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组织细胞坏死性淋巴结炎(菊池藤本病)——4例报告

Histiocytic necrotizing lymphadenitis (Kikuchi Fujimoto Disease)--a report of four cases.

作者信息

Basu Debdatta, Mutha Sucheeta M

机构信息

Department of Pathology, Jawahar Lal Instiute of Post Graduate Medical Education and Research, Pondicherry, India.

出版信息

Indian J Pathol Microbiol. 2002 Jan;45(1):89-91.

Abstract

Four cases of histiocytic necrotizing lymphadenitis without granulocytic infiltration (Kikuchi-Fujimoto Disease) are described. All the cases were seen in young women who presented with cervical lymphadenopathy with mild or no fever. Histology of the lymphnode revealed paracortical necrotizing lesions with abundant karyorrhexis. Neutrophils were conspicuous by their absence. Diagnosis of Kikuchi-Fujimoto disease was considered after ruling out connective tissue disorders. Three of the four cases that were followed up showed a self-limiting course. It is important to differentiate this rare cause of febrile disease with enlargement of lymphnodes, from other causes of febrile disease with enlargement of lymphnodes, from other causes of lymphadenopathy, especially lymphoma.

摘要

本文描述了4例无粒细胞浸润的组织细胞坏死性淋巴结炎(菊池-藤本病)。所有病例均为年轻女性,表现为颈部淋巴结肿大,伴有低热或无发热。淋巴结组织学检查显示副皮质区坏死性病变,核碎裂明显。未见中性粒细胞。在排除结缔组织疾病后考虑菊池-藤本病的诊断。随访的4例病例中有3例呈自限性病程。将这种导致发热伴淋巴结肿大的罕见病因与其他导致发热伴淋巴结肿大的病因以及其他淋巴结病病因(尤其是淋巴瘤)区分开来很重要。

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