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新生儿线状免疫球蛋白A大疱性皮肤病:一种罕见的表现。

Neonatal linear immunoglobulin a bullous dermatosis: a rare presentation.

作者信息

Julapalli Meena R, Brandon Kirra L, Rosales Cecilia M, Grover Raminder K, Plunkett Richard W, Metry Denise W

机构信息

Department of Dermatology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Pediatr Dermatol. 2012 Sep-Oct;29(5):610-3. doi: 10.1111/j.1525-1470.2011.01507.x. Epub 2011 Sep 9.

Abstract

Linear immunoglobulin A bullous dermatosis (LABD) is an autoimmune blistering disease that most commonly presents in preschool-aged children. There have been few neonatal reports, all of which had life-threatening aerodigestive complications requiring mechanical intervention and systemic therapy. We present a case of LABD in a neonate who had an uncomplicated course and was treated conservatively with only low-potency topical corticosteroids and wound care before resolution of his skin lesions.

摘要

线状免疫球蛋白A大疱性皮肤病(LABD)是一种自身免疫性大疱性疾病,最常见于学龄前儿童。新生儿病例报道较少,所有这些病例均有危及生命的气消化道并发症,需要机械干预和全身治疗。我们报告一例新生儿LABD病例,该患儿病程顺利,在皮肤病变消退前仅采用低效外用糖皮质激素和伤口护理进行保守治疗。

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