Korean J Med.
1999 Feb;56(2):240-246.
A Case of Catastrophic Primary Antiphospholipid Syndrome
- Affiliations
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- 1Department of Internal Medicine, Pathology, School of Medicine, Catholic University of Taegu-Hyosung, Taegu, Korea.
- 2Department of Internal Medicine, Clinical Pathology, School of Medicine, Catholic University of Taegu-Hyosung, Taegu, Korea.
Abstract
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Catastrophic antiphospholipid syndrome is a rare clinical syndrome characterized by acute
multi-organ failure occurring in patients with antiphospholipid antibodies. It is associated
with involvement of several end-organs particularly kidneys, lungs, gastrointestinal tracts and
adrenal glands and presents catastrophic clinical pictures such as acute renal failure with
thrombotic microangiopathy, myocardial failure, adult respiratory distress syndrome, convulsion
and disseminated intravascular coagulation. Conventional treatments(e.g. intravenous heparin,
steroid, immunosuppressants) were not effective, while plasmapheresis seems to be a useful therapy.
We experienced a case of catastrophic primary antiphospholipid syndrome in 41-year-old woman
proved by renal biopsy and immuno-serological tests. She developed acute renal failure,
multiple esophageal and oral ulcers, adult respiratory distress syndrome, abnormal elevation of
hepatic and pancreatic enzymes and signs of disseminated intravascular coagulation. Evidences
of any other connective tissue diseases were not found. Renal biopsy revealed features of
thrombotic microangiopathic nephropathy and serum antiphospholipid antibody level was
elevated(34GPL). In spite of steroid, cyclophosphamide and supportive therapies, her
respiratory distress was not improved.