Acquired haemophilia A: errors in the diagnosis

被引:27
作者
Kazmi, MA [1 ]
Pickering, W [1 ]
Smith, MP [1 ]
Holland, LJ [1 ]
Savidge, GF [1 ]
机构
[1] St Thomas Hosp, Reference Ctr Haemostat & Thrombot Disorders, London SE1 7EH, England
关键词
inhibitor; antiphospholipid antibodies; acquired haemophilia; systemic lupus erythematosus;
D O I
10.1097/00001721-199810000-00009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The distinction between a specific factor inactivator and a non-specific inhibitor is important when confronted by a patient with a history of bleeding and abnormal in-vitro coagulation tests. We report on two patients who presented with bleeding and a prolonged activated partial thromboplastin time. Initial factor assays suggested combined deficiency of factors VIII and IX as a result of the presence of inactivators. The use of dilution studies, chromogenic assays, a novel in-house enzyme-linked-immunosorbent-assay-based technique and phospholipid neutralization, demonstrated that Case 1 had a genuine factor VIII inactivator resulting in factor VIII levels of less than 1 IU/dl but no factor IX deficiency. Case 2 had normal levels of factor VIII on further testing and no specific inactivator to either factor VIII or IX but a potent antiphospholipid antibody which had interfered with the phospholipid-dependent in-vitro assays. Care must be taken in the interpretation of laboratory assays in the presence of antiphospholipid antibodies to ensure that the correct diagnosis is made and inappropriate treatment avoided. (C) 1998 Lippincott Williams & Wilkins.
引用
收藏
页码:623 / 628
页数:6
相关论文
共 12 条
[1]   An approach to factor assays in patients with strong lupus anticoagulants [J].
Armitage, J ;
Ashcraft, J ;
Kim, A ;
Kaplan, HS .
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 1995, 1 (02) :125-130
[2]  
BALLARD HS, 1993, BRIT J RHEUMATOL, V32, P515
[3]   COAGULATION DEFECTS IN A CASE OF SYSTEMIC LUPUS ERYTHEMATOSUS WITH THROMBOCYTOPENIA [J].
BONNIN, JA ;
COHEN, AK ;
HICKS, ND .
BRITISH JOURNAL OF HAEMATOLOGY, 1956, 2 (02) :168-179
[4]   INCOAGULABILITY OF BLOOD IN SYSTEMIC-LUPUS-ERYTHEMATOSUS - A CASE DUE TO HYPOPROTHROMBINEMIA AND A CIRCULATING ANTICOAGULANT [J].
CORRIGAN, JJ ;
PATTERSON, JH ;
MAY, NE .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1970, 119 (04) :365-+
[5]  
GREEN D, 1981, THROMB HAEMOSTASIS, V45, P200
[6]   THE 2ND INTERNATIONAL ANTICARDIOLIPIN STANDARDIZATION WORKSHOP THE KINGSTON ANTIPHOSPHOLIPID ANTIBODY STUDY (KAPS) GROUP [J].
HARRIS, EN .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1990, 94 (04) :476-484
[7]  
KASPER CK, 1975, THROMB DIATH HAEMOST, V34, P869
[8]  
KASPER CK, 1995, ACQUIRED HAEMOPHILIA, P9
[9]   ACQUIRED HEMOPHILIA - A NATURAL-HISTORY STUDY OF 16 PATIENTS WITH FACTOR-VIII INHIBITORS RECEIVING LITTLE OR NO THERAPY [J].
LOTTENBERG, R ;
KENTRO, TB ;
KITCHENS, CS .
ARCHIVES OF INTERNAL MEDICINE, 1987, 147 (06) :1077-1081
[10]   PLASMA COAGULATION DEFECT IN SYSTEMIC LUPUS ERYTHEMATOSUS ARISING FROM HYPOPROTHROMBINEMIA COMBINED WITH ANTIPROTHROMBINASE ACTIVITY [J].
RAPAPORT, SI ;
AMES, SB ;
DUVALL, BJ .
BLOOD, 1960, 15 (02) :212-227