Microangiopathic haemolytic anaemia and the pathogenesis of malignant hypertension.
نویسندگان
چکیده
S 873 SICKLE CELL ( Hb-S ) TRAIT IN FAMILY FROM SERBIA-YUGOSLAvIA. A. Sadikario, II. Duma, B. Mladenovski, G. Efremov, M. Andreeva and C. Lazova. From Department of Pediatrics, University of Skopje, Yugoslavia. J. Ped. Ass. Yugo. 11:
منابع مشابه
Erythrocytes Microangiopathic Haemolytic Anaemia and the Pathogenesis of Malignant Hypertension
S 873 SICKLE CELL ( Hb-S ) TRAIT IN FAMILY FROM SERBIA-YUGOSLAvIA. A. Sadikario, II. Duma, B. Mladenovski, G. Efremov, M. Andreeva and C. Lazova. From Department of Pediatrics, University of Skopje, Yugoslavia. J. Ped. Ass. Yugo. 11:
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A case of microangiopathic haemolytic anaemia associated with malignant haemangio-endothelioma is described. It is suggested that haemolysis may have been due to mechanical trauma sustained by the red blood cells on passage through the tumour's abnormal vasculature.
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A 42-year-old woman presented with a huge benign pelvic tumour and recurrent pulmonary emboli associated with severe microangiopathic haemolytic anaemia (MAHA). Following removal of the tumour and anticoagulation, all signs of MAHA disappeared. MAHA may occur when red blood cells pass through abnormal blood vessels in tumours. This patient is unusual in that the tumour was benign, rather than m...
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متن کاملThrombotic microangiopathic haemolytic anaemia.
The syndrome of thrombotic microangiopathic haemolytic anaemia is rare and almost all the cases reported have been in adults. Very few cases occurring in childhood have been reported and the youngest recorded case was 22 months old (Craig and Gitlin, 1957). We report the clinical and pathological details and the response to treatment of a child aged 21 months, who was seen at the Austin Hospita...
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ورودعنوان ژورنال:
- Lancet
دوره 1 7609 شماره
صفحات -
تاریخ انتشار 1969