THROMBOTIC THROMBOCYTOPENIC PURPURA ASSOCIATED WITH SICKLE CELL-HEMOGLOBIN-C-DISEASE

被引：15

作者：

CHINOWSKY, MS

机构：

[1] Department of Internal Medicine, Kaiser Permanente Medical Center, Harbor, CA

来源：

SOUTHERN MEDICAL JOURNAL | 1994年 / 87卷 / 11期

关键词：

D O I：

10.1097/00007611-199411000-00025

中图分类号：

R5 [内科学];

学科分类号：

1002 [临床医学]; 100201 [内科学];

摘要：

Thrombotic thrombocytopenic purpura (TTP) complicated a vaso-occlusive crisis in a patient with sickle cell-hemoglobin C (HbSC) disease. Markedly abnormal HbSC red blood cell morphology confused the initial diagnostic evaluation of the peripheral smear. Sustained, severe thrombocytopenia and the patient's failure to respond clinically to RBC exchange transfusion helped to indicate the proper diagnosis that led to effective therapy.

引用

页码：1168 / 1171

页数：4

共 38 条

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SEVERE THROMBOCYTOPENIA IN SICKLE-CELL CRISIS [J].