Evans Sendromlu Olguda Tekrarlayan Derin Ven Trombozu Atakları ve Faktör V Leiden Heterozigot Mutasyon Birlikteliği: Nadir Bir Olgu

Cilt: 38 Sayı: 3 1 Eylül 2012
  • Nermin Keni
  • Vildan Özkocaman
  • Fahir Özkalemkaş
  • Rıdvan Ali
  • Gönül Irmak
  • İrfan Esen
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The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case

Öz

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.

Anahtar Kelimeler

Ayrıntılar

Birincil Dil

İngilizce

Konular

-

Bölüm

-

Yazarlar

Nermin Keni Bu kişi benim

Vildan Özkocaman Bu kişi benim

Fahir Özkalemkaş Bu kişi benim

Rıdvan Ali Bu kişi benim

Gönül Irmak Bu kişi benim

İrfan Esen Bu kişi benim

Yayımlanma Tarihi

1 Eylül 2012

Gönderilme Tarihi

1 Eylül 2012

Kabul Tarihi

-

Yayımlandığı Sayı

Yıl 2012 Cilt: 38 Sayı: 3

IZ

https://izlik.org/JA25JT74DY

Kaynak Göster

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. Uludağ Tıp Derg. 2012;38(3):207-209. https://izlik.org/JA25JT74DY
Chicago
Keni, Nermin, Vildan Özkocaman, Fahir Özkalemkaş, Rıdvan Ali, Gönül Irmak, ve 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 (01 Eylül 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, ve İ. Esen, “The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case”, Uludağ Tıp Derg, c. 38, sy 3, ss. 207–209, Eyl. 2012, [çevrimiçi]. Erişim adresi: 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 (01 Eylül 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. Uludağ Tıp Derg. 2012;38:207–209.
MLA
Keni, Nermin, vd. “The Association of Evans Syndrome and Recurrent Deep Venous Thrombosis With Factor V Heterozygous Mutation: A Rare Case”. Journal of Uludağ University Medical Faculty, c. 38, sy 3, Eylül 2012, ss. 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. Uludağ Tıp Derg [Internet]. 01 Eylül 2012;38(3):207-9. Erişim adresi: https://izlik.org/JA25JT74DY

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

Uludağ Üniversitesi Tıp Fakültesi Dergisi "Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License" ile lisanslanmaktadır.


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Journal of Uludag University Medical Faculty is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

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