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Concurrence of Acrodermatitis Enteropathica and Eczema Herpeticum in a Child with Atopic Dermatitis

机译:小儿特应性皮炎的合并小肠皮炎和小疱疹湿疹

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摘要

Acrodermatitis enteropathica (AcE) is a rare, autosomal recessive inherited disorder caused by mutation of the SLC39A4 gene coding for zinc transport protein (ZIP 4). The disease appears during childhood especially in breastfeeding or post-breastfeeding infant. Eczema herpeticum refers to a disseminated skin infection of herpes simplex virus that usually leads to vesicular eruptions commonly seen on a background of atopic dermatitis (AD). We describe an 11-year-old boy with periorificial erosions in periorbital, perinasal, perioral, perineal, and gluteal areas, accompanied with itchy vesicles, some covered with hemorrhagic crusts. A clinical diagnosis of AcE and eczema herpeticum with AD was supported by typical lesions and acute and chronic eczematous changes found mainly in the flexural aspects of extremities, which is diagnostic of AD. Laboratory findings showed anti HSV1 IgG (23.43) and high levels of IgE (478.9 IU/L). There was no multinucleated giant cell in the Tzanck test. Skin histology was compatible with AcE. Direct immunofluorescent examination showed no deposits of IgG, IgM, IgA, or complement. Complete resolution occurred within 2 weeks of acyclovir and oral zinc supplementation.
机译:肠炎性皮炎(AcE)是一种罕见的常染色体隐性遗传性疾病,由编码锌转运蛋白(ZIP 4)的SLC39A4基因突变引起。该病在儿童时期尤其是在母乳喂养或母乳喂养后的婴儿中出现。疱疹湿疹是指单纯性疱疹病毒的弥漫性皮肤感染,通常会导致异位性皮炎(AD)背景上的水疱爆发。我们描述了一个11岁的男孩,在眶周,鼻周,口周,会阴和臀肌区有骨周糜烂,并伴有发痒的囊泡,有些囊肿覆盖有出血性硬皮。典型的病变以及主要在四肢的弯曲方面发现的急,慢性湿疹改变均支持AD的AcE和疱疹性湿疹的临床诊断,这是AD的诊断。实验室检查结果显示抗HSV1 IgG(23.43)和高水平的IgE(478.9 IU / L)。 Tzanck试验中没有多核巨细胞。皮肤组织学与AcE相容。直接免疫荧光检查显示没有IgG,IgM,IgA或补体沉积。阿昔洛韦和口服锌补充剂的2周内完全消退。

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