The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case

Volume: 38 Number: 3 September 1, 2012
  • Nermin Keni
  • Vildan Özkocaman
  • Fahir Özkalemkaş
  • Rıdvan Ali
  • Gönül Irmak
  • İrfan Esen
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Journal of Uludağ University Medical Faculty
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The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case

Abstract

The association of Evans sydrome which has tendency to bleeding with thrombophilic condition which has tendency to thrombosis is too rare. Our 40 years male case was diagnosed with immun thrombocitopenic purpura (İTP) in March 2009 (thrombocyte: 5710). On his follow-up after three mounts deep venous thrombosis (DVT) developed. Then upon investigation of history, clinic and laboratory of the case we found heterozygous factor V mutation. Treatment with low molecule weight heparine (LMWH) was administered during one year. After 7 mounts of diagnosis splenectomy was performed as a second line therapy because of recurren İTP relapses and afterward he remained in remission. After 7 mounts of splenectomy our case was diagnosed with Evans sydrome while researching the anemia which was detected just at that time. After 16 mounts of splenectomy second deep venous thrombosis event occured, than we planned long term treatment with DMWH. Our patient was lost with a sudden death after 19 mounts of splenectomy probably due to a new event associated with thrombosis.

Keywords

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Primary Language

English

Subjects

-

Journal Section

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Authors

Nermin Keni This is me

Vildan Özkocaman This is me

Fahir Özkalemkaş This is me

Rıdvan Ali This is me

Gönül Irmak This is me

İrfan Esen This is me

Publication Date

September 1, 2012

Submission Date

September 1, 2012

Acceptance Date

-

Published in Issue

Year 2012 Volume: 38 Number: 3

IZ

https://izlik.org/JA25JT74DY

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RIS / Bibtex
APA
Keni, N., Özkocaman, V., Özkalemkaş, F., Ali, R., Irmak, G., & Esen, İ. (2012). The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case. Journal of Uludağ University Medical Faculty, 38(3), 207-209. https://izlik.org/JA25JT74DY
AMA
1.Keni N, Özkocaman V, Özkalemkaş F, Ali R, Irmak G, Esen İ. The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case. Journal of Uludağ University Medical Faculty. 2012;38(3):207-209. https://izlik.org/JA25JT74DY
Chicago
Keni, Nermin, Vildan Özkocaman, Fahir Özkalemkaş, Rıdvan Ali, Gönül Irmak, and İrfan Esen. 2012. “The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case”. Journal of Uludağ University Medical Faculty 38 (3): 207-9. https://izlik.org/JA25JT74DY.
EndNote
Keni N, Özkocaman V, Özkalemkaş F, Ali R, Irmak G, Esen İ (September 1, 2012) The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case. Journal of Uludağ University Medical Faculty 38 3 207–209.
IEEE
[1]N. Keni, V. Özkocaman, F. Özkalemkaş, R. Ali, G. Irmak, and İ. Esen, “The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case”, Journal of Uludağ University Medical Faculty, vol. 38, no. 3, pp. 207–209, Sept. 2012, [Online]. Available: https://izlik.org/JA25JT74DY
ISNAD
Keni, Nermin - Özkocaman, Vildan - Özkalemkaş, Fahir - Ali, Rıdvan - Irmak, Gönül - Esen, İrfan. “The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case”. Journal of Uludağ University Medical Faculty 38/3 (September 1, 2012): 207-209. https://izlik.org/JA25JT74DY.
JAMA
1.Keni N, Özkocaman V, Özkalemkaş F, Ali R, Irmak G, Esen İ. The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case. Journal of Uludağ University Medical Faculty. 2012;38:207–209.
MLA
Keni, Nermin, et al. “The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case”. Journal of Uludağ University Medical Faculty, vol. 38, no. 3, Sept. 2012, pp. 207-9, https://izlik.org/JA25JT74DY.
Vancouver
1.Nermin Keni, Vildan Özkocaman, Fahir Özkalemkaş, Rıdvan Ali, Gönül Irmak, İrfan Esen. The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case. Journal of Uludağ University Medical Faculty [Internet]. 2012 Sep. 1;38(3):207-9. Available from: https://izlik.org/JA25JT74DY

ISSN: 1300-414X, e-ISSN: 2645-9027

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