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  • Küçük Resim
    Öğe
    An elderly patient with Bochdalek's hernia case that implies left-sided intratoracic renal ectopia
    (TIP ARASTIRMALARI DERNEGI, 2012) Önder, Hakan; Güler, Şükran; Tekbaş, Güven; Büyükkaya, Ayla; Gümüş, Hatice; Ekici, Faysal; Bilici, Aslan
    Bochdalek hernia is a congenital disease characterized by protrusion of the abdominal organs into the thorax through the posterior defect in the diaphragma. The detection of incidental bochdalek hernia has increased because of the widespread use of the multidedector computed tomography. It is very rare in adult population. Intrathoracic kidney in bochdalek hernia is uncommon. In this paper, a 78 year-old man who had bochdalek hernia with a kidney in the left side of the thoracic region is presented.
  • Küçük Resim
    Öğe
    An elderly patient with bochdaleks hernia case that ımplies left-sided ıntratoracic renal ectopia
    (2012) Önder, Hakan; Güler, Şükran; Tekbaş, Güven; Büyükkaya, Ayla; Gümüş, Hatice; Ekici, Faysal; Bilici, Aslan
    Bochdalek hernisi posterior diafragmadan abdominal organların toraks içerisine yer değiştirmesi ile karakterize konjenital bir hastalıktır.Bochdalek hernisinin insidental olarak tesbiti çok kesitli bilgisayarlı tomografinin(ÇKBT) yaygın kullanılmasıyla artmıştır.Bochdalek hernisi yaşlı kişilerde oldukça nadir görülmektedir. Herni içerisinde böbrek görülmesi de yaygın değildir.Bu yazıda toraksda solda, içerisinde sol böbrek ve kalın barsak ansları bulunan 78 yaşında bir olgu sunulmuştur.
  • Küçük Resim
    Öğe
    Pelvic And Bilateral Symetric Lower Extremities Involvement Of Extensive Fetal Cystic Lymphangioma: A Case Report
    (Düzce Üniversitesi, 2015) Dusak, Abdurrahim; Durmaz, Mehmet Sedat; Bilici, Aslan; Alan, Bircan
    Extensive fetal cystic lymphangioma is a rare congenital malformation of the lymphatic system.Their prognosis depends on the size and location of the lesions as well as other accompanyinganomalies. Our case was 35 years, fetal BPD was 27 weeks . Herein, we present a case ofextensive fetal cystic lymphangioma that began at the pelvic area and symmetrically spannedthe bilateral proximal and distal lower extremities. Numerous extensive and sharplycircumscribed, thin walled multilobular cystic lesions in different sizes were observed in thesubcutaneous superficial and deep soft tissue beginning from the pelvic area and extending toboth lower extremities to the distal in the fetüs. To our knowledge, a case involving bothextremities has not yet been reported in the literature