最近报道一例不熟悉的菊chi-藤本病

J. Kaur, A. K. Wani, B. K. Yadav, Bhuban Subedi
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引用次数: 1

摘要

菊池-藤本病(KFD)也被称为组织细胞坏死性淋巴结炎。它是一种非常罕见的非癌性和自限性自身免疫性疾病,但大多数怀疑为癌症,结核病和系统性红斑狼疮。它的症状包括颈部淋巴结肿大、低烧、头痛、疲劳、盗汗和肌肉疼痛。它通常影响20-35岁的年轻女性,主要影响亚洲人群。正确鉴别KFD的特点是细针抽吸细胞学,从肿胀的淋巴结取血样。细针穿刺活检也可诊断。这种疾病的治疗方法尚未确定。非甾体抗炎药或类固醇用于缓解淋巴结的压痛和发烧。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Recent Case Reports on Unfamiliar Kikuchi-Fujimoto Disease
Kikuchi-Fujimoto Disease (KFD) also known by a name called Histiocytic Necrotizing Lymphadenitis. It is very rare, non-cancerous and self-limiting Auto-Immune disease but most suspected as to be cancer, tuberculosis and systemic lupus erythematosus. It has symptoms such as cervical lymphadenopathy (enlargement of lymph nodes), low fever, headache, fatigue, night sweats, and muscles pain. It typically affects young females aged between 20-35 years and it mostly affects Asian populations. The correct identification of KFD is characterized by Fine Needle Aspiration Cytology by taking a blood sample from the swollen lymph node. Diagnosis is also possible with Fine Needle Aspiration Biopsy. Treatment for this disease has not been established. Non-steroidal Anti-Inflammatory Drugs or steroids are in use to ease tenderness of lymph node and fever.
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