of the lamina densa by immunoelectron microscopy. This close anatomical relationship with anchoring fibrils strongly suggests a functional disturbance of these anatomical structures, leading to dermolytic blistering. Treatment with sulphones, in combination with cortico-steroids in the more severe cases, has resulted in long-term improvement in two of our three patients.

摘要

获得性大疱性表皮松解症是一种免疫介导的机械性大疱性皮肤病,具有多种临床表现。轻症患者的皮肤损害、浆液性水疱、糜烂和瘢痕局限于四肢。重症患者可能并发瘢痕性脱发、甲营养不良甚至甲缺失,以及广泛的黏膜糜烂。其特征性组织病理学表现为表皮下水疱,电镜下位于真皮内。免疫电镜检查发现,在致密板的真皮侧有IgG和C3沿基底膜带呈线性沉积。这种与锚原纤维紧密的解剖学关系强烈提示这些解剖结构存在功能障碍,导致皮肤松解性水疱形成。在病情较重的病例中,使用砜类药物联合皮质类固醇进行治疗,使我们三名患者中的两名获得了长期改善。

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