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Tuberculosis-associated Immune Thrombocytopenia: A Case Report

机译:结核相关的免疫性血小板减少症:一例报告

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摘要

Various hematological manifestations are known to occur with tuberculosis (TB), but its association with immune thrombocytopenia is uncommon and not well recognized. Here, the case of a 39-year-old male who presented with a history of epistaxis and hematuria is described. The patient was found to have diffuse lymphadenopathy both clinically and radiologically. He was diagnosed with immune thrombocytopenia; however, there was a delay in the diagnosis of TB because of the patient's refusal of lymph node biopsy and late recognition of the association between TB and immune thrombocytopenia. Treatment with steroids without antituberculosis medications may have led to reactivation and dissemination of tuberculous infection in this patient. Later, the patient was readmitted with a suspected community-acquired pneumonia and the sputum smear was positive for acid-fast bacilli. Unfortunately, the patient died after he developed sepsis and multiorgan failure. The purpose of this case report is to highlight this rare combination and create awareness among clinicians to consider TB as an underlying etiology of immune thrombocytopenia, especially if there are other associated physical findings such as the presence of lymphadenopathy.
机译:已知结核(TB)会发生多种血液学表现,但其与免疫性血小板减少症的关联并不常见,也未得到很好的认识。在此,描述了具有鼻出血和血尿病史的39岁男性病例。发现该患者在临床和放射学上均患有弥漫性淋巴结病。他被诊断出患有免疫性血小板减少症;然而,由于患者拒绝进行淋巴结活检以及对结核与免疫性血小板减少症之间联系的较晚认识,导致结核病的诊断延迟。不使用抗结核药物的类固醇治疗可能导致该患者的结核感染重新活化和传播。后来,该患者因怀疑是社区获得性肺炎而再次入院,并且痰涂片中的抗酸杆菌属呈阳性。不幸的是,患者在出现败血症和多器官衰竭后死亡。本病例报告的目的是强调这种罕见的组合,并在临床医生中引起人们的认识,将结核病视为免疫性血小板减少的根本病因,尤其是在存在其他相关物理发现(例如淋巴结病的存在)的情况下。

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