Case Report
BibTex RIS Cite

The Surgical Treatment of Deep Vein Thrombosis

Year 1975, Volume: 28 Issue: 1-2, 289 - 306, 30.06.1975

Abstract

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.

References

  • 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.

Derin Ven Trombozlarında Cerrahi Tedavi

Year 1975, Volume: 28 Issue: 1-2, 289 - 306, 30.06.1975

Abstract

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.

References

  • 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.
There are 21 citations in total.

Details

Primary Language Turkish
Subjects General Surgery
Journal Section Articles
Authors

Ragıp Çam This is me

Publication Date June 30, 1975
Published in Issue Year 1975 Volume: 28 Issue: 1-2

Cite

APA Çam, R. (1975). Derin Ven Trombozlarında Cerrahi Tedavi. Ankara Üniversitesi Tıp Fakültesi Mecmuası, 28(1-2), 289-306.
AMA Çam R. Derin Ven Trombozlarında Cerrahi Tedavi. Ankara Üniversitesi Tıp Fakültesi Mecmuası. June 1975;28(1-2):289-306.
Chicago Çam, Ragıp. “Derin Ven Trombozlarında Cerrahi Tedavi”. Ankara Üniversitesi Tıp Fakültesi Mecmuası 28, no. 1-2 (June 1975): 289-306.
EndNote Çam R (June 1, 1975) Derin Ven Trombozlarında Cerrahi Tedavi. Ankara Üniversitesi Tıp Fakültesi Mecmuası 28 1-2 289–306.
IEEE R. Çam, “Derin Ven Trombozlarında Cerrahi Tedavi”, Ankara Üniversitesi Tıp Fakültesi Mecmuası, vol. 28, no. 1-2, pp. 289–306, 1975.
ISNAD Çam, Ragıp. “Derin Ven Trombozlarında Cerrahi Tedavi”. Ankara Üniversitesi Tıp Fakültesi Mecmuası 28/1-2 (June1975), 289-306.
JAMA Çam R. Derin Ven Trombozlarında Cerrahi Tedavi. Ankara Üniversitesi Tıp Fakültesi Mecmuası. 1975;28:289–306.
MLA Çam, Ragıp. “Derin Ven Trombozlarında Cerrahi Tedavi”. Ankara Üniversitesi Tıp Fakültesi Mecmuası, vol. 28, no. 1-2, 1975, pp. 289-06.
Vancouver Çam R. Derin Ven Trombozlarında Cerrahi Tedavi. Ankara Üniversitesi Tıp Fakültesi Mecmuası. 1975;28(1-2):289-306.