Parveen R, Rahman S H, Yasmin R, Quadir M S, Muazzam N, Alam M N
Dhaka Medical College, and Department of Immunology & Molecular Biology, National Institute of Cancer Research & Hospital, Dhaka, Bangladesh.
Mymensingh Med J. 2009 Jan;18(1):95-8.
A 14 year-old Bangladeshi girl presented with high fever, painful swellings in the neck, anorexia, weight loss and night sweating. On examination she had multiple enlarged and tender cervical lymph nodes. Other systems were normal. Laboratory investigations for sepsis and autoimmune diseases were negative. Initial fine needle aspiration and cytology of affected lymph node was suggestive of tubercular lymphdenitis. But she did not respond to anti-tubercular treatment. Kikuchi-Fujimoto disease was diagnosed from the histopathological appearance of excised lymph node. She completely recovered with symptomatic treatment. Kikuchi-Fujimoto disease, also called Kikuchi's disease or histiocytic necrotizing lymphadenitis is a rare, benign but enigmatic disease of unknown aetiology. The disease is self-limited and has an excellent prognosis. Its recognition is crucial because it can be mistaken for systemic lupus erythematosus, malignant lymphoma, tubercular lymphadenitis or even, for metastatic adenocarcinoma. Clinicians' and pathologists' awareness of this disease may help prevent misdiagnosis and inappropriate treatment.
一名14岁的孟加拉女孩出现高热、颈部疼痛性肿胀、厌食、体重减轻和盗汗症状。检查发现她有多个肿大且触痛的颈部淋巴结。其他系统正常。败血症和自身免疫性疾病的实验室检查均为阴性。最初对受累淋巴结进行的细针穿刺和细胞学检查提示为结核性淋巴结炎。但她对抗结核治疗无反应。根据切除淋巴结的组织病理学表现诊断为菊池-藤本病。经对症治疗后她完全康复。菊池-藤本病,也称为菊池病或组织细胞坏死性淋巴结炎,是一种病因不明的罕见、良性但神秘的疾病。该疾病具有自限性,预后良好。认识到这种疾病至关重要,因为它可能被误诊为系统性红斑狼疮、恶性淋巴瘤、结核性淋巴结炎,甚至转移性腺癌。临床医生和病理学家对这种疾病的认识可能有助于防止误诊和不恰当的治疗。