McKenna C, Whitfield T, Patel N, Bonington A
North West Regional Centre for Infectious Diseases, North Manchester General Hospital, Manchester, UK.
The University of Manchester, Manchester Academic Health Science Centre, North Manchester General Hospital, Manchester, UK.
BMJ Case Rep. 2017 Jan 4;2017:bcr2016217500. doi: 10.1136/bcr-2016-217500.
A 29-year-old British Pakistani woman presented with a 2-month history of drenching fevers, night sweats, lethargy and tender cervical and axillary lymphadenopathy. Initial investigations, bloods and imaging were unremarkable. Fever persisted during her admission, and treatment for tuberculosis (TB) lymphadenitis was started postbiopsy until histology confirmed a diagnosis of Kikuchi-Fujimoto's disease (KFD). KFD has a non-specific presentation of fever, night sweats and lymphadenopathy and commonly raises a clinical suspicion of a number of other serious conditions such as TB, lymphoma, HIV, systemic lupus erythematous, toxoplasmosis and infectious mononucleosis. Although rare, KFD should be considered to be a differential diagnosis for fever of unknown origin and tender lymphadenopathy in otherwise well individuals. This case demonstrates the importance of a timely histological biopsy diagnosis to prevent an incorrect diagnosis and administration of unnecessary medications.
一名29岁的英裔巴基斯坦女性,出现了为期2个月的大汗淋漓型发热、盗汗、乏力以及颈部和腋窝淋巴结压痛。初步检查、血液检查和影像学检查均无异常。她住院期间发热持续,活检后开始针对结核性淋巴结炎进行治疗,直至组织学确诊为菊池-藤本病(KFD)。KFD表现为发热、盗汗和淋巴结病等非特异性症状,临床上通常会引发对多种其他严重疾病的怀疑,如结核病、淋巴瘤、艾滋病毒、系统性红斑狼疮、弓形虫病和传染性单核细胞增多症。尽管罕见,但对于不明原因发热且无其他明显症状仅有淋巴结压痛的个体,KFD应被视为鉴别诊断之一。该病例表明了及时进行组织学活检诊断对于防止误诊和避免使用不必要药物的重要性。