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先天性头皮皮肤缺失与单纯疱疹病毒。病例报告。

Congenital absence of scalp skin and herpes simplex virus. A case report.

作者信息

Tomer A, Harel A

出版信息

Isr J Med Sci. 1983 Oct;19(10):950-1.

PMID:6662680
Abstract

A male infant, born at 40 weeks' gestation of a 27-year-old mother, presented at delivery with three scalp lesions, 2 to 4 cm in diam, covered with necrotic tissue and devoid of hair. The infant was born by natural vertex delivery within 2 hours of membrane rupture; birth weight was 3,300 g and Apgar score 10. There were no other skin lesions, and physical and neurological examinations were normal. Herpes simplex virus Type 2 was isolated from the lesions and the mother's cervix. High titers of IgG and IgM antibodies in the serum of mother and infant indicated an intrauterine infection. The skin ulcers healed within 1 month, with gradual epithelization and formation of a hairless atrophic scar.

摘要

一名男婴,孕40周出生,母亲27岁。出生时头皮有三处皮损,直径2至4厘米,覆盖坏死组织且无毛发。婴儿在胎膜破裂后2小时内自然头位分娩出生;出生体重3300克,阿氏评分10分。无其他皮肤损害,体格检查和神经检查均正常。从皮损处及母亲宫颈分离出单纯疱疹病毒2型。母婴血清中高滴度的IgG和IgM抗体表明存在宫内感染。皮肤溃疡在1个月内愈合,逐渐上皮化并形成无毛萎缩性瘢痕。

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