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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。

Kikuchi-Fujimoto Disease: A Rare Benign Cause of Lymphadenopathy That Mimics Malignant Lymphoma.

作者信息

Gism Elseed Israa, Osman Haitham, Ahmedfiqi Osman, Najmi Fatima, Al-Hebshi Abdulqader

机构信息

Medicine, Prince Mohammed bin Abdulaziz Hospital, Ministry of National Guard Health Affairs, Madinah, SAU.

Hematology, Prince Mohammed bin Abdulaziz Hospital, Ministry of National Guard Health Affairs, Madinah, SAU.

出版信息

Cureus. 2022 Mar 15;14(3):e23177. doi: 10.7759/cureus.23177. eCollection 2022 Mar.

DOI:10.7759/cureus.23177
PMID:35444918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9009272/
Abstract

Kikuchi-Fujimoto disease (KFD), also called histiocytic necrotizing lymphadenitis, is a benign self-limited disease involving lymph node enlargement with unclear causes and high fever. It was first seen in Japan and has wide array of differentials, and thus it can be confused with other causes of lymphadenitis leading to an incorrect treatment. We describe a case of a 34-year-old man with prolonged painless cervical lymphadenopathy and fever, in whom KFD, that is histiocytic necrotizing lymphadenitis, was diagnosed after the gold standard test of lymph node biopsy. Physical examination, history, and other relevant investigations were performed to rule out infectious and autoimmune causes. For management, prednisone 80mg and hydroxychloroquine were given, which lead to an uneventful full recovery. Our findings were compared to other similar studies conducted in the past. KFD is a self-limited condition that usually resolves by itself. KFD should be considered in the differential diagnosis of lymphadenopathy. An accurate diagnosis requires close collaboration between clinicians and pathologists. Early diagnosis of KFD allows reducing stress caused by alarming symptoms and avoiding unnecessary treatment.

摘要

菊池-藤本病(KFD),又称组织细胞坏死性淋巴结炎,是一种良性自限性疾病,表现为淋巴结肿大且病因不明、伴有高热。该病首次发现于日本,鉴别诊断范围广泛,因此可能与其他导致淋巴结炎的病因相混淆,进而导致治疗错误。我们报告一例34岁男性病例,其有无痛性颈部淋巴结病且持续发热,经淋巴结活检这一金标准检查后诊断为菊池-藤本病,即组织细胞坏死性淋巴结炎。进行了体格检查、病史询问及其他相关检查以排除感染性和自身免疫性病因。治疗方面,给予80mg泼尼松和羟氯喹,患者最终顺利完全康复。我们将研究结果与过去进行的其他类似研究进行了比较。菊池-藤本病是一种自限性疾病,通常可自行缓解。在淋巴结病的鉴别诊断中应考虑菊池-藤本病。准确诊断需要临床医生和病理学家密切合作。菊池-藤本病的早期诊断有助于减轻由警示症状引起的压力并避免不必要的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/aa702c5b2b56/cureus-0014-00000023177-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/e279934324a6/cureus-0014-00000023177-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/f94239a5907a/cureus-0014-00000023177-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/c3a21723fc6e/cureus-0014-00000023177-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/aa702c5b2b56/cureus-0014-00000023177-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/e279934324a6/cureus-0014-00000023177-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/f94239a5907a/cureus-0014-00000023177-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/c3a21723fc6e/cureus-0014-00000023177-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31b2/9009272/aa702c5b2b56/cureus-0014-00000023177-i04.jpg

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Kikuchi-Fujimoto Disease: A Rare Cause of Pyrexia of Unknown Origin and Cervical Lymphadenopathy.菊池-藤本病:不明原因发热和颈部淋巴结病的罕见病因。
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本文引用的文献

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Kikuchi-Fujimoto disease: a case report and the evaluation of diagnostic procedures.菊池-藤本病:一例报告及诊断程序评估。
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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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密歇根州的菊池-藤本病:一例罕见病例报告及文献综述
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