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2018 | 77 | 1 |

Tytuł artykułu

A rare vascular anomaly in the form of double left brachiocephalic vein detected incidentally during cardiac implantable electronic device (CIED) placement

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The growing number of transvenous cardiac implantable electronic device (CIED) implantation procedures helps detect rare vascular anomalies. Genetic disturbances in vascular development can produce systemic vein anomalies, including the left brachiocephalic vein (BCV). BCV anomalies commonly coexist with a persistent left superior vena cava (PLSVC), detected in 0.3–0.5% of the general population. The three known anatomical variations of PLSVC are two variations involving a BCV bridge and the third with BCV agenesis. BCV anomalies occur in 1% of patients with congenital heart defects, whereas the estimated proportion of BCV anomalies in the population with no cardiovascular symptoms is below 0.4%. A rarely observed, and thus rarely reported, BCV variation is a double left BCV, with the additional vessel typically found inferior and posterior to the ascending aorta prior to draining into the superior vena cava. This case report presents a previously unreported variation of double left BCV, with both vessels coursing parallel to each other, superior to the aortic arch. (Folia Morphol 2018; 77, 1: 161–165)

Słowa kluczowe

Wydawca

-

Czasopismo

Rocznik

Tom

77

Numer

1

Opis fizyczny

p.161-165,fig.,ref.

Twórcy

  • Department of Cardiology, Medical University of Warsaw, Warsaw, Poland
autor
  • Department of Cardiology, Medical University of Warsaw, Warsaw, Poland
autor
  • Department of Cardiology, Medical University of Warsaw, Warsaw, Poland

Bibliografia

  • 1. Chen SJ, Liu KL, Chen HY, et al. Anomalous brachiocephalic vein: CT, embryology, and clinical implications. AJR Am J Roentgenol. 2005; 184(4): 1235–1240, doi: 10.2214/ajr.184.4.01841235, indexed in Pubmed: 15788602.
  • 2. Chern MS, Ko JS, Tsai A, et al. Aberrant left brachiocephalic vein: CT imaging findings and embryologic correlation. Eur Radiol. 1999; 9(9): 1835–1839, indexed in Pubmed: 10602959.
  • 3. Corno AF, Alahdal SA, Das KM. Systemic venous anomalies in the Middle East. Front Pediatr. 2013; 1: 1, doi: 10.3389/fped.2013.00001, indexed in Pubmed: 24400249.
  • 4. Ghadiali N, Teo LM, Sheah K. Bedside confirmation of a persistent left superior vena cava based on aberrantly positioned central venous catheter on chest radiograph. Br J Anaesth. 2006; 96(1): 53–56, doi: 10.1093/bja/aei272, indexed in Pubmed: 16311276.
  • 5. Gülsün M, Gökoğlu A, Ariyürek M, et al. Subaortic left brachiocephalic vein: computed tomography and magnetic resonance angiography findings. Surg Radiol Anat. 2003; 25(3-4): 335–338, doi: 10.1007/s00276-003-0120-3, indexed in Pubmed: 12910378.
  • 6. Hindricks G, Camm J, Merkely B, et al. The EHRA White Book. 2016: 375–384.
  • 7. Kahkouee S, Sadr M, Pedarzadeh E, et al. Anomalous left brachiocephalic vein: important vascular anomaly concomitant with congenital anomalies and heart diseases. Folia Morphol. 2017; 76(1): 51–57, doi: 10.5603/FM.a2016.0031, indexed in Pubmed: 27830886.
  • 8. Kawamura I, Hojo R, Fukamizu S. A case of pacemaker implantation in the patient with duplication of the left innominate vein: a case report. Springerplus. 2016; 5:515, doi: 10.1186/s40064-016-2182-9, indexed in Pubmed: 27186479.
  • 9. Kawashima T, Sato K, Sato F, et al. An anatomical study of the human cardiac veins with special reference to the drainage of the great cardiac vein. Ann Anat. 2003; 185(6): 535–542, doi: 10.1016/S0940-9602(03)80122-X, indexed in Pubmed: 14703998.
  • 10. Ko SF, Huang CC, Ng SH, et al. Imaging of the brachiocephalic vein. AJR Am J Roentgenol. 2008; 191(3): 897–907, doi: 10.2214/AJR.07.3552, indexed in Pubmed: 18716126.
  • 11. Kondrachuk O, Yalynska T, Tammo R. Double left brachiocephalic vein. Pediatr Cardiol. 2013; 34(3): 767–768, doi: 10.1007/s00246-012-0542-y, indexed in Pubmed: 23052674.
  • 12. Kulkarni S, Jain S, Kasar P, et al. Retroaortic left innominate vein - Incidence, association with congenital heart defects, embryology, and clinical significance. Ann Pediatr Cardiol. 2008; 1(2): 139–141, doi: 10.4103/0974-2069.43881, indexed in Pubmed: 20300257.
  • 13. Kwon O, Lim J, Lee J, et al. Double left brachiocephalic veins with persistent left superior vena cava: a case report. J Korean Society Radiol. 2014; 71(2): 55, doi: 10.3348/jksr.2014.71.2.55.
  • 14. Nagashima M, Shikata F, Okamura T, et al. Anomalous subaortic left brachiocephalic vein in surgical cases and literature review. Clin Anat. 2010; 23(8): 950–955, doi: 10.1002/ca.21046, indexed in Pubmed: 20830788.
  • 15. Povoski SP, Khabiri H. Persistent left superior vena cava: review of the literature, clinical implications, and relevance of alterations in thoracic central venous anatomy as pertaining to the general principles of central venous access device placement and venography in cancer patients. World J Surg Oncol. 2011; 9: 173, doi: 10.1186/1477-7819-9-173, indexed in Pubmed: 22204758.
  • 16. Steckiewicz R, Kosior DA, Rosiak M, et al. The prevalence of superior vena cava anomalies as detected in cardiac implantable electronic device recipients at a tertiary cardiology centre over a 12-year period. Hellenic J Cardiol. 2016; 57(2): 101–106, doi: 10.1016/j.hjc.2016.03.003, indexed in Pubmed: 27445024.
  • 17. Takada Y, Narimatsu A, Kohno A, et al. Anomalous left brachiocephalic vein: CT findings. J Comput Assist Tomogr. 1992; 16(6): 893–896, indexed in Pubmed: 1430437.
  • 18. Topcuoglu OM, Atceken Z, Ariyurek OM. Circumaortic doubled left brachiocephalic vein: a rare confusing variation. Surg Radiol Anat. 2015; 37(3): 315–318, doi: 10.1007/s00276-014-1345-z, indexed in Pubmed: 25037739.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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