PRIMARY ANTIPHOSPHOLIPID SYNDROME AND EVAN'S SYNDROME: 2 CASE REPORTS

被引：0

作者：

Khalifa, M. ^{[1
]}

Ghannouchi, N. ^{[1
]}

Kaabia, N. ^{[1
]}

Benjazia, E. ^{[1
]}

Hachfi, W. ^{[1
]}

Krifa, A. ^{[1
]}

Letaief, A. ^{[1
]}

Bahri, F. ^{[1
]}

机构：

[1] Univ Hosp F Hached, Dept Internal Med & Infect Dis, Sousse 4000, Tunisia

来源：

ACTA CLINICA BELGICA | 2009年 / 64卷 / 01期

关键词：

primary antiphospholipid syndrome; antiphospholid antibodies; Evan's syndrome; thrombocytopaenia; autoimmune haemolytic anaemia; SYSTEMIC LUPUS-ERYTHEMATOSUS; THROMBOCYTOPENIA;

D O I：

10.1179/acb.2009.012

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The main clinical features of primary antiphospholipid syndrome are recurrent foetal toss, arterial or venous thrombosis and thrombocytopaenia. Evan's syndrome is characterized by simultaneous or sequential association of autoimmune anaemia and thombocytopaenia, rarely reported in primary antiphospholipid syndrome. We describe 2 cases of this association. Treatment with steroids was started in both cases, the follow-up was marked by the normalization of haemoglobin value and platelet count, without relapse.

引用

页码：65 / 67

页数：3

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