نتایج جستجو برای: chylopericardium

تعداد نتایج: 149  

Journal: :The Journal of Thoracic and Cardiovascular Surgery 1981

Journal: :American Journal of Roentgenology 1977

Journal: :Nihon Naika Gakkai Zasshi 1976

Journal: :The Journal of Thoracic and Cardiovascular Surgery 1984

Journal: :Interactive cardiovascular and thoracic surgery 2002
Ghassan Sleilaty Issam Rassi Abdallah Alawi Victor A Jebara

Primary isolated chylopericardium is a rare entity. Its exact pathophysiology is still unknown. A case of chronic isolated primary pericardium diagnosed 12 years after the initial diagnosis of an asymptomatic pericardial effusion is reported. The diagnosis was established incidentally during surgery for resection of a papillary fibroelastoma of the aortic valve.

Journal: :The Journal of Thoracic and Cardiovascular Surgery 1971

Journal: :Circulation 1959
D C CONNOLLY T J DRY A C GOOD O CLAGETT H B BURCHELL

Persistent pericardial effusion in the absence of obvious preceding or concurrent disease presents a baffling problem. In such cases chylopericardium, cholesterol pericarditis, lupus erythematosus, malignant disease, myxedema, severe anemia, and scleroderma, must be considered. Six cases are reported with large effusions present for from 1 to 11 years. The diagnostic measures to be used, the re...

Journal: :Revista espanola de cardiologia 2007
Jorge L Cervantes-Salazar Juan E Calderón-Colmenero Samuel Ramírez-Marroquín

1. Kobayashi Y, Amaro M, Fitzgerald PJ. Acute coronary closure after stenting: a lesson from intravascular ultrasound. Int J Cardiovasc Intervent. 1999;2:51-4. 2. Murasato Y, Suzuka H, Suzuki Y. Incomplete stent apposition in a left main bifurcated lesion after kissing stent implantation. J Invasive Cardiol. 2006;18:E279-84. 3. Costa RA, Mintz GS, Carlier SG, Lansky AJ, Moussa I, Fujii K, et al...

Journal: :The European respiratory journal 1995
K Takahashi H Takahashi K Maeda S Homma T Uekusa T Dambara S Kira

Pulmonary lymphangiomatosis is a rare clinical and pathological entity which is distinct from lymphangiomyomatosis and from pulmonary lymphangiectasis. We report a case of a 20 year old man with diffuse lymphangiomatosis involving the mediastinum, lungs and retroperitoneum. The patient's intrathoracic lymphangiomatosis produced restrictive and obstructive impairment of his pulmonary function, b...

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