Zheng Jun, Pan Xiaohong, Jiang Yiyun
Department of Rehabilitation, Nanxing Health Service Center, Shangcheng, Hangzhou, Zhejiang, 310000, People's Republic of China.
Tuberculosis Care Unit, Hospital of Integrated Traditional Chinese and Western Medicine, Zhejiang, 310003, People's Republic of China.
Infect Drug Resist. 2024 Aug 17;17:3593-3598. doi: 10.2147/IDR.S477180. eCollection 2024.
Thrombotic thrombocytopenic purpura is a rare but life-threatening emergency. Tuberculosis can have hematologic complications. However, concurrent tuberculosis and thrombotic thrombocytopenic purpura are extremely rare. In this study, we report a 53-year-old man who was initially treated for pulmonary tuberculosis but later developed weakness and an altered mental status. Laboratory tests revealed evidence of thrombocytopenia, acute renal insufficiency, and microangiopathic hemolytic anemia. Brain imaging identified intracranial hemorrhage. Further testing revealed low ADAMTS13 activity (1.8%) and positive anti-ADAMTS13 antibody, confirming the diagnosis of thrombotic thrombocytopenic purpura. The patient had a full recovery after anti-tuberculosis treatment, plasma exchange, and supportive care. We present this rare case and review previous relevant studies to remind clinicians about the potential connections between tuberculosis and thrombotic thrombocytopenic purpura. In patients with signs of severe thrombocytopenia and microangiopathic hemolysis, necessary diagnostic tests should be performed to eliminate the possibility of thrombotic thrombocytopenic purpura occurring concurrently with tuberculosis.
血栓性血小板减少性紫癜是一种罕见但危及生命的急症。结核病可出现血液学并发症。然而,结核病与血栓性血小板减少性紫癜并发极为罕见。在本研究中,我们报告了一名53岁男性,最初因肺结核接受治疗,但后来出现乏力和精神状态改变。实验室检查显示有血小板减少、急性肾功能不全和微血管病性溶血性贫血的证据。脑部影像学检查发现颅内出血。进一步检查显示ADAMTS13活性低(1.8%)且抗ADAMTS13抗体阳性,确诊为血栓性血小板减少性紫癜。该患者在抗结核治疗、血浆置换及支持治疗后完全康复。我们展示此罕见病例并回顾既往相关研究,以提醒临床医生注意结核病与血栓性血小板减少性紫癜之间的潜在联系。对于有严重血小板减少和微血管病性溶血迹象的患者,应进行必要的诊断检查,以排除与结核病并发血栓性血小板减少性紫癜的可能性。