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A case of primary antiphospholipid syndrome with pulmonary thromboembolism

Title
A case of primary antiphospholipid syndrome with pulmonary thromboembolism
Authors
Jae B.L.Yun S.S.Young W.N.Hye S.P.Chung H.T.So Y.L.Yoon H.J.Yon J.R.Eun M.C.Jin H.L.Jung H.C.Jin W.M.
Ewha Authors
장중현이진화천은미류연주
SCOPUS Author ID
장중현scopus; 이진화scopusscopus; 천은미scopus; 류연주scopus
Issue Date
2007
Journal Title
Tuberculosis and Respiratory Diseases
ISSN
1738-3536JCR Link
Citation
Tuberculosis and Respiratory Diseases vol. 63, no. 1, pp. 72 - 77
Indexed
SCOPUS; KCI scopus
Document Type
Article
Abstract
Antiphospholipid syndrome (APS) causes recurrent thromboses and morbidity during pregnancy, including fetal loss. This malady is associated with the persistent presence of anticardiolipin antibody or lupus anticoagulant. The pulmonary manifestations of antiphospholipid syndrome include pulmonary thromboembolism, pulmonary hypertension, acute respiratory distress syndrome, etc. Pulmonary thromboembolism is often the initial manifestation of antiphospholipid syndrome and a timely diagnosis is critical due to the high mortality rate. We herein report on a 19-year-old man with pulmonary thromboembolism that was caused by primary antiphospholipid syndrome. He presented with blood-tinged sputum, fever and epigastric pain, and his chest computerized tomography showed pulmonary thromboembolism. The other possible causes of pulmonary thromboembolism were excluded and the diagnosis of primary antiphospholipid syndrome was confirmed by the lupus anticoagulant that was present on two occasions six weeks apart. We also discuss the nature and management of antiphospholipid syndrome, along with a brief review of the relevant literatures.
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의과대학 > 의학과 > Journal papers
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