thrombophilia increases the incidence of pulmonary thrombosis significantly. various hereditary and acquired factors are known for thromboembolism. the hereditary factors are two common genetic autosomal mutations including factor v leidan mutation and prothrombin gene mutation. a descriptive- analytical design was conducted on 60 patients with thromboembolism who met the inclusion criteria. tw...

PURPOSE We retrospectively analyzed open pulmonary thromboembolectomy in patients with acute and chronic pulmonary thromboembolism. MATERIALS AND METHODS Between August 1990 and May 2005, 12 consecutive patients with acute and chronic pulmonary thromboembolism underwent open pulmonary thromboembolectomy at Yonsei Cardiovascular Center. Their mean age was 47.5 years, and 7 of the patients were...

Pulmonary embolism may be a life-threatening condition that needs immediate medical intervention. Early detection plays an important role in improving the survival rate. However, pulmonary embolism is a difficult diagnosis that may be missed because of non-specific clinical presentation. According to guidelines on the diagnosis and management of acute pulmonary embolism, it should be diagnosed ...

Hemoptysis is a crucial entity taking into account its morbidity and mortality. Pulmonary tuberculosis the leading cause for massive hemoptysis in our part of world, which if left untreated may be life threatening. We present case 37-year-old male patient with pulmonary concurrent thromboembolism presenting hemoptysis, was successfully managed Bronchial Artery Embolization. This represents that...

Venous thromboembolism, manifested as either deep venous thrombosis or pulmonary embolism (PE), is a major cause of morbidity and mortality in patients admitted to the intensive care unit. Clinically, PE may present as massive thromboembolism associated with cardiogenic shock or may be asymptomatic, as may occur with anatomically small emboli without hemodynamic or respiratory compromise. The m...