Splenic infarct, atypical presentation of babesiosis: A case report

Q4 Medicine
Radiology Case Reports Pub Date : 2026-04-01 Epub Date: 2026-02-02 DOI:10.1016/j.radcr.2026.01.016
Zinaida Perciuleac MD , Melissa R. George DO , Maya P. Fares MD , Rezhan Hussein MD
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引用次数: 0

Abstract

Babesiosis is a tick-borne protozoan infection marked by invasion of red blood cells and causing hemolytic anemia. When symptomatic, patients present with symptoms and signs secondary to hemolysis. We report a case of Babesiosis presenting with a rare manifestation of a splenic infarct, emphasizing the importance of early recognition and prompt treatment. A 41-year-old man with no significant past medical history presented to the hospital with fever, chills and sweats for 2 days. He also had left lower quadrant abdominal pain which started 10 days prior to the admission. Initial laboratory results showed mild anemia and thrombocytopenia with a platelet count of 79 K/uL (normal range 150-350), normal creatinine and transaminases. Computerized tomography (CT) of the abdomen showed moderate splenomegaly and 1.2 cm hyperdense focus reflecting an infarct. Peripheral blood smear demonstrated intracellular red cell inclusions suggestive of Babesia spp. Human Babesiosis is an emerging zoonosis with various clinical presentations varying from being asymptomatic to life-threatening conditions. Patients with immunocompromised status, splenectomy, or significant underlying health conditions are particularly susceptible to severe manifestations. Splenic infarcts are reported as a rare complication, found in younger and immunocompetent hosts, and they do not correlate with the level of parasitemia. Our patient was also a young immunocompetent host with a low level of parasitemia presented with abdominal pain; a high level of suspicion is needed to make an early diagnosis. This case is an important reminder of this atypical presentation of Babesia microti infection in an immunocompetent host.

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不典型巴贝斯虫病表现的脾梗死1例。
巴贝斯虫病是一种蜱传播的原生动物感染,其特征是侵入红细胞并引起溶血性贫血。有症状时,患者表现出溶血的继发症状和体征。我们报告一例巴贝斯虫病表现为罕见的脾梗死,强调早期识别和及时治疗的重要性。41岁男性,无明显既往病史,因发热、发冷、出汗2天就诊。入院前10天开始出现左下腹疼痛。最初的实验室结果显示轻度贫血和血小板减少,血小板计数79 K/uL(正常范围150-350),肌酐和转氨酶正常。腹部CT显示中度脾肿大,1.2 cm高密度灶反映梗死。人巴贝斯虫病是一种新出现的人畜共患病,临床表现从无症状到危及生命不等。免疫功能低下、脾切除或有重大潜在健康状况的患者特别容易出现严重症状。脾梗死是一种罕见的并发症,在年轻和免疫能力强的宿主中发现,它们与寄生虫血症水平无关。我们的患者也是一个年轻的免疫能力强的宿主,低水平的寄生虫血症表现为腹痛;早期诊断需要高度的怀疑。这个病例是一个重要的提醒,这种非典型的巴贝斯虫感染在免疫能力强的宿主。
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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来源期刊
Radiology Case Reports
Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.10
自引率
0.00%
发文量
1074
审稿时长
30 days
期刊介绍: The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.
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