Department of Respiratory Medicine, Nagasaki Harbor Medical Center, 6-39 Shinchi-machi, Nagasaki, 850-8555, Japan.
Second Department of Internal Medicine, Nagasaki University Hospital, 1-7-1 Sakamoto-machi, Nagasaki, Japan.
BMC Pulm Med. 2018 Jan 16;18(1):6. doi: 10.1186/s12890-018-0578-8.
Tuberculosis and cryptococcosis co-infection usually occurs in immunosuppressed patients with impaired cell-mediated immunity. However, there are few reports about such co-infection in non-HIV patients without underlying diseases. Here, we report a case of miliary tuberculosis with co-existing pulmonary cryptococcosis in non-HIV patient without underlying diseases.
An 84-year-old Asian female presented to our hospital with complaints of a 1-week history of abdominal pain and appetite loss. Chest computed tomography (CT) showed diffuse micronodules in random patterns in both lung fields. Liver, skin and bone marrow biopsies showed epithelioid cell granuloma. Polymerase chain reaction of gastric aspirate was positive for Mycobacterium tuberculosis. According to these findings, miliary tuberculosis was suspected and antimycobacterial therapy was initiated. After a 6-month treatment course, chest radiograph showed new multiple nodules in the right middle lung field. Chest CT showed that a right S6 small nodule was increased and new multiple nodules appeared in the right lower lobe. Flexible fiberoptic bronchoscopy was subsequently perfomed. Cytology of the bronchial lavage showed a small number of Periodic acid-Schiff-positive bodies, suggesting Cryptococcus species. Moreover, serum cryptococcal antigen testing was positive. According to these findings, pulmonary cryptococcosis was diagnosed, although the culture was negative. Oral fluconazole therapy was subsequently initiated. After a 6-month treatment course, chest radiograph showed gradual improvement.
Although tuberculosis and cryptococcosis co-infection is relatively rare in immunocompromised hosts, such as those with acquired immunodeficiency syndrome, clinicians should be aware that these infections can co-exist even in non-HIV patients without underlying diseases.
结核病和隐球菌病合并感染通常发生在细胞免疫受损的免疫抑制患者中。然而,在没有基础疾病的非 HIV 患者中,此类合并感染的报道很少。本文报告了一例非 HIV 患者无基础疾病时发生的粟粒性肺结核合并肺隐球菌病。
一名 84 岁亚裔女性因腹痛和食欲减退 1 周来我院就诊。胸部计算机断层扫描(CT)显示双肺野呈随机分布的弥漫性微结节。肝、皮肤和骨髓活检显示上皮样细胞肉芽肿。胃抽吸物聚合酶链反应检测结核分枝杆菌阳性。根据这些发现,怀疑为粟粒性肺结核,并开始抗分枝杆菌治疗。6 个月疗程后,胸片显示右中肺野出现新的多个结节。胸部 CT 显示右 S6 小结节增大,右下肺出现多个新结节。随后进行了软性纤维支气管镜检查。支气管灌洗液细胞学检查显示少量过碘酸雪夫阳性体,提示为隐球菌属。此外,血清隐球菌抗原检测阳性。根据这些发现,诊断为肺隐球菌病,尽管培养结果为阴性。随后开始口服氟康唑治疗。6 个月疗程后,胸片显示逐渐改善。
尽管结核病和隐球菌病合并感染在免疫功能低下的宿主中较为罕见,如获得性免疫缺陷综合征患者,但临床医生应意识到,即使在没有基础疾病的非 HIV 患者中,这些感染也可能同时存在。