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系统性红斑狼疮患者的假性假性梅格斯综合征。

Pseudo-pseudo Meigs' syndrome in a patient with systemic lupus erythematosus.

机构信息

Division of Rheumatology, NYU Hospital for Joint Diseases, USA.

出版信息

Lupus. 2012 Nov;21(13):1463-6. doi: 10.1177/0961203312461291. Epub 2012 Sep 14.

Abstract

Pseudo-pseudo Meigs' syndrome (PPMS) is a rare manifestation of patients with systemic lupus erythematosus (SLE), defined by the presence of ascites, pleural effusions and an elevated CA-125 level. We describe a patient with longstanding lupus who presented with localized lymphadenopathy and subsequently developed massive chylous ascites with marked hypoalbuminemia. A brief historical overview of Meigs' syndrome and related entities is presented, along with a discussion of the differential diagnosis of hypoalbuminemia and ascites in an SLE patient. In addition, we speculate on the optimal therapeutic intervention in such a patient.

摘要

假性假性梅格斯综合征(PPMS)是系统性红斑狼疮(SLE)患者的一种罕见表现,其特征为腹水、胸腔积液和 CA-125 水平升高。我们描述了一位患有长期狼疮的患者,其最初表现为局部淋巴结病,随后出现大量乳糜性腹水伴显著低白蛋白血症。本文简要回顾了梅格斯综合征及相关疾病,并讨论了 SLE 患者低白蛋白血症和腹水的鉴别诊断。此外,我们还推测了此类患者的最佳治疗干预措施。

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