Mak Y K, Yu P H, Chan C H, Chu Y C
Department of Medicine, Queen Elizabeth Hospital, Hong Kong, China.
Clin Lab Haematol. 2000 Dec;22(6):355-8. doi: 10.1046/j.1365-2257.2000.00340.x.
We performed a retrospective analysis of bone marrow examination (BME) in the management of Chinese adult patients less than 60 years of age with isolated thrombocytopenia at presentation. Eighty-three patients with a median age of 39 years presenting with isolated thrombocytopenia (median platelet count: 38 x 10(9)/l) had routinely undergone BME as part of the laboratory investigations during the period from January 1996 to December 1999. All 83 patients had bone marrow findings of active marrow suggesting causes due to peripheral destruction. All of these patients responded to steroid or intravenous immunoglobulin (IVIg) therapy at presentation if their platelet counts were significantly low or if they had mucosal bleeding. Eighty-one of the 83 patients, after a median of 20 months follow-up, were finally diagnosed as having idiopathic thrombocytopenic purpura (ITP). The remaining two patients were finally confirmed as cases of systemic lupus erythematosus (SLE). Our results suggest that BME is not helpful in the diagnosis of isolated thrombocytopenia or suspected ITP in adult patients at presentation, provided that a thorough clinical history and physical examination are undertaken and that the blood count and peripheral blood smear show no abnormalities apart from the thrombocytopenia.
我们对1996年1月至1999年12月期间年龄小于60岁、初诊时表现为单纯血小板减少的中国成年患者进行了骨髓检查(BME)的回顾性分析。83例中位年龄为39岁、表现为单纯血小板减少(中位血小板计数:38×10⁹/L)的患者在实验室检查期间常规接受了BME。所有83例患者的骨髓检查结果均显示骨髓活跃,提示病因是外周破坏。如果这些患者的血小板计数显著降低或有黏膜出血,他们在初诊时对类固醇或静脉注射免疫球蛋白(IVIg)治疗均有反应。83例患者中的81例,经过中位20个月的随访,最终被诊断为特发性血小板减少性紫癜(ITP)。其余2例患者最终被确诊为系统性红斑狼疮(SLE)。我们的结果表明,如果进行了全面的临床病史采集和体格检查,且血细胞计数和外周血涂片除血小板减少外无异常,那么BME对初诊时成年患者的单纯血小板减少或疑似ITP的诊断并无帮助。