Iyori H, Bessho F, Ookawa H, Konishi S, Shirahata A, Miyazaki S, Fujisawa K, Akatsuka J
Division of Pediatrics, Kanagawa Prefectural Atsugi Hospital, Atsugi-City, Japan.
Ann Hematol. 2000 Dec;79(12):691-5. doi: 10.1007/s002770000219.
We sent questionnaires to hospitals in Japan in order to study the incidence and conditions of intracranial hemorrhage (ICH) in children with immune thrombocytopenic purpura (ITP). From 1980 to 1995, 11 cases of ICH were reported in eight patients with ITP at 35 institutions. One patient had ICH four times, but only one patient died of the condition. From 1990 through 1995, ICH occurred in four (0.52%) of 772 patients with ITP. None of the patients died. The platelet count when ICH occurred was 5.2 +/- 3.7 x 10(9)/l (mean +/- SD) (n = 11). Four of the eight patients (1980-1995) had received active treatment [e.g. intravenous immunoglobulin G (i.v. IgG)] immediately before ICH occurred. In seven cases (1980-1995), possible causes of ICH, including menstruation (n = 2) and viral infections (n = 3), were identified. Systemic lupus erythematosus (SLE) later developed in three patients. Although the incidence of ICH in children with ITP has not decreased compared with the rates in earlier studies, the mortality rate has decreased markedly. Our results suggest that menstruation, infection, and risk factors for progression to SLE may help to predict ICH in children with ITP. Large-scale prospective trials are needed to identify risk factors for ICH.
为研究免疫性血小板减少性紫癜(ITP)患儿颅内出血(ICH)的发生率及情况,我们向日本的医院发送了调查问卷。1980年至1995年期间,35家机构报告了8例ITP患儿发生11次ICH。1例患儿发生4次ICH,但仅1例死于该疾病。1990年至1995年期间,772例ITP患儿中有4例(0.52%)发生ICH。无一例患儿死亡。ICH发生时的血小板计数为5.2±3.7×10⁹/L(均值±标准差)(n = 11)。8例患儿中的4例(1980 - 1995年)在ICH发生前立即接受了积极治疗[如静脉注射免疫球蛋白G(i.v. IgG)]。1980年至1995年期间,在7例病例中确定了ICH的可能病因,包括月经(n = 2)和病毒感染(n = 3)。3例患儿后来发展为系统性红斑狼疮(SLE)。尽管与早期研究相比,ITP患儿ICH的发生率未降低,但死亡率已显著下降。我们的结果表明,月经、感染以及进展为SLE的危险因素可能有助于预测ITP患儿的ICH。需要进行大规模前瞻性试验以确定ICH的危险因素。