Guzel Tunccan Ozlem, Dizbay Murat, Senol Esin, Aki Zeynep, Ozdemir Kevser
Department of Clinical Microbiology and Infectious Diseases, Faculty of Medicine, Gazi University, Besevler, 06510 Ankara, Turkey.
Department of Hematology, Faculty of Medicine, Gazi University, Besevler, 06500 Ankara, Turkey.
Indian J Hematol Blood Transfus. 2014 Sep;30(Suppl 1):27-9. doi: 10.1007/s12288-012-0222-3. Epub 2013 Jan 10.
Mild anemia and leukopenia are the most common hematologic findings in the course of acute brucellosis. However severe form of thrombocytopenia is less frequently reported. The patient was admitted to the hospital with fever, gingival bleeding, and petechial skin lesions related to severe thrombocytopenia. He was investigated for the causes of thrombocytopenia. Test results showed that Wright agglutination test was positive at 1/5120 titer, and blood culture was positive for Brucella melitensis. Finally, he was diagnosed as acute brucellosis. Rifampicin and doxycycline treatment was started on he third day of admission. A bone marrow aspiration was performed on the seventh day of admission because of severe thrombocytopenia did not response to brucellosis treatment. The result of bone marrow aspiration was consistent with idiopathic thrombocytopenic purpura. With the addition of corticosteroid treatment, his complaints resolved immediately, and thrombocyte count rose to normal range. He was discharged on the 12th day of rifampicin and doxycycline therapy, and he was successfully completed 6-week therapy. In cases of brucella induced immune thrombocytopenia, corticosteroid treatment might be useful for the prevention of bleeding complications.
轻度贫血和白细胞减少是急性布鲁氏菌病病程中最常见的血液学表现。然而,严重形式的血小板减少症报道较少。该患者因发热、牙龈出血和与严重血小板减少相关的皮肤瘀点入院。对其血小板减少的原因进行了调查。检测结果显示,wright凝集试验滴度为1/5120呈阳性,血培养羊种布鲁氏菌呈阳性。最终,他被诊断为急性布鲁氏菌病。入院第三天开始使用利福平及强力霉素治疗。由于严重血小板减少对布鲁氏菌病治疗无反应,入院第七天进行了骨髓穿刺。骨髓穿刺结果与特发性血小板减少性紫癜相符。加用皮质类固醇治疗后,他的症状立即缓解,血小板计数升至正常范围。利福平及强力霉素治疗第12天他出院,并成功完成了6周的治疗。在布鲁氏菌引起的免疫性血小板减少症病例中,皮质类固醇治疗可能有助于预防出血并发症。