Severe Thrombocytopenia Secondary to Babesiosis: A Case Report.

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2025-07-01 eCollection Date: 2025-01-01 DOI:10.1155/crh/9918329
Vidyasagar R Cirra, Sharath Kommu, Michael Husak, Christopher Osterbauer
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Abstract

A 76-year-old man with a history of atrial fibrillation treated with warfarin, renal calculi with a history of lithotripsy, hypertension, anxiety, and diabetes mellitus with recent tick exposure presented with abdominal pain, fatigue, nausea, and fever with chills. Workup revealed thrombocytopenia and hemolysis. Due to the likelihood of immune thrombocytopenia (ITP) secondary to a viral etiology, the patient was initially started on steroids. The patient subsequently tested positive for babesiosis on peripheral smear and polymerase chain reaction. A peripheral smear showed giant platelets and was positive for immunoglobulin M platelet antibodies. Other etiologies of thrombocytopenia were excluded. The patient was diagnosed with ITP secondary to babesiosis. Antibiotics were initiated to treat babesiosis. The platelet count was nonresponsive to steroids and gradually improved following intravenous immunoglobulin administration and continued antibiotic treatment. This rare case highlights the importance of considering ITP secondary to babesiosis as the etiology of severe thrombocytopenia in babesiosis, as appropriate recognition and early treatment of babesiosis and ITP can prevent serious complications.

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巴贝斯虫病继发严重血小板减少1例。
76岁男性,心房颤动史,华法林治疗,肾结石,有碎石史,高血压,焦虑,糖尿病,近期接触蜱虫,表现为腹痛,疲劳,恶心,发热伴寒战。检查发现血小板减少和溶血。由于继发于病毒性病因的免疫性血小板减少症(ITP)的可能性,患者最初开始使用类固醇。患者随后外周血涂片和聚合酶链反应检测为巴贝斯虫病阳性。外周涂片显示巨大血小板,免疫球蛋白M血小板抗体阳性。排除了血小板减少症的其他病因。患者被诊断为继发于巴贝斯虫病的ITP。开始使用抗生素治疗巴贝斯虫病。血小板计数对类固醇无反应,在静脉注射免疫球蛋白和持续抗生素治疗后逐渐改善。这一罕见病例强调了将继发于巴贝斯虫病的ITP视为巴贝斯虫病中严重血小板减少的病因的重要性,因为适当的识别和早期治疗巴贝斯虫病和ITP可以预防严重的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
13 weeks
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