菊池藤本病：一种罕见的孤立性腹部淋巴结炎

Pub Date : 2017-12-01 DOI:10.12816/0047779

O. Sharaf, A. Ali

{"title":"菊池藤本病：一种罕见的孤立性腹部淋巴结炎","authors":"O. Sharaf, A. Ali","doi":"10.12816/0047779","DOIUrl":null,"url":null,"abstract":"Kikuchi-Fujimoto Disease (KFD) is a rare and benign cause of lymphadenopathy that is often associated with fever, night sweats and weight loss. The clinical and laboratory manifestations of KFD are similar to those of lymphoma, tuberculosis, sarcoidosis and systemic lupus erythematosus. Definitive diagnosis is accomplished by lymph node biopsy6,7. Awareness of KFD among clinicians and pathologists is essential to avoid misdiagnosis and inappropriate treatment of this self-limited disorder.","PeriodicalId":0,"journal":{"name":"","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2017-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Kikuchi-Fujimoto Disease : An Unusual Presentation with Isolated Abdominal Lymphadenitis\",\"authors\":\"O. Sharaf, A. Ali\",\"doi\":\"10.12816/0047779\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Kikuchi-Fujimoto Disease (KFD) is a rare and benign cause of lymphadenopathy that is often associated with fever, night sweats and weight loss. The clinical and laboratory manifestations of KFD are similar to those of lymphoma, tuberculosis, sarcoidosis and systemic lupus erythematosus. Definitive diagnosis is accomplished by lymph node biopsy6,7. Awareness of KFD among clinicians and pathologists is essential to avoid misdiagnosis and inappropriate treatment of this self-limited disorder.\",\"PeriodicalId\":0,\"journal\":{\"name\":\"\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0,\"publicationDate\":\"2017-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12816/0047779\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12816/0047779","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 0

摘要

菊池藤本病（KFD）是一种罕见的良性淋巴结病，通常与发烧、盗汗和体重减轻有关。KFD的临床和实验室表现与淋巴瘤、肺结核、结节病和系统性红斑狼疮相似。通过淋巴结活检完成最终诊断6,7。临床医生和病理学家对KFD的认识对于避免这种自我限制性疾病的误诊和不当治疗至关重要。

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

Kikuchi-Fujimoto Disease : An Unusual Presentation with Isolated Abdominal Lymphadenitis

Kikuchi-Fujimoto Disease (KFD) is a rare and benign cause of lymphadenopathy that is often associated with fever, night sweats and weight loss. The clinical and laboratory manifestations of KFD are similar to those of lymphoma, tuberculosis, sarcoidosis and systemic lupus erythematosus. Definitive diagnosis is accomplished by lymph node biopsy6,7. Awareness of KFD among clinicians and pathologists is essential to avoid misdiagnosis and inappropriate treatment of this self-limited disorder.

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