Cerebral Sinus Thrombosis During Pregnancy Associated with Protein S Deficiency: Report of a Rare Case

Yıl 2014, Cilt: 21 Sayı: 4, 307 - 309, 01.08.2014

Murat Bulanık Zeynep Özcan Dağ Demet Demiray Ersel Dağ Yavuz Şimşek

Öz

Hereditary thrombophylic mutations are seen in 10% of the general population and many cases are diagnosed as a result of complications that occur during pregnancy. Of these, Protein S deficiency is a rare hereditary trombophilia with severe thrombogenic features. Pregnancies accompanying protein S deficiency often result in loss of fetus. In this paper, we present the case of a protein S deficiency patient who eventually had a live birth despite the cerebral sinus thrombosis in the 30th week of her pregnancy and discuss the case with references to the relevant literature. Key words: Protein S Deficiency; Hereditary Thrombophilia; Cerebral Sinus Trombosis; Pregnancy.

Anahtar Kelimeler

Protein S Deficiency; Hereditary Thrombophilia; Cerebral Sinus Trombosis; Pregnancy.

Gebelite Protein-S Eksikliği İle İlişkili Serebral Sinüs Trombozu: Nadir Bir Olgu Sunumu

Öz

Herediter trombofilik mutasyonlar genel popülasyonun %10'unda görülür ve bir çok olgu gebelik sırasında ortaya çıkan komplikasyonlar sonucunda tanı alır. Bunlardan Protein S eksikliği nadir görülen ve şiddetli trombojenik özellikte bir herediter trombofiliadır. Protein S eksikliği eşlik eden gebelikler genelde fetal kayıpla sonuçlanır. Bu yazıda canlı doğumla son bulan gebeliği sırasında, 30. gebelik haftasında serebral sinüs trombozu geçiren ve tetkiklerinde protein S eksikliği saptanan bir olgu sunularak konu literatür bilgileri eşliğinde tartışıldı. Anahtar kelimeler: Protein S Eksikliği; Herediter Trombofilia; Serebral Sinüs Trombozu; Gebelik.

Anahtar Kelimeler

Protein S Eksikliği; Herediter Trombofilia; Serebral Sinüs Trombozu; Gebelik.

Kaynakça

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