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遗传性致死性大疱性表皮松解症:病理学、自然病史与治疗

Epidermolysis bullosa hereditaria letalis: pathology, natural history and therapy.

作者信息

Schachner L, Lazarus G S, Dembitzer H

出版信息

Br J Dermatol. 1977 Jan;96(1):51-8. doi: 10.1111/j.1365-2133.1977.tb05185.x.

Abstract

A patient with epidermolysis bullosa hereditaria letalis had the characteristic electron microscopic lesions not only in the skin, but also in the gastro-intestinal, genito-urinary and respiratory tracts. Administration of dexamethasone to this patients resulted in a significant decrease in the blistering. Although the patient died, long term survival in this disease is not rare. We report that staining tissue specimens from patients with epidermolysis bullosa with fluorescein-labelled bullous pemphigoid antibody is a reliable method for differentiating between junctional and dystrophic disease.

摘要

一名遗传性致死性大疱性表皮松解症患者不仅在皮肤,而且在胃肠道、泌尿生殖道和呼吸道都有特征性的电子显微镜下病变。给该患者使用地塞米松后水疱形成明显减少。尽管该患者死亡,但这种疾病的长期存活并不罕见。我们报告,用荧光素标记的大疱性类天疱疮抗体对大疱性表皮松解症患者的组织标本进行染色是区分交界性和营养不良性疾病的可靠方法。

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