Is there a microangiopathic antiphospholipid syndrome?

被引：30

作者：

Asherson, Ronald A. ^{[1
]}

Pierangeli, Sylvia S.

Cervera, Ricard

机构：

[1] Univ Witwatersrand, Div Immunol, Sch Pathol, ZA-2196 Johannesburg, South Africa

[2] Univ Texas, Div Rheumatol, Galveston, TX 77555 USA

[3] Hosp Clin Barcelona, Dept Autoimmune Dis, Barcelona, Catolonia, Spain

来源：

ANNALS OF THE RHEUMATIC DISEASES | 2007年 / 66卷 / 04期

关键词：

THROMBOTIC THROMBOCYTOPENIC PURPURA; SYSTEMIC-LUPUS-ERYTHEMATOSUS; HEMOLYTIC-UREMIC SYNDROME; DISSEMINATED INTRAVASCULAR COAGULATION; SUBUNGUAL SPLINTER HEMORRHAGES; REFRACTORY HELLP-SYNDROME; CELL-ADHESION MOLECULE-1; VON-WILLEBRAND-FACTOR; ENDOTHELIAL-CELLS; TISSUE FACTOR;

D O I：

10.1136/ard.2006.067033

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Revealing the evolution of the term APS and its commonalities with other microangiopathic disorders.

引用

页码：429 / 432

页数：4

共 89 条

[1] Preeclampsia and liver infarction in early pregnancy associated with the antiphospholipid syndrome [J].

Alsulyman, OM ;

Castro, MA ;

Zuckerman, E ;

McGehee, W ;

Goodwin, TM .

OBSTETRICS AND GYNECOLOGY, 1996, 88 (04) :644-646

[2] The role of the tissue factor pathway in the hypercoagulable state in patients with the antiphospholipid syndrome [J].

Amengual, O ;

Atsumi, T ;

Khamashta, MA ;

Hughes, GRV .

THROMBOSIS AND HAEMOSTASIS, 1998, 79 (02) :276-281

[3] Thrombotic thrombocytopenic purpura with severe ADAMTS-13 deficiency in two patients with primary antiphospholipid syndrome [J].

Amoura, Z ;

Costedoat-Chalumeau, N ;

Veyradier, AS ;

Wolf, M ;

Ghillani-Dalbin, P ;

Cacoub, P ;

Meyer, D ;

Piette, JC .

ARTHRITIS AND RHEUMATISM, 2004, 50 (10) :3260-3264

[4] Anticardiolipin antibodies in classic pediatric hemolytic-uremic syndrome:: A possible pathogenic role [J].

Ardiles, LG ;

Olavarría, F ;

Elgueta, M ;

Moya, P ;

Mezzano, S .

NEPHRON, 1998, 78 (03) :278-283

[5]

Asherson R.A., 2006, FUTURE RHEUMATOL, V1, P355, DOI [10.2217/17460816.1.3.355, DOI 10.2217/17460816.1.3.355]

[6] SUBUNGUAL SPLINTER HEMORRHAGES - A NEW SIGN OF THE ANTIPHOSPHOLIPID COAGULOPATHY [J].

ASHERSON, RA .

ANNALS OF THE RHEUMATIC DISEASES, 1990, 49 (04) :268-268

[7] THE PRIMARY ANTIPHOSPHOLIPID SYNDROME - MAJOR CLINICAL AND SEROLOGICAL FEATURES [J].

ASHERSON, RA ;

KHAMASHTA, MA ;

ORDIROS, J ;

DERKSEN, RHWM ;

MACHIN, SJ ;

BARQUINERO, J ;

OUTT, HH ;

HARRIS, EN ;

VILARDELLTORRES, M ;

HUGHES, GRV .

MEDICINE, 1989, 68 (06) :366-374

[8] Catastrophic antiphospholipid syndrome -: Clinical and laboratory features of 50 patients [J].

Asherson, RA ;

Cervera, R ;

Piette, JC ;

Font, J ;

Lie, JT ;

Burcoglu, A ;

Lim, K ;

Muñoz-Rodríguez, FJ ;

Levy, RA ;

Boué, F ;

Rossert, J ;

Ingelmo, M .

MEDICINE, 1998, 77 (03) :195-207

[9] Multiorgan failure and antiphospholipid antibodies: the catastrophic antiphospholipid (Asherson's) syndrome [J].

Asherson, RA .

IMMUNOBIOLOGY, 2005, 210 (10) :727-733

[10] Disseminated intravascular coagulation in catastrophic antiphospholipid syndrome:: clinical and haematological characteristics of 23 patients [J].

Asherson, RA ;

Espinosa, G ;

Cervera, R ;

Gómez-Puerta, JA ;

Musuruana, J ;

Bucciarelli, S ;

Ramos-Casal, M ;

Martínez-González, AL ;

Ingelmo, M ;

Reverter, JC ;

Font, J ;

Triplett, DA .

ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 (06) :943-946

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