Mycobacterium kansasii chronic olecranon bursitis: A rare case report and literature review

IF 1 Q4 INFECTIOUS DISEASES
IDCases Pub Date : 2025-01-01 DOI:10.1016/j.idcr.2025.e02326
Siddartha Guru , Jyoti Saroya , Navami Guru , Poonam Bai
{"title":"Mycobacterium kansasii chronic olecranon bursitis: A rare case report and literature review","authors":"Siddartha Guru ,&nbsp;Jyoti Saroya ,&nbsp;Navami Guru ,&nbsp;Poonam Bai","doi":"10.1016/j.idcr.2025.e02326","DOIUrl":null,"url":null,"abstract":"<div><div>Non-tuberculous mycobacteria are a rare cause of olecranon bursitis. We present a case of a 65-year-old man with history of chronic olecranon bursitis status post bursectomy two years prior, presented with two weeks of right elbow swelling but no pain or redness. On exam, bursa was enlarged with mild warmth present but no concern for elbow joint involvement. The bursa was aspirated, fluid analysis revealed leukocytosis with monosodium urate crystals consistent with gout. Ten days later, the mycobacterial cultures grew <em>Mycobacterium kansasii</em>. Two weeks later, on repeat aspiration of right elbow bursa, fluid cultures grew <em>M. kansasii</em>. He was treated with rifampin, ethambutol and azithromycin. After two months on triple therapy his symptoms resolved. For source control he underwent bursectomy. Histopathology revealed necrotizing granulomas and bursa culture grew <em>M. kansasii</em>. After six months on triple therapy, patient developed ethambutol induced optic neuropathy, thus ethambutol was stopped. Rifampin and azithromycin were continued for total duration of eight months of antibiotic therapy post bursectomy. At six months follow up, patient had no symptoms but vision deficits had not improved from cessation of ethambutol. We did a literature review and compiled the previously three reported cases of <em>M. kansasii</em> olecranon bursitis.</div></div>","PeriodicalId":47045,"journal":{"name":"IDCases","volume":"41 ","pages":"Article e02326"},"PeriodicalIF":1.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IDCases","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214250925001829","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Non-tuberculous mycobacteria are a rare cause of olecranon bursitis. We present a case of a 65-year-old man with history of chronic olecranon bursitis status post bursectomy two years prior, presented with two weeks of right elbow swelling but no pain or redness. On exam, bursa was enlarged with mild warmth present but no concern for elbow joint involvement. The bursa was aspirated, fluid analysis revealed leukocytosis with monosodium urate crystals consistent with gout. Ten days later, the mycobacterial cultures grew Mycobacterium kansasii. Two weeks later, on repeat aspiration of right elbow bursa, fluid cultures grew M. kansasii. He was treated with rifampin, ethambutol and azithromycin. After two months on triple therapy his symptoms resolved. For source control he underwent bursectomy. Histopathology revealed necrotizing granulomas and bursa culture grew M. kansasii. After six months on triple therapy, patient developed ethambutol induced optic neuropathy, thus ethambutol was stopped. Rifampin and azithromycin were continued for total duration of eight months of antibiotic therapy post bursectomy. At six months follow up, patient had no symptoms but vision deficits had not improved from cessation of ethambutol. We did a literature review and compiled the previously three reported cases of M. kansasii olecranon bursitis.
堪萨斯分枝杆菌慢性鹰嘴滑囊炎1例报告及文献复习
非结核分枝杆菌是鹰嘴滑囊炎的罕见病因。我们报告一个65岁的男性病例,在两年前的滑囊切除术后,有慢性鹰嘴滑囊炎的病史,表现为两周的右肘肿胀,但没有疼痛或发红。检查时,滑囊肿大,伴有轻度发热,但未累及肘关节。粘液囊被抽吸,液体分析显示白细胞增多,伴有尿酸钠结晶,与痛风相符。10天后,分枝杆菌培养出了堪萨斯分枝杆菌。两周后,重复抽吸右肘囊,液体培养培养出堪萨斯分枝杆菌。他接受了利福平、乙胺丁醇和阿奇霉素的治疗。经过两个月的三联疗法,他的症状消失了。为了控制病源,他接受了法氏囊切除术。组织病理学显示坏死肉芽肿和粘液囊培养生长的堪萨斯分枝杆菌。三联治疗6个月后,患者出现乙胺丁醇诱发的视神经病变,因此停用乙胺丁醇。利福平和阿奇霉素在法氏囊切除术后持续8个月的抗生素治疗。随访6个月,患者无症状,但视力减退未因停止使用乙胺丁醇而改善。我们对既往报道的3例堪萨斯分枝杆菌鹰嘴滑囊炎病例进行了文献回顾和整理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
IDCases
IDCases INFECTIOUS DISEASES-
CiteScore
2.60
自引率
6.70%
发文量
300
审稿时长
10 weeks
×
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