INFANTILE IDIOPATHIC THROMBOCYTOPENIC PURPURA

被引：9

作者：

BALLIN, A

KENET, G

TAMARY, H

RECHAVI, G

CHIVIDALLI, G

BURSTEIN, Y

TAUBER, T

NUSSINOVITCH, M

MEYTES, D

机构：

[1] DEPT PEDIAT, JERUSALEM, ISRAEL

[2] BEILINSON MED CTR, SAMBUR CTR PEDIAT HEMATOONCOL, PETAH TIQWA, ISRAEL

[3] SHEBA MED CTR, DEPT PEDIAT, RAMAT GAN, ISRAEL

[4] ICHILOV HOSP, TEL AVIV, ISRAEL

[5] ASSAF HAROFE MED CTR, ZERIFIN, ISRAEL

[6] HASHARON HOSP, ZERIFIN, ISRAEL

[7] SACKLER FAC MED, PETAM TIQWA, ISRAEL

[8] HADASSAH UNIV HOSP, IL-91120 JERUSALEM, ISRAEL

[9] EDITH WOLFSON MED CTR, DEPT PEDIAT, IL-85100 HOLON, ISRAEL

来源：

PEDIATRIC HEMATOLOGY AND ONCOLOGY | 1990年 / 7卷 / 04期

关键词：

Idiopathic thrombocytopenia purpura; Infant;

D O I：

10.3109/08880019009033409

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Idiopathic thrombocytopenic purpura (ITP) in childhood is a benign disease, as only 10% to 20% of (he patients have a chronic course. A retrospective study of 57 ITP patients ranging in age from four months to two years revealed that 30% of them proceeded to chronicity. Unlike ITP in the general pediatric population, chronic infantile ITP was characterized by male predominance, a high frequency of preceding viral infections, and lack of responsiveness to any of the known modalities of treatment. © 1990 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.

引用

页码：323 / 328

页数：6

共 13 条

[1] HIGH-DOSE INTRAVENOUS GAMMA-GLOBULIN THERAPY FOR NEONATAL AUTOIMMUNE THROMBOCYTOPENIA [J].