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1.
Indian J Chest Dis Allied Sci ; 1989 Oct-Dec; 31(4): 259-64
Artículo en Inglés | IMSEAR | ID: sea-29356

RESUMEN

A prospective study of pleural fluid eosinophilia (PFE) during initial thoracocentesis in 162 patients of pleural effusion was undertaken to determine its value in establishing an etiological diagnosis. Eighteen of the 162 cases showed pleural fluid eosinophilia (PFE), twelve could not be labelled with any definitive etiology even after extensive investigations, four belonged to the para-pneumonic group and resolved with treatment. Of the 32 patients with malignancy, PFE was seen in a single case of pleural mesothelioma. None of the patients with tuberculosis, empyema, systemic lupus erythematosus or amoebiasis had PFE. These findings suggest that PFE seen at initial thoracocentesis favours a benign diagnosis, with a rare chance of malignancy. Tuberculosis is unlikely in such patients.


Asunto(s)
Biopsia con Aguja , Diagnóstico Diferencial , Eosinofilia/diagnóstico , Humanos , Enfermedades Pulmonares/diagnóstico , Enfermedades Pleurales/diagnóstico , Derrame Pleural/diagnóstico , Estudios Prospectivos
2.
Artículo en Inglés | IMSEAR | ID: sea-92351

RESUMEN

A case of congenital afibrinogenaemia in a young female child is described. She had haemorrhagic tendency since birth in the form of markedly prolonged umbilical bleeding and easy bruising afterwards. Two of her brothers had bleeding tendencies, one died shortly after birth due to uncontrollable umbilical bleeding and other died at the age of 12 years from internal haemorrhage. The family study indicates the mode of inheritance to be probably autosomal recessive. The principal laboratory findings are complete non-coagulability of blood, grossly abnormal coagulation tests, zero ESR value, failure to detect fibrinogen by heat coagulation or chemical precipitation tests and biuret reaction and correction of thrombin time after fibrinogen infusion.


Asunto(s)
Afibrinogenemia/genética , Pruebas de Coagulación Sanguínea , Niño , Femenino , Fibrinógeno/administración & dosificación , Trastornos Hemorrágicos/genética , Humanos
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