Sharma Kusum, Gautam Natasha, Sharma Megha, Dogra Mohit, Bajgai Priya, Tigari Basavaraj, Sharma Aman, Gupta Vishali, Sharma Surya Prakash, Singh Ramandeep
Department of Microbiology, Post Graduate Institute of Medical Education and Research, Sector 12, Chandigarh, India.
Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Sector 12, Chandigarh, 160012, India.
J Ophthalmic Inflamm Infect. 2017 Dec;7(1):2. doi: 10.1186/s12348-016-0121-0. Epub 2017 Jan 13.
We report unfavorable outcome in a patient with subretinal granuloma caused by dual infection of Mycobacterium tuberculosis complex with Mycobacterium fortuitum and Mycobacterium bovis in an immunosuppressed, non-HIV patient. We did a systematic review of literature on dual infection due to M. tuberculosis and M. fortuitum via MEDLINE and PUBMED and could not find any case reported of causing this kind of dual infection in the eye.
A 38-year-old Indian male patient presented with decreased vision in the left eye for 3 months, diagnosed as tubercular choroidal granuloma with associated retinal angiomatosis proliferans (RAP) lesion. He also had multiple enlarged lymph nodes in the chest, and sternal pus sample was positive for acid-fast bacilli (AFB). M. tuberculosis complex was detected by gene expert. The patient was started on antitubercular treatment (ATT) whereby the lung lesions improved but the ocular lesion showed initial clinical improvement followed by worsening. Twenty-five-gauge diagnostic pars plana core vitreous surgery was done whereby sample demonstrated a large number of AFB on Ziehl-Neelsen stain and auramine-rhodamine stain. The vitreous sample showed growth on routinely inoculated mycobacteria growth indicator tube (MGIT) 960 tubes, and multiplex polymerase chain reaction (PCR), Gene Xpert MTB/ RIF assay (Cepheid, Sunnyvale, CA), and line probe assay (LPA) were positive for ocular tuberculosis. In view of nonresponse to conventional ATT, a suspicion of dual infection of M. tuberculosis complex with a nontubercular mycobacteria was kept and a subculture was made onto the solid Lowenstein-Jensen (LJ) medium from the positive MGIT 960 tubes. Two morphologically distinct types of colonies were obtained on LJ slopes. Subsequently, the two etiological agents were identified as M. fortuitum and M. bovis by PCR from the vitreous sample.
Co-infection of M. tuberculosis complex with nontubercular mycobacterium (NTM) has never been reported from ocular tuberculosis before. In immunosuppressed individuals, who test positive for MTB, not responding to the standard ATT, one needs to have a high index of clinical suspicion to rule out associated NTM infection and initiate appropriate multidrug systemic antibiotic therapy early.
我们报告了一例免疫功能低下、非HIV患者因结核分枝杆菌复合群与偶然分枝杆菌和牛分枝杆菌双重感染导致视网膜下肉芽肿的不良预后情况。我们通过MEDLINE和PUBMED对结核分枝杆菌和偶然分枝杆菌双重感染的文献进行了系统综述,未发现任何关于眼部发生这种双重感染的病例报道。
一名38岁的印度男性患者因左眼视力下降3个月就诊,被诊断为结核性脉络膜肉芽肿伴增殖性视网膜血管瘤(RAP)病变。他胸部还有多个肿大的淋巴结,胸骨脓液样本抗酸杆菌(AFB)检测呈阳性。通过基因专家检测出结核分枝杆菌复合群。患者开始接受抗结核治疗(ATT),肺部病变有所改善,但眼部病变最初有临床改善,随后恶化。进行了25G诊断性扁平部玻璃体切除术,样本在萋-尼染色和金胺-罗丹明染色下显示大量AFB。玻璃体样本在常规接种的分枝杆菌生长指示管(MGIT)960管上生长,多重聚合酶链反应(PCR)、Gene Xpert MTB/RIF检测(赛菲德公司,加利福尼亚州森尼韦尔市)和线性探针检测(LPA)眼部结核均呈阳性。鉴于对传统ATT无反应,怀疑结核分枝杆菌复合群与非结核分枝杆菌双重感染,并从阳性MGIT 960管中接种到固体罗氏培养基上进行亚培养。在罗氏斜面上获得了两种形态不同的菌落类型。随后,通过玻璃体样本的PCR鉴定这两种病原体为偶然分枝杆菌和牛分枝杆菌。
此前眼部结核中从未报道过结核分枝杆菌复合群与非结核分枝杆菌(NTM)的合并感染。在结核菌素试验阳性、对标准ATT无反应的免疫功能低下个体中,临床需要高度怀疑以排除相关NTM感染,并尽早启动适当的多药全身抗生素治疗。