Lagler Heimo, Matt Ulrich, Sillaber Christian, Winkler Stefan, Graninger Wolfgang
Department of Internal Medicine I, Division of Infectious Diseases and Chemotherapy, Medical University of Vienna, Austria.
Acta Biomed. 2006;77 Suppl 2:22-5.
We report a case of a 26-year-old female from Kenya who suffered from intermittent fever of unknown origin for one month. The major findings on admission were pancytopenia associated with considerable splenomegaly. The diagnosis was established by visualisation of amastigotes in bone marrow biopsy and by detection of antibodies to Leishmania spp. in blood. The infection was treated intravenously with liposomal amphotericin B for five days. The patient was afebrile after the first infusion. No relapse was reported.
我们报告一例来自肯尼亚的26岁女性病例,该患者持续一个月不明原因间歇性发热。入院时主要检查结果为全血细胞减少伴明显脾肿大。通过骨髓活检中无鞭毛体的可视化以及血液中利什曼原虫属抗体的检测确诊。感染采用脂质体两性霉素B静脉治疗五天。首次输注后患者不再发热。未报告复发情况。