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儿童木村病合并肾病综合征——一种罕见的关联。

Kimura disease with nephrotic syndrome in a child- A rare association.

作者信息

Majumder Anusree, Sen Debraj

机构信息

Department of Pathology, Military Hospital Jodhpur, Jodhpur, Rajasthan, India.

Department of Radiodiagnosis and Imaging, Command Hospital, Pune, Maharashtra, India.

出版信息

Indian J Pathol Microbiol. 2019 Jul-Sep;62(3):437-440. doi: 10.4103/IJPM.IJPM_517_18.

Abstract

Lymphadenopathy along with various systemic manifestations is commonly encountered in pediatric patients, tuberculosis being the commonest etiology. Occasional patients may present a diagnostic conundrum. Here, the authors report an unusual manifestation of Kimura disease (KD) presenting as nephrotic syndrome associated with mesenteric lymphadenitis in an 11-year-old male child. KD is a chronic inflammatory disorder of unknown etiology. It typically affects young adult males in the age range of 27-40 years and usually presents as painless itchy nodular masses in the head and neck region. The involvement of mesenteric lymph nodes along with a very young age of presentation makes it a rare case, posing a diagnostic challenge for the unsuspecting physician.

摘要

小儿患者中常见伴有各种全身表现的淋巴结病,其中结核病是最常见的病因。偶尔会有患者带来诊断难题。在此,作者报告了1例不寻常的木村病(KD)表现,该例为11岁男性儿童,以肾病综合征合并肠系膜淋巴结炎形式出现。KD是一种病因不明的慢性炎症性疾病。它通常影响27至40岁的年轻成年男性,通常表现为头颈部无痛性瘙痒性结节肿块。肠系膜淋巴结受累且发病年龄很小,使其成为罕见病例,给毫无防备的医生带来诊断挑战。

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