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青年女性罕见的菊池-古imoto 病病例报告。

A Rare Case of Kikuchi-Fujimoto Disease in a Young Female Patient.

机构信息

Department of Respiratory Medicine, Hanoi Medical University Hospital, Hanoi, Vietnam.

Diagnostic Imaging and Interventional Radiology Center, Hanoi Medical University Hospital, Hanoi, Vietnam.

出版信息

Am J Case Rep. 2021 Nov 21;22:e933377. doi: 10.12659/AJCR.933377.

Abstract

BACKGROUND Kikuchi-Fujimoto disease (KFD) is a rare benign and usually local lymphadenopathy that typically occurs in young women. Patients with it usually have non-specific symptoms, such as fever in the afternoon, cervical lymphadenitis, and weight loss. Posterior cervical lymphadenopathy is the most common manifestation of KFD. The symptoms often last for a few weeks and then resolve spontaneously. The cause of KFD is unknown; however, it is considered to be related to some infectious agents, as well as several autoimmune diseases. Because of the non-specific symptoms and the rarity of KFD, the cervical lymphadenopathy associated with it can be misdiagnosed as coming from a more common condition. Making a correct diagnosis requires histology of the affected lymph nodes. CASE REPORT Here, we describe the case of a 25-year-old Vietnamese woman who presented with mild fever in the afternoons and enlarged cervical lymph nodes with no local sign of inflammation. She was initially believed to have tubercular lymphadenitis because of her symptoms and the high prevalence of tuberculosis in Vietnam. However, she had no respiratory symptoms and tested negative on QuantiFERON-TB Gold. Pathology from the patient's lymph node specimen showed an abnormal inflammatory reaction in the tissue. Her lesions were suspected to have been caused by KFD and she was treated successfully with nonsteroidal anti-inflammatory drug (NSAID) therapy. CONCLUSIONS KFD is a benign disease that manifests with common symptoms. The diagnosis is based on biopsy of a specimen and pathology results. No treatment is required in patients who have no symptoms. Patients with symptoms usually respond well to a short course of NSAID therapy.

摘要

背景

Kikuchi-Fujimoto 病(KFD)是一种罕见的良性且通常为局部淋巴结病,主要发生在年轻女性中。患者通常有非特异性症状,如午后发热、颈淋巴结炎和体重减轻。颈后淋巴结病是 KFD 最常见的表现。症状通常持续数周,然后自行缓解。KFD 的病因不明;然而,它被认为与某些感染因子以及几种自身免疫性疾病有关。由于症状不特异且 KFD 罕见,因此与之相关的颈淋巴结病可能被误诊为更常见的疾病。做出正确的诊断需要受累淋巴结的组织学检查。

病例报告

这里,我们描述了一名 25 岁越南女性的病例,她表现为午后轻度发热和颈淋巴结肿大,无局部炎症迹象。由于她的症状和越南结核病的高患病率,她最初被认为患有结核性淋巴结炎。然而,她没有呼吸道症状,并且 QuantiFERON-TB Gold 检测结果为阴性。患者淋巴结标本的病理学显示组织中存在异常炎症反应。她的病变被怀疑是由 KFD 引起的,她成功地接受了非甾体抗炎药(NSAID)治疗。

结论

KFD 是一种表现出常见症状的良性疾病。诊断基于活检标本和病理学结果。无症状患者无需治疗。有症状的患者通常对短期 NSAID 治疗反应良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b07/8614063/40b909ca857b/amjcaserep-22-e933377-g001.jpg

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