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[巨细胞病毒感染继发小儿梅内特里耶病:一家高复杂性中心的两例临床病例报告]

[Ménétrier's disease in pediatric patients secondary to cytomegalovirus infection: Presentation of two clinical cases in a high complexity center].

作者信息

Tagliaferro Gustavo, Llera Julián, Orsi Marina

机构信息

Hospital Italiano de Buenos Aires.

出版信息

Arch Argent Pediatr. 2019 Apr 1;117(2):e158-e162. doi: 10.5546/aap.2019.e158.

Abstract

Ménétrier's disease is a protein losing gastroenteropathy. Defined as a rare entity with an unknown cause, most of the reported cases have been associated with viral infections. In pediatric patients, it is characterized by an acute onset with a benign and self-limiting course. It is characterized by thickened gastric folds that generally involve the body and the gastric fundus, associated with hypoalbuminemia due to the loss of serum protein through the mucosa. The following are two clinical cases of infant Ménétrier syndrome associated with cytomegalovirus infection.

摘要

梅内特里耶病是一种蛋白丢失性胃肠病。它被定义为一种病因不明的罕见疾病,大多数报道的病例都与病毒感染有关。在儿科患者中,其特点是急性起病,病程良性且自限性。其特征为胃皱襞增厚,通常累及胃体和胃底,由于血清蛋白通过黏膜丢失而伴有低白蛋白血症。以下是两例与巨细胞病毒感染相关的婴儿梅内特里耶综合征的临床病例。

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