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小儿菊池病的腋窝受累情况。

Axillary involvement in pediatric Kikuchi's disease.

作者信息

Heldenberg D, Amar M, Ben-Arie Y, Iuchtman M

机构信息

Department of Pediatrics, Hillel Yaffe Medical Center, Hadera, Israel.

出版信息

Eur J Pediatr Surg. 1996 Feb;6(1):32-4. doi: 10.1055/s-2008-1066464.

Abstract

We report the first Israeli pediatric case of Kikuchi's disease in a 10-year-old male. He was hospitalized for evaluation of migrating arthralgia and fever. Axillary adenopathy was the main physical finding. A biopsy showed a histiocytic necrotizing lymphadenitis. Diagnosis, therapeutic options and the clinical significance of Kikuchi's disease are discussed. Kikuchi's disease should be considered in the differential diagnosis of fever of unknown origin in children, even in the absence of cervical adenopathy. A long follow-up is advised because of possible links with systemic lupus erythematosus and to detect eventual late recurrences.

摘要

我们报告了以色列首例10岁男性儿童的菊池病病例。他因游走性关节痛和发热入院评估。腋窝淋巴结肿大是主要的体格检查发现。活检显示为组织细胞性坏死性淋巴结炎。本文讨论了菊池病的诊断、治疗选择及临床意义。即使没有颈部淋巴结肿大,在儿童不明原因发热的鉴别诊断中也应考虑菊池病。鉴于其与系统性红斑狼疮可能存在关联并为检测最终的晚期复发,建议进行长期随访。

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