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[詹诺蒂-克罗西综合征。乙肝表面抗原阴性丘疹性肢端皮炎,一种婴儿丘疹水疱性肢端局限性综合征]

[Gianotti-Crosti syndrome. HBsAG-negative papular acrodermatitis, an infantile papulovesicular acrolocalized syndrome].

作者信息

Ehringhaus C, Happle R, Dominick H C, Brune K H

出版信息

Monatsschr Kinderheilkd. 1985 Feb;133(2):111-3.

PMID:2984558
Abstract

We report three cases of the Gianotti-Crosti syndrome (papulovesicular-acro-located syndrome of childhood), a self-limited common disease of childhood, which may be caused by various viral infections. The hepatitis B virus, however, is excluded by definition as a causal agent. The syndrome is characterized by itching papulo-vesicular skin lesions measuring 1-5 mm in diameter and localized to the limbs and face. The clinical and terminological differences between the HBsAG negative Gianotti-Crosti syndrome and the HBsAG positive Gianotti disease are emphasized.

摘要

我们报告了三例詹诺蒂-克罗sti综合征(儿童丘疹水疱性肢端综合征),这是一种儿童常见的自限性疾病,可能由多种病毒感染引起。然而,根据定义,乙肝病毒被排除为致病因素。该综合征的特征是直径为1 - 5毫米的瘙痒性丘疹水疱性皮肤损害,局限于四肢和面部。文中强调了HBsAG阴性的詹诺蒂-克罗sti综合征与HBsAG阳性的詹诺蒂病在临床和术语上的差异。

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