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菊池-藤本病:不明原因发热和颈部淋巴结病的罕见病因。

Kikuchi-Fujimoto Disease: A Rare Cause of Pyrexia of Unknown Origin and Cervical Lymphadenopathy.

作者信息

Fadul Abdalla, Subahi Eihab A, Ali Elrazi A, Awadalkareem Habeeb, Mohamed Gihan, Elawad Mohamed, Sharaf Eldean Mohammad, Albozom Adel

机构信息

Internal Medicine, Hamad Medical Corporation, Doha, QAT.

Internal Medicine, One Brooklyn Health/Interfaith Medical Center, Brooklyn, USA.

出版信息

Cureus. 2022 Oct 29;14(10):e30823. doi: 10.7759/cureus.30823. eCollection 2022 Oct.

DOI:10.7759/cureus.30823
PMID:36451640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9703205/
Abstract

Kikuchi-Fujimoto disease (KFD) is a benign disorder characterized by regional cervical lymphadenopathy with tenderness. Associated symptoms of KFD include low-grade fever, night sweats, weight loss, nausea, and sore throat. The disease is a sporadic disease known to have a worldwide distribution with a higher prevalence among Asian communities. Although the clinical and histopathological features point to a viral etiology, this hypothesis has not been proven yet. Generally, the diagnosis is made based on a lymph node excisional biopsy. Its recognition is crucial mainly because this disease can be mistaken for other disorders, including systemic lupus erythematosus or malignant lymphoma. Supportive treatment includes antipyretics, non-steroidal anti-inflammatory drugs, and corticosteroids. Spontaneous recovery occurs within a few weeks. Patients should be followed up for years to survey because there is a possibility of developing systemic lupus erythematosus. In this article, we report the case of a patient who presented with a fever of unknown origin and lymphadenopathy, treated with multiple antibiotic courses with no improvement. Workup including computed tomography of the neck with contrast and lymph node biopsy confirmed the diagnosis of KFD. His condition improved after administering analgesics and multivitamins, and he was advised to rest at home.

摘要

菊池-藤本病(KFD)是一种良性疾病,其特征为颈部区域性淋巴结病伴压痛。KFD的相关症状包括低热、盗汗、体重减轻、恶心和咽痛。该疾病为散发性疾病,已知在全球范围内均有分布,在亚洲人群中患病率较高。尽管临床和组织病理学特征提示病毒病因,但这一假说尚未得到证实。一般而言,诊断基于淋巴结切除活检。认识到这种疾病很关键,主要是因为它可能被误诊为其他疾病,包括系统性红斑狼疮或恶性淋巴瘤。支持性治疗包括退烧药、非甾体抗炎药和皮质类固醇。数周内可自发恢复。患者应接受数年随访观察,因为有发展为系统性红斑狼疮的可能性。在本文中,我们报告了一例以不明原因发热和淋巴结病就诊的患者,接受多个疗程抗生素治疗后无改善。包括颈部增强计算机断层扫描和淋巴结活检在内的检查确诊为KFD。给予镇痛药和多种维生素后病情改善,建议其在家休息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/8b664b9d779a/cureus-0014-00000030823-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/7f1321b4897d/cureus-0014-00000030823-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/b56b4d3b3763/cureus-0014-00000030823-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/b37fe25a5242/cureus-0014-00000030823-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/8b664b9d779a/cureus-0014-00000030823-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/7f1321b4897d/cureus-0014-00000030823-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/b56b4d3b3763/cureus-0014-00000030823-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/b37fe25a5242/cureus-0014-00000030823-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7648/9703205/8b664b9d779a/cureus-0014-00000030823-i04.jpg

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本文引用的文献

1
Kikuchi-Fujimoto Disease: A Rare Benign Cause of Lymphadenopathy That Mimics Malignant Lymphoma.菊池-藤本病:一种罕见的良性淋巴结病病因,酷似恶性淋巴瘤。
Cureus. 2022 Mar 15;14(3):e23177. doi: 10.7759/cureus.23177. eCollection 2022 Mar.
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Kikuchi-Fujimoto Disease: A Rare Cause of Cervical Lymphadenopathy.菊池-藤本病:颈部淋巴结病的罕见病因。
Cureus. 2021 Aug 9;13(8):e17021. doi: 10.7759/cureus.17021. eCollection 2021 Aug.
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Case Report of Kikuchi-Fujimoto Disease from Sub-Saharan Africa: An Important Mimic of Tuberculous Lymphadenitis.
来自撒哈拉以南非洲的菊池-藤本病病例报告:一种重要的结核性淋巴结炎模仿病。
Case Rep Med. 2020 Jan 5;2020:4385286. doi: 10.1155/2020/4385286. eCollection 2020.
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Kikuchi-Fujimoto disease associated with systemic lupus erythematosus complicated with hemophagocytic lymphohistiocytosis: a case report.伴系统性红斑狼疮并发噬血细胞性淋巴组织细胞增生症的菊池-藤本病:一例报告
J Med Case Rep. 2019 Jun 6;13(1):173. doi: 10.1186/s13256-019-2100-1.
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Kikuchi-Fujimoto Disease: An Atypical Presentation of a Rare Disease.菊池-藤本病:一种罕见疾病的非典型表现。
Cureus. 2019 Feb 1;11(2):e3999. doi: 10.7759/cureus.3999.
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Clin Med Insights Ear Nose Throat. 2019 Feb 27;12:1179550619828680. doi: 10.1177/1179550619828680. eCollection 2019.
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Kikuchi-fujimoto disease in the United States: three case reports and review of the literature [corrected].美国的菊池-藤本病:三例病例报告及文献复习[更正]。
Mediterr J Hematol Infect Dis. 2014 Jan 1;6(1):e2014001. doi: 10.4084/MJHID.2014.001.
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Recurrent aseptic meningitis in association with Kikuchi-Fujimoto disease: case report and literature review.与菊池-藤本病相关的复发性无菌性脑膜炎:病例报告及文献复习。
BMC Neurol. 2012 Sep 29;12:112. doi: 10.1186/1471-2377-12-112.
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Semin Arthritis Rheum. 2012 Jun;41(6):900-6. doi: 10.1016/j.semarthrit.2011.11.001. Epub 2011 Dec 20.
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Case Rep Med. 2011;2011:230840. doi: 10.1155/2011/230840. Epub 2011 Aug 14.