Mohamad Ahmed A, Zahid Muhammad, Khan Adeel Ahmad, Alani Belal, Khalil Mustafa, Saeed Abazar, Elzouki Abdel-Naser
Department of Internal Medicine, Hamad General Hospital and Weil Cornell Medical College, Doha, Qatar.
Department of Internal Medicine, Hamad General Hospital, Doha, Qatar.
Eur J Case Rep Intern Med. 2020 Apr 10;7(6):001598. doi: 10.12890/2020_001598. eCollection 2020.
Kikuchi-Fujimoto (KF) disease is a rare and self-limiting disorder of unknown aetiology characterized by cervical lymphadenopathy (CLN) and fever. The pathophysiology remains unclear and may be triggered by an infectious agent leading to a self-limiting autoimmune process. There are no confirmatory laboratory tests and lymph node biopsy is required to differentiate KF disease from other serious conditions.
We report 11 cases of KF disease diagnosed at Hamad General Hospital, Qatar, between 2006 to 2016. The diagnosis is based on clinical presentation, investigations and histopathological examination of lymph nodes.
All patients had painful neck swelling (average duration of 2.9 weeks) and 10 had fever (average duration of 3.2 weeks). Five patients developed mild leucopenia which resolved completely. HIV and tuberculosis (TB) screening including sputum for AFB, a PPD skin test and chest x-ray was done for all patients and came back negative. Autoimmune screening was done for all patients and excluded any rheumatological disease. Ultrasound and CT of the neck confirmed cervical lymphadenopathy. Except for hepatomegaly in one patient, CT scans of the chest and abdomen were negative for any lymphadenopathy or organomegaly (performed in seven patients). Diagnosis was confirmed on lymph node excision biopsy. Histopathological examination showed findings consistent with the diagnosis of histiocytic necrotizing lymphadenitis (KF disease).
KF disease should be kept in mind for patients presenting with fever and CLN. Lymphoma, TB and autoimmune diseases like systemic lupus erythematosus should be excluded in such patients. Kikuchi-Fujimoto (KF) disease should be kept in mind in patients presenting with fever and cervical lymphadenopathy with or without other constitutional symptoms.There are no confirmatory blood tests and KF disease requires histopathological examination of involved lymph nodes for confirmation.Autoimmune disease like systemic lupus erythematosus, tuberculosis, lymphoma and other malignancies should be ruled out by appropriate investigations.Recurrence of disease, although rare, is a possibility and needs histopathology for confirmation.
菊池-藤本病(KF病)是一种病因不明的罕见自限性疾病,其特征为颈部淋巴结病(CLN)和发热。其病理生理学仍不清楚,可能由感染因子引发,导致自限性自身免疫过程。目前尚无确诊的实验室检查,需要进行淋巴结活检以将KF病与其他严重疾病区分开来。
我们报告了2006年至2016年期间在卡塔尔哈马德总医院诊断出的11例KF病病例。诊断基于临床表现、检查以及淋巴结的组织病理学检查。
所有患者均有颈部疼痛性肿胀(平均持续时间2.9周),10例患者有发热(平均持续时间3.2周)。5例患者出现轻度白细胞减少,随后完全缓解。对所有患者进行了包括痰涂片找抗酸杆菌、结核菌素皮肤试验和胸部X线检查在内的HIV和结核病(TB)筛查,结果均为阴性。对所有患者进行了自身免疫筛查,排除了任何风湿性疾病。颈部超声和CT证实存在颈部淋巴结病。除1例患者有肝肿大外,胸部和腹部CT扫描对任何淋巴结病或器官肿大均为阴性(7例患者进行了此项检查)。通过淋巴结切除活检确诊。组织病理学检查结果与组织细胞坏死性淋巴结炎(KF病)的诊断一致。
对于出现发热和CLN的患者应考虑KF病。此类患者应排除淋巴瘤、结核病和系统性红斑狼疮等自身免疫性疾病。对于出现发热和颈部淋巴结病(无论有无其他全身症状)的患者应考虑菊池-藤本病(KF病)。目前尚无确诊的血液检查,KF病需要对受累淋巴结进行组织病理学检查以确诊。应通过适当检查排除系统性红斑狼疮等自身免疫性疾病、结核病、淋巴瘤和其他恶性肿瘤。疾病复发虽然罕见,但仍有可能,需要组织病理学检查来确诊。