Peer-reviewed veterinary case report
Dog with severe Babesia vulpes infection treated after spleen removal
By Fernández, Yordan et al.·Published in Topics in companion animal medicine·2025·AniCura Imavet Referencia Veterinaria, Spain·View original on PubMed →
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Original publication title: Successful treatment of a dog with a severe Babesia vulpes infection and associated haemophagocytic syndrome after splenectomy.
- Species:
- dog
Plain-English summary
A 12-year-old female crossbreed dog was brought in with severe anemia and a high fever after being diagnosed with a Babesia vulpes infection, which is a type of blood parasite. Despite initial treatments, including blood transfusions and medications, her condition worsened, leading to a referral for specialized care. After further testing, she was diagnosed with a serious complication called haemophagocytic syndrome, where her immune system was attacking her own blood cells. The dog received a combination of immunosuppressive therapy and additional blood transfusions, which helped her recover. After ten days, her anemia improved, and follow-up tests showed no signs of the infection.
People also search for: dog Babesia infection treatment · crossbreed dog anemia · splenectomy complications in dogs
Abstract
A 12-year-old female, neutered, crossbreed dog was diagnosed by its primary care practice with severe Babesia vulpes infection, based on positive PCR testing, three weeks after elective splenectomy for splenic nodules identified on abdominal ultrasound. Despite treatment with standard antiprotozoal therapy, glucocorticoids, and three blood transfusions, anaemia persisted, becoming non-regenerative and prompting referral. Upon presentation, the dog exhibited pale mucous membranes and was hyperthermic. Blood tests revealed a regenerative anaemia, thrombocytopenia, hyperbilirubinaemia, hypertriglyceridaemia, hyperferritinaemia and elevated liver enzyme activity. Coombs' testing was negative, and thoracic and abdominal imaging were unremarkable. A repeated Babesia vulpes PCR was positive and screening for other infectious diseases was negative. Bone marrow cytology and histopathology showed generalised hyperplasia, with macrophages comprising ≥3% of the total nucleated cells. These macrophages displayed prominent erythrophagia and, to a lesser extent, engulfment of mature neutrophils, platelets, and nucleated red blood cells. Therefore, a diagnosis of haemophagocytic syndrome associated with a severe Babesia vulpes infection was made. The dog received double immunosuppressive therapy, a combination of antiprotozoal drugs and a further three blood transfusions. The thrombocytopenia quickly resolved, with the anaemia improving ten days later. The antiprotozoal and immunosuppressive therapies were eventually discontinued without relapse of the babesiosis and repeated Babesia vulpes PCR testing was negative. To the authors' knowledge, this is the first report to describe the successful treatment of a splenectomised dog with severe Babesia vulpes infection complicated by haemophagocytic syndrome.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/41274494/