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儿童特发性血小板减少症。爱丁堡1962 - 1982年的经验

Idiopathic thrombocytopenia in childhood. Edinburgh experience 1962-82.

作者信息

Hoyle C, Darbyshire P, Eden O B

出版信息

Scott Med J. 1986 Jul;31(3):174-9.

PMID:3798080
Abstract

This retrospective review of 136 children with idiopathic thrombocytopenia assesses the prognostic significance of various presenting parameters and the effect of therapy. Initial haemoglobin, white cell count, actual platelet count, splenomegaly, hepatomegaly and lymphadenopathy had no significant effect upon the final outcome. Cases of acute I.T.P. were associated with a higher incidence of preceding infection, a shorter history of bleeding and a preponderance of males. The presence of greater than 20 per cent lymphocytes in the bone marrow was associated with a longer time to achieve a normal platelet count (p = 0.05). Steroid therapy shortened the time for acute cases of I.T.P. to obtain a normal platelet count (p = 0.05), but had no effect on long-term prognosis. Chronicity occurred in 25 children (18%) and nine of these had spontaneous remissions. Immunosuppressive therapy was ineffective, but nine out of 12 children were cured by splenectomy. Mortality was 0.7 per cent (one death) and general morbidity was low.

摘要

这项对136例特发性血小板减少症患儿的回顾性研究评估了各种临床表现参数的预后意义及治疗效果。初始血红蛋白、白细胞计数、实际血小板计数、脾肿大、肝肿大及淋巴结病对最终结局无显著影响。急性特发性血小板减少性紫癜(ITP)病例与先前感染发生率较高、出血病史较短及男性居多有关。骨髓中淋巴细胞比例大于20%与血小板计数恢复正常所需时间较长相关(p = 0.05)。类固醇治疗缩短了急性ITP病例血小板计数恢复正常的时间(p = 0.05),但对长期预后无影响。25例患儿(18%)转为慢性,其中9例自发缓解。免疫抑制治疗无效,但12例患儿中有9例通过脾切除术治愈。死亡率为0.7%(1例死亡),总体发病率较低。

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