罕见中罕见：菊chi- fujimoto病与结缔组织疾病相关。我们的经验报告。

IF 1 Q4 RHEUMATOLOGY

Reumatismo Pub Date : 2025-08-04 DOI:10.4081/reumatismo.2025.1853

Carmela Coccia, Gemma Lepri, Juela Levani, Silvia Bellando Randone, Serena Guiducci

{"title":"罕见中罕见：菊chi- fujimoto病与结缔组织疾病相关。我们的经验报告。","authors":"Carmela Coccia, Gemma Lepri, Juela Levani, Silvia Bellando Randone, Serena Guiducci","doi":"10.4081/reumatismo.2025.1853","DOIUrl":null,"url":null,"abstract":"Kikuchi-Fujimoto disease (KFD) is a rare and benign lymphadenopathy of unknown etiology. Usually, it is an isolated and self-limiting condition requiring no specific therapy; however, in some cases, it may be associated with an autoimmune disease. Here, we report three cases of KFD developing an associated autoimmune connective disorder: the first case presented with Sjögren's syndrome, and the other two had a diagnosis of systemic lupus erythematosus.","PeriodicalId":21222,"journal":{"name":"Reumatismo","volume":" ","pages":""},"PeriodicalIF":1.0000,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rare in the rare: Kikuchi-Fujimoto disease associated with connective tissue disorders. A report of our experience.\",\"authors\":\"Carmela Coccia, Gemma Lepri, Juela Levani, Silvia Bellando Randone, Serena Guiducci\",\"doi\":\"10.4081/reumatismo.2025.1853\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Kikuchi-Fujimoto disease (KFD) is a rare and benign lymphadenopathy of unknown etiology. Usually, it is an isolated and self-limiting condition requiring no specific therapy; however, in some cases, it may be associated with an autoimmune disease. Here, we report three cases of KFD developing an associated autoimmune connective disorder: the first case presented with Sjögren's syndrome, and the other two had a diagnosis of systemic lupus erythematosus.\",\"PeriodicalId\":21222,\"journal\":{\"name\":\"Reumatismo\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2025-08-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reumatismo\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4081/reumatismo.2025.1853\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reumatismo","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4081/reumatismo.2025.1853","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}

引用次数: 0

摘要

菊池-藤本病（KFD）是一种病因不明的罕见良性淋巴结病。通常，它是一种孤立的自限性疾病，不需要特异性治疗；然而，在某些情况下，它可能与自身免疫性疾病有关。在这里，我们报告了三例KFD发展为相关的自身免疫性结缔组织疾病：第一例表现为Sjögren综合征，另外两例诊断为系统性红斑狼疮。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Rare in the rare: Kikuchi-Fujimoto disease associated with connective tissue disorders. A report of our experience.

Kikuchi-Fujimoto disease (KFD) is a rare and benign lymphadenopathy of unknown etiology. Usually, it is an isolated and self-limiting condition requiring no specific therapy; however, in some cases, it may be associated with an autoimmune disease. Here, we report three cases of KFD developing an associated autoimmune connective disorder: the first case presented with Sjögren's syndrome, and the other two had a diagnosis of systemic lupus erythematosus.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Reumatismo RHEUMATOLOGY-

CiteScore

2.10

自引率

7.10%

发文量

审稿时长

10 weeks

期刊介绍： Reumatismo is the official Journal of the Italian Society of Rheumatology (SIR). It publishes Abstracts and Proceedings of Italian Congresses and original papers concerning rheumatology. Reumatismo is published quarterly and is sent free of charge to the Members of the SIR who regularly pay the annual fee. Those who are not Members of the SIR as well as Corporations and Institutions may also subscribe to the Journal.