Severe Thrombocytopenia Secondary to Babesiosis: A Case Report

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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Publication Details

Journal
Case Reports in Hematology
Published
2025-01-01
DOI
https://doi.org/10.1155/crh/9918329
Primary Topic
Platelet Disorders and Treatments
Type
article
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0.00
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article

Severe Thrombocytopenia Secondary to Babesiosis: A Case Report

Sharath Kommu, Vidyasagar Cirra, Michael Husak, Christopher Osterbauer
Case Reports in Hematology
Platelet Disorders and Treatments
article

Severe Thrombocytopenia Secondary to Babesiosis: A Case Report

Sharath Kommu, Vidyasagar Cirra, Michael Husak, Christopher Osterbauer
article en

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.

Case Reports in HematologyVol. 2025(1)
Marshfield Clinic (US), Marshfield Clinic (US)
Good health and well-being
Openalex Percentile: Top 80%
Platelet Disorders and Treatments
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Severe Thrombocytopenia Secondary to Babesiosis: A Case Report — Sharath Kommu, Vidyasagar Cirra, et al. · Case Reports in Hematology (2025) | TGRS Research Map | TGRS