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Czasopismo
2015 | 74 | 1 |
Tytuł artykułu

Absence of the suprarenal segment of the inferior vena cava with a coexisting absence of the right brachiocephalic vein in a 22-year-old Caucasian male with arterial hypertension

Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Congenital anomalies of the inferior vena cava (IVC) are rarely observed malformations of the venous system, occurring in 0.3% of otherwise healthy individuals, and in 0.6% to 2% of patients with coexisting cardiovascular defects. They are usually asymptomatic and recognised incidentally during imaging, operations or dissection studies. In this paper we report an extremely rare case of a 22-year-old Caucasian male, admitted for the purpose of excluding secondary causes of hypertension. During imaging of the abdomen and the thorax we found a complete lack of the suprarenal segment of the IVC, with a coexisting absence of the right brachiocephalic vein. We discuss the problem of congenital defects of the IVC and we review the relevant literature. (Folia Morphol 2015; 74, 1: 122–126)
Słowa kluczowe
Wydawca
-
Czasopismo
Rocznik
Tom
74
Numer
1
Opis fizyczny
p.122-126,fig.,ref.
Twórcy
autor
  • Department of Internal Diseases, Metabolic Disorders and Arterial Hypertension, Poznan University of Medical Sciences, Szamarzewskiego 84, 60–569 Poznan, Poland
autor
  • Department of Radiology, Clinical Hospital of Transfiguration, Poznan University of Medical Sciences, Poznan, Poland
autor
  • Department of Radiology, Clinical Hospital of Transfiguration, Poznan University of Medical Sciences, Poznan, Poland
  • Department of Radiology, Clinical Hospital of Transfiguration, Poznan University of Medical Sciences, Poznan, Poland
  • Department of Neuroradiology, Poznan University of Medical Sciences, Poznan, Poland
autor
  • Department of Internal Diseases, Metabolic Disorders and Arterial Hypertension, Poznan University of Medical Sciences, Poznan, Poland
autor
  • Department of Internal Diseases, Metabolic Disorders and Arterial Hypertension, Poznan University of Medical Sciences, Poznan, Poland
Bibliografia
  • 1. Abdullah A, Williamson K, Lewis T, Elsamaloty H (2011) Variant central intrahepatic course of interior vena cava: volume-rendering and maximum intensity projection CT findings. Br J Radiol, 84: e135–e137.
  • 2. Chuang VP, Mena CE, Hoskins PA (1974) Congenital anomalies of the inferior vena cava. Review of embryogenesis and presentation of a simplified classification. Br J Radiol, 47: 206–213.
  • 3. Gayer G, Luboshitz J, Hertz M, Zissin R, Thaler M, Lubetsky A, Bass A, Korat A, Apter S (2003) Congenital anomalies of the interior vena cava revealed on CT in patients with deep vein thrombosis. Am J Roentgenol, 180: 729–732.
  • 4. Gayer G, Zissin R, Strauss S, Hertz M (2003) IVC anomalies and right renal aplasia detected on CT: a possible link? Abdominal Imaging, 28: 395–399.
  • 5. Guérin F, Blanc Th, Gauthier F, Franchi Abella S, Branchereau S (2012) Congenital portosystemic vascular malformations. Seminars in Pediatric Surgery, 21: 233–244.
  • 6. Guo FF, Shao ZQ, Li HL, Wang GJ, Zhu WB (2011) Successful use of the dilated right spermatic cord vein for renal transplantation in a patient with congenital hypoplasia of the interior vena cava. Transplantation Proceeding,43: 4002–4004.
  • 7. Joskin J, Bleus N, Couvreur T, Tselikas L, Milicevic M (2012) Duplicate inferior vena cava continuing as a hemiazygos continuation draining into the right atrium via persistent left superior vena cava. JBR–BTR, 95: 174.
  • 8. Kapetanakis S, Papadopoulos C, Galani P, Dimitrakopoulou G, Fiska A (2010) Anomalies of the interior vena cava: a report of two cases and a short review of the literature. Folia Morphol, 69: 123–127.
  • 9. Kouroukis Ch, Leclerc JR (1996) Pulmonary embolism with duplicated vena cava. Chest, 109: 1111–1113.
  • 10. Mutlu GY, Ramot Y, Babaoglu K, Altun G, Zlotogorski A, Molho-Pessach V (2013) Agenesis of the inferior vena cava in H syndrome due to a novel SLC29A3 mutation. Pediatric Dermatol, 30: e70–e73.
  • 11. Nseir W, Mahamid M, Abu-Rahmed Z, Markel A (2011) Recurrent deep venous thrombosis in a patient with agenesis of inferior vena cava. Int J Gen Med, 4: 457–459.
  • 12. Obernosterer A, Aschauer M, Mitterhammer H, Lipp RW (2004) Congenital familial vascular anomalies: a study of patients with an anomalous inferior vena cava, and of their first degree relatives. Angiology, 55: 73–77.
  • 13. Obernosterer A, Aschauer M, Schnedl W, Lipp RW (2002) Anomalies of the interior vena cava in patients with iliac venous thrombosis. Ann Intern Med, 136: 37–41.
  • 14. Ruggeri M, Tosetto A, Castaman G, Rodeghiero F (2001) Congenital absence of the inferior vena cava: a rare risk factor for idiopathic deep-vein thrombosis. Lancet, 357: 441.
  • 15. Timmers GJ, Falke TH, Rauwerda JA, Huijgens PC (1999) Deep vein thrombosis as a presenting symptom of congenital interruption of the inferior vena cava. Int J Clin Pract, 53: 75–76.
  • 16. Tore HG, Tatar I, Celik HH, Oto A, Aldur MM, Denck CC (2005) Two cases of interior vena cava duplication with their CT findings and a review of literature. Folia Morphol, 64: 55–58.
  • 17. Yugueros X, Alvarez B, Fernandez E, Boque M, Matas M (2013) Compressive symptoms due to thrombosed or hypertrophic collateral circulation in infrarenal inferior vena cava agenesis. Ann Vasc Surg, 27: 238.e9–238.e13.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
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