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一名患有菊池-藤本病的儿科患者的视神经炎:病例报告及文献综述

Optic Neuritis in a Pediatric Patient with Kikuchi-Fujimoto Disease: A Case Report and Review of the Literature.

作者信息

Bao Shengfang, Huang Hua, Jin Yingying, Ding Fei, Yang Zhen, Xu Xuemei, Liu Chenxi, Han Xiqiong, Wang Liping, Lu Jingyi, Ma Jiani, Jin Yanliang

机构信息

Department of Rheumatology & Immunology, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, People's Republic of China.

出版信息

J Inflamm Res. 2024 May 9;17:2889-2895. doi: 10.2147/JIR.S458990. eCollection 2024.

DOI:10.2147/JIR.S458990
PMID:38751686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11094741/
Abstract

Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare, benign, and self-limiting condition characterized by lymph node inflammation. While KFD is rarely associated with ocular manifestations, our case report highlights bilateral optic neuritis in a 13-year-old male patient with KFD. We also provide a comprehensive review of similar cases in the literature.

摘要

菊池-藤本病(KFD),也称为组织细胞坏死性淋巴结炎,是一种罕见的、良性的、自限性疾病,其特征为淋巴结炎症。虽然KFD很少与眼部表现相关,但我们的病例报告强调了一名患有KFD的13岁男性患者出现双侧视神经炎。我们还对文献中类似病例进行了全面综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c71/11094741/031916a3c3e6/JIR-17-2889-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c71/11094741/a0451921fff7/JIR-17-2889-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c71/11094741/3e449a5b4e56/JIR-17-2889-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c71/11094741/031916a3c3e6/JIR-17-2889-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c71/11094741/a0451921fff7/JIR-17-2889-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c71/11094741/3e449a5b4e56/JIR-17-2889-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c71/11094741/031916a3c3e6/JIR-17-2889-g0003.jpg

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Transl Pediatr. 2024 Oct 1;13(10):1892-1898. doi: 10.21037/tp-24-380. Epub 2024 Oct 28.

本文引用的文献

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World J Clin Cases. 2023 Jun 6;11(16):3664-3679. doi: 10.12998/wjcc.v11.i16.3664.
2
Optic neuritis: current challenges in diagnosis and management.视神经炎:诊断与管理中的当前挑战
Curr Opin Neurol. 2023 Feb 1;36(1):10-18. doi: 10.1097/WCO.0000000000001128. Epub 2022 Dec 5.
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Kikuchi-Fujimoto disease as the initial manifestation of systemic lupus erythematosus complicated with macrophage activation syndrome: two case reports and a review of literature.
以菊池古氏病为首发表现的系统性红斑狼疮合并巨噬细胞活化综合征 2 例并文献复习
BMC Pediatr. 2022 Nov 22;22(1):673. doi: 10.1186/s12887-022-03703-6.
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Multiple sclerosis progression: time for a new mechanism-driven framework.多发性硬化症的进展:是时候建立一个新的基于机制的框架了。
Lancet Neurol. 2023 Jan;22(1):78-88. doi: 10.1016/S1474-4422(22)00289-7. Epub 2022 Nov 18.
5
The causal relationship between neuromyelitis optica spectrum disorder and other autoimmune diseases.视神经脊髓炎谱系疾病与其他自身免疫性疾病的因果关系。
Front Immunol. 2022 Sep 29;13:959469. doi: 10.3389/fimmu.2022.959469. eCollection 2022.
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Diagnosis and treatment of progressive multiple sclerosis: A position paper.进展性多发性硬化症的诊断和治疗:立场文件。
Eur J Neurol. 2023 Jan;30(1):9-21. doi: 10.1111/ene.15593. Epub 2022 Oct 25.
7
Optic neuritis and autoimmune optic neuropathies: advances in diagnosis and treatment.视神经炎与自身免疫性视神经病变:诊断与治疗进展
Lancet Neurol. 2023 Jan;22(1):89-100. doi: 10.1016/S1474-4422(22)00187-9. Epub 2022 Sep 22.
8
Clinical Application of Metagenomic Next-Generation Sequencing for Suspected Infections in Patients With Primary Immunodeficiency Disease.宏基因组下一代测序在原发性免疫缺陷病疑似感染患者中的临床应用。
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Update on Pediatric Optic Neuritis.儿童视神经炎的最新进展。
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