嗜血球性淋巴组织细胞增多症合并结节病一例

V. Marwah, N. Kumar, R. Choudhary, D. Mutreja, Anmol Sharma
{"title":"嗜血球性淋巴组织细胞增多症合并结节病一例","authors":"V. Marwah, N. Kumar, R. Choudhary, D. Mutreja, Anmol Sharma","doi":"10.4103/jalh.jalh_8_23","DOIUrl":null,"url":null,"abstract":"Sarcoidosis is a chronic granulomatous disorder often misdiagnosed as tuberculosis. Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal complication linked to extensive hemophagocytosis and hyperinflammatory response. Cases of sarcoidosis developing HLH are rarely documented and difficult to diagnose. We present the case of a 63-year-old female with sarcoidosis complicated with HLH, successfully managed at our center.","PeriodicalId":402083,"journal":{"name":"Journal of Advanced Lung Health","volume":"6 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A rare case of hemophagocytic lymphohistiocytosis associated with sarcoidosis\",\"authors\":\"V. Marwah, N. Kumar, R. Choudhary, D. Mutreja, Anmol Sharma\",\"doi\":\"10.4103/jalh.jalh_8_23\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Sarcoidosis is a chronic granulomatous disorder often misdiagnosed as tuberculosis. Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal complication linked to extensive hemophagocytosis and hyperinflammatory response. Cases of sarcoidosis developing HLH are rarely documented and difficult to diagnose. We present the case of a 63-year-old female with sarcoidosis complicated with HLH, successfully managed at our center.\",\"PeriodicalId\":402083,\"journal\":{\"name\":\"Journal of Advanced Lung Health\",\"volume\":\"6 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Advanced Lung Health\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/jalh.jalh_8_23\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advanced Lung Health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jalh.jalh_8_23","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

结节病是一种慢性肉芽肿性疾病,常被误诊为肺结核。噬血细胞性淋巴组织细胞增多症(HLH)是一种潜在的致命并发症,与广泛的噬血细胞增多和高炎症反应有关。结节病发展为HLH的病例很少有记录,而且很难诊断。我们报告一例63岁女性结节病合并HLH,在我们中心成功治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of hemophagocytic lymphohistiocytosis associated with sarcoidosis
Sarcoidosis is a chronic granulomatous disorder often misdiagnosed as tuberculosis. Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal complication linked to extensive hemophagocytosis and hyperinflammatory response. Cases of sarcoidosis developing HLH are rarely documented and difficult to diagnose. We present the case of a 63-year-old female with sarcoidosis complicated with HLH, successfully managed at our center.
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
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信