The Carman and Ann Adams Department of Pediatrics, Pediatric Hematology/Oncology Division, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan, USA.
Pediatr Blood Cancer. 2010 Sep;55(3):508-11. doi: 10.1002/pbc.22570.
Acute immune thrombocytopenic purpura (ITP) is a common, benign, self-limiting disease in children. Chronic ITP is diagnosed when thorombocytopenia persists beyond 12 months. Older age is associated with increased risk for development of chronic ITP. The main objective of the current study was to examine whether total leukocyte (TLC) and absolute lymphocyte counts (ALC) at diagnosis correlate with the persistence of ITP beyond 6 months.
Two hundred and twenty four consecutive medical records for patients diagnosed with immune thrombocytopenia, between April 1993 and July 2007, were reviewed and 188 patients were eligible for analysis. Case records were examined to ascertain the following information: age, gender, ethnicity, date of presentation, presenting CBC with differential count, treatment given and the outcome.
The male to female ratio was almost 1:1; 24% (45/188) of patients had persistent ITP beyond 6 months. We determined that age >8.5 year, TLC < 6,250/microl and ALC < 3,050/microl was associated with a significant risk for development of persistent ITP beyond 6 months.
TLC and ALC at diagnosis are predictive variables for the development of persistent/chronic ITP. Further studies are recommended to confirm the current finding and to assess the underlying pathophysiology with the course of the ITP.
急性免疫性血小板减少性紫癜(ITP)是儿童中常见的良性、自限性疾病。当血小板减少持续超过 12 个月时,就会诊断为慢性 ITP。年龄较大与慢性 ITP 发展的风险增加有关。本研究的主要目的是研究诊断时的总白细胞(TLC)和绝对淋巴细胞计数(ALC)是否与 ITP 持续超过 6 个月有关。
回顾了 1993 年 4 月至 2007 年 7 月期间诊断为免疫性血小板减少症的 224 例连续病历,其中 188 例符合分析条件。检查病历以确定以下信息:年龄、性别、种族、就诊日期、就诊时的全血细胞计数和分类计数、给予的治疗和结果。
男女比例几乎为 1:1;24%(45/188)的患者 ITP 持续超过 6 个月。我们发现年龄>8.5 岁、TLC<6,250/µl 和 ALC<3,050/µl 与 ITP 持续超过 6 个月的显著风险相关。
诊断时的 TLC 和 ALC 是预测 ITP 持续/慢性发展的变量。建议进一步研究以确认目前的发现,并评估 ITP 病程中的潜在病理生理学。