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  • Küçük Resim
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    Intracavitary lesion caused by bladder wall stone and mimicking bladder tumor
    (2019) Topçu, İbrahim; Oğuz, Fatih; Geçit, İlhan; Sancaktar, Fatih; Akatlı, Ayşe Nur
    Abstract: We present a 28 year-old patient with insidental intramural stone covered by bladder mass. The pathology was rarely seen cystitisglandularis with intestinal metaplasia. During cystoscopy, stone was not seen, we resected the mass than stone was appeared inburied into the wall and removed from the bladder wall. The stone was fragmented with holmium laser. The pathology of the masswas cystitis glandularis with intestinal metaplasia whish is rarely seen and may be malign by the time. We followed up the patientwith cystoscopy every 3 months and no recurrens was detected.
  • Küçük Resim
    Öğe
    Intracavitary lesion caused by bladder wall stone and mimicking bladder tumor
    (2019) Topcu; Ibrahim; Oguz, Fatih; Gecit, Ilhan; Akatli, Ayse Nur; Sancaktar, Fatih
    We present a 28 year-old patient with insidental intramural stone covered by bladder mass. The pathology was rarely seen cystitis glandularis with intestinal metaplasia. During cystoscopy, stone was not seen, we resected the mass than stone was appeared in buried into the wall and removed from the bladder wall. The stone was fragmented with holmium laser. The pathology of the mass was cystitis glandularis with intestinal metaplasia whish is rarely seen and may be malign by the time. We followed up the patient with cystoscopy every 3 months and no recurrens was detected.
  • Küçük Resim
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    Postpartum Dönemde Homozigot Faktör-V Leiden Mutasyonuna Bağlı Akut Budd-Chiari Sendromu
    (Fırat Tıp Dergisi, 2017) Bilgiç, Yılmaz; Cengiz, Muhammet; Cengiz, Ayşe Nuransoy; Yılmaz, Cengiz; Çağın, Yasir Furkan; Sancaktar, Fatih; Yıldırım, Oğuzhan
    Öz: Budd--Chiari Sendromuküçük hepatik verilerden sağ atriuma kadar olan damarsal yapılarda ortaya çıkan darlık veya obstrüksiyonlar sonucunda karaciğer venöz dönüşünün bozulmuş olduğunadir görülen bir durumdur. Klinik spektrumu, kronik asemptomatik hast alıktarı akut fulminan karaci-- ğer yetmezliği arasında değişkenlik gösterir ve karaciğer sirozu ile neticelenebilir. Trombotiliye eğilim oluşturan kalıtsal veya edinsel nedenler, damar sistemine dıştan bası gibi birçok neden etiyolojide yer alır. Gebelik ve postpartum dönem tromboza eğilimi arttırır. Yazımızda postpartum dönemde akut Budd--Chiari Sendromutamsı konulmuş olanve Faktör--V Leiden mutasyonuhomozigot pozitif saptanmış olan nadir bir vakayı sunmaktayız. Başlık (İngilizce): A C ase of Acute Budd-Chiari Syndrome Due to Homozygous Factor-V Leiden Mutation in the Postpartum Period Öz (İngilizce): Budd-Chiari Syndrome is a rare disorder charecterized by obstruction of hepatic outflow tract at any level between small hepati c venules and right atrium. Clinical spectrum changes in a range between chronic asymptomatic patients to fulminant liver failure, it may also re sults with cirrhosis. T here are many etiologies of the syndrome like inherited and secondary thrombophilias and external compression of veins. Pregnancy and postpartum period increase the tendency to thrombosis. In this paper, we presented a rare case of acute Budd Chiari syndrome, which was found to be homozygous for factor-V leiden mutation in the postpartum period.