Ankara Üniversitesi Tıp Fakültesi Mecmuası

0365-8104 1307-5608

Ankara University

General Surgery

Genel Cerrahi

The Surgical Treatment of Deep Vein Thrombosis

Derin Ven Trombozlarında Cerrahi Tedavi

Çam

Ragıp

ANKARA UNIVERSITY, ANKARA FACULTY OF MEDICINE

06 30 1975

28 1-2 289 306 01 01 1975 06 29 1975

1947

Ankara Üniversitesi Tıp Fakültesi Mecmuası

The treatment of choice for acute iliofemoral thrombosis is immediate thrombectomy. This method offers several advantages over medical interventions. Thrombectomy will provide immediate relief of pain and swelling, minimize the risk of pulmonary embolism, and ultimately prevent the development of venous insufficiency.

Akut iliofemoral trombozis için seçilen tedavi yöntemi, hemen yapılacak trombektomidir. Medikal girişimlerle karşılaştırıldığında bu yöntemin birçok üstünlükleri vardır. Trombektomi, ağrı ve ödemin hemen kaybolmasını sağlıyacak, pulmoner emboli tehdidini en az orana indirecek ve nihayet venöz yetmezlik gelişmesini önleyecektir.

Derin ven trombozu trombektomi iliofemoral tromboz

Deep vein thrombosis thrombectomy iliofemoral thrombosis

1. Gerald, P., and Diamond, L. K.: A new hereditary Hb (the Lepore trait and its interaction with thalassemia). Blood 13: 835, 1958.

2. Gerald, P. et al.: Identification of chemical defect in the Lepore hemoglobin. Amer. J. Dis. Child. 100: 757, 1960.

3. Pearson, H. A. et al.: Erythrocynetics in thalassemia. II. Studies in Lepore trait and Hb H disease. J. Lab. and Clin. Med. 59: 147, 1962.

4. Pearson, H. A., Gerald, P., and Diamond, L. K.: Thalassemia intermediate due to interaction of Lepore trait with thalassemia. Amer. J. Dis. Child. 97: 464, 1959.

5. Williams, W. J. et al.: Hematology: The Lepore hemoglobins. New York, McGraw-Hill, p. 341, 1972.

6. Mauer, A. M.: Pediatric Hematology. McGraw-Hill, New York, p. 141, 1969.

7. Fessas, P. I. et al.: Hb «Pylos» study of hemoglobinopathy resembling thalassemia. Blood, 19: 1, 1962.

8. Barnabas, J., and Muller, J. C.: Hb-Lepore Hollandia. Nature, 194: 931, 1962.

9. Jonxis, J. H. D.: A thalassemia-like picture in a Papuan family. In «Hemoglobin Colloquim», p. 60, 1962.

10. Ramney, H. M., and Jacobs, A. S.: Simultaneous occurrence of hemoglobins C and Lepore in an Afro-American. Nature, 204: 463, 1964.

11. Beaven, G. H. et al.: An abnormal Hb (Lepore-Cyprus) resembling Hb-Lepore. Brit. J. Hemat. 10: 159, 1964.

12. Quattrin, N. et al.: Studies on 9 families with Hb Lepore in Compania. Acta Haemat. 37: 266, 1967.

13. Ostertag, W., and Smith, E. W.: Hb Lepore Baltimore: A third type of δ-β crossover. Europ. J. Biochem., 10: 371, 1969.

14. Ohta, Y. et al.: Hb Miyada, a β-δ fusion peptide (Anti-Lepore) discovered in a Japanese family. Nature, 234: 218, 1971.

15. Porter, I. H.: Heredity and disease. McGraw-Hill, p. 167, 351, 1967.

16. Çavdar, A. O., Arcasoy, A.: The incidence of β thalassemia and abnormal hemoglobins in Turkey. Acta Hemat., 45: 312, 1971.

17. Çavdar, A. et al.: Hematological and Biochemical Findings in Turkish Children with Pica. Clin. Ped., 11: 215, 1972.

18. Lehmann, H. et al.: Man's Hemoglobins. North-Holland, p. 154-155, 1966.

19. Rahbar, S. et al.: Hemoglobin Lepore Boston in two Iranian Families. Blood., 42: 79, 1974.

20. Duma, H. et al.: Study of nine families with hemoglobin-Lepore. Brit. J. Hematology., 15: 161, 1968.

21. Efremov, G. D. et al.: Chemical Heterogeneity of Fetal Hb in the Lepore Hemoglobinopathy. Brit. J. Hemat., 27: 319, 1974.