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免疫功能正常的成年人巨细胞病毒相关蛋白丢失性胃病:一例报告

Cytomegalovirus-associated protein losing gastropathy in an immunocompetent adult: a case report.

作者信息

Setakhr Vida, Muller Gebhard, Hoang Pierre, Lambert Anne Sophie, Geubel André

机构信息

Department of Gastroenterology, Sainte Elisabeth Hospital, Namur, Belgium.

出版信息

Acta Gastroenterol Belg. 2007 Jul-Sep;70(3):296-9.

Abstract

Cytomegalovirus infection of the gastro-intestinal tract is frequent and may be serious in the immunocompromised patient. We report a case of cytomegalovirus infection in an immunocompetent young man who presented total food intolerance, pleural effusion and oedema as the result of severe protein losing hypertrophic gastropathy. Hypertrophic gastropathy with severe mucosal protein loss has been described in Menetrier's disease, a condition of unknown cause which involves foveolar hyperplasia of the gastric mucosa. Related hypoalbuminemia is responsible for a clinical picture of diffuse edema. In adults, the natural course of the disease is marked by a chronic course and carries a bad prognosis. In our case, the disease ran a protracted disabling course, likely shortened by ganciclovir therapy, followed by slow clinical, endoscopic and biochemical resolution after several' months course.

摘要

胃肠道巨细胞病毒感染很常见,在免疫功能低下的患者中可能很严重。我们报告一例免疫功能正常的年轻男性巨细胞病毒感染病例,该患者因严重的蛋白丢失性肥厚性胃炎出现完全食物不耐受、胸腔积液和水肿。肥厚性胃炎伴严重黏膜蛋白丢失已在梅内特里耶病中有所描述,该病病因不明,涉及胃黏膜小凹增生。相关的低蛋白血症导致弥漫性水肿的临床表现。在成年人中,该病的自然病程以慢性病程为特征,预后不良。在我们的病例中,疾病呈迁延性致残病程,可能因更昔洛韦治疗而缩短,经过数月病程后临床、内镜及生化指标缓慢恢复。

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