Pamuk Gulsum Emel, Dogan Celik Aygul, Uyanik Mehmet Sevki
Division of Hematology, Trakya University Medical Faculty, Edirne, Turkey.
Med Princ Pract. 2009;18(4):329-31. doi: 10.1159/000215733. Epub 2009 Jun 2.
To present a case of acute brucellosis triggering acute hemolytic anemia in a subject with glucose-6-phosphate dehydrogenase (G6PD) deficiency.
A 17-year-old male patient presented with fever, malaise and jaundice. His blood and bone marrow cultures yielded Brucella species. In addition, he was found to have acute hemolytic anemia due to previously undiagnosed G6PD deficiency. He was started on folic acid supplementation and given a combination of doxycycline and rifampicin for 6 weeks. His response to antibiotic therapy was optimal; the hemolytic anemia resolved. There were no further episodes of hemolysis.
This case showed that the differential diagnosis of acute hemolytic anemia in subjects with G6PD deficiency should include brucellosis, especially in regions where the infection is endemic.
报告1例葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症患者因急性布鲁氏菌病引发急性溶血性贫血的病例。
一名17岁男性患者出现发热、乏力和黄疸。其血液和骨髓培养分离出布鲁氏菌属。此外,发现他因先前未诊断出的G6PD缺乏症而患有急性溶血性贫血。开始给他补充叶酸,并给予多西环素和利福平联合治疗6周。他对抗生素治疗反应良好;溶血性贫血得到缓解。未再发生溶血。
该病例表明,G6PD缺乏症患者急性溶血性贫血的鉴别诊断应包括布鲁氏菌病,尤其是在该感染流行的地区。