成人遗传性大疱性表皮松解症伴交界性水疱形成
Epidermolysis bullosa hereditaria with junctional blistering in an adult.
作者信息
Hashimoto I, Schnyder U W, Anton-Lamprecht I
出版信息
Dermatologica. 1976;152(2):72-86. doi: 10.1159/000251166.
PMID:939338
Abstract
A 38-year-old patient with epidermolysis bullosa is described, in whom junctional blister formation is revealed by electron microscopy. Clinical and ultrastructural differences from the recessive dystrophic type (Hallopeau-Siemens) and from the lethal type (Herlitz) of epidermolysis bullosa are discussed in detail.
摘要
本文描述了一名38岁的大疱性表皮松解症患者，其通过电子显微镜检查发现有交界性水疱形成。文中详细讨论了该病例与隐性营养不良型（Hallopeau-Siemens型）和致死型（Herlitz型）大疱性表皮松解症在临床和超微结构上的差异。
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