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POEMS综合征所致难治性腹水

Refractory ascites due to POEMS syndrome.

作者信息

Loeb J M, Hauger P H, Carney J D, Cooper A D

机构信息

Eden Hospital Medical Center, Castro Valley, Palo Alto Medical Foundation, California.

出版信息

Gastroenterology. 1989 Jan;96(1):247-9. doi: 10.1016/0016-5085(89)90789-0.

Abstract

A 52-yr-old woman developed exudative ascites 2 yr after the onset of peripheral neuropathy. Extensive evaluation revealed that the patient had no underlying liver disease, malignancy, infection, or cardiac or renal disease. The ascites initially responded to high-dose corticosteroid therapy. The patient had many clinical features of the recently described POEMS syndrome, including a persistent IgA lambda-paraprotein. Initially, her ascites responded to treatment with steroids. This is characteristic of the syndrome and should be considered in patients with POEMS syndrome and refractory ascites.

摘要

一名52岁女性在周围神经病变发作2年后出现渗出性腹水。全面评估显示,该患者没有潜在的肝脏疾病、恶性肿瘤、感染或心脏或肾脏疾病。腹水最初对高剂量皮质类固醇治疗有反应。该患者具有最近描述的POEMS综合征的许多临床特征,包括持续性IgA λ副蛋白。最初,她的腹水对类固醇治疗有反应。这是该综合征的特征,对于患有POEMS综合征和难治性腹水的患者应予以考虑。

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