Case Report
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Servikal aortik ark

Year 2020, Volume: 3 Issue: 2, 187 - 189, 19.03.2020
https://doi.org/10.32322/jhsm.479578

Abstract

Servikal
aortik ark, nadir görülen bir konjenital anomalidir. Çocuklukta genellikle
semptomatiktir, ancak asemptomatik erişkinlerde bazen bu anormallik farklı
nedenlerden dolayı radyolojik görüntüleme sırasında teşhis edilir. Biz bu
yazıda öksürük ve nefes darlığı ile başvuran servikal aortik ark olgusunu ve
literatürün gözden geçirilmesini amaçladık.

References

  • 1. Jaffe RB. Complete interruption of the aortic arch. Characteristic angiographic features with emphasison collateral circulation to the descending aorta. Circulation 1976; 53(1): 161-8.
  • 2. Baravelli M, Borghi A, Rogiani S, et al. Clinical, anatomopathological and genetic pattern of 10 patients with cervical aortic arch. Int J Cardiol 2007; 114(2): 236-40.
  • 3. Haughton VM, Fellows KE, Rosenbaum AE. The cervical aortic arches. Radiology 1975; 114(3): 675-81.
  • 4. Higuchi K, Koseni K, Takamoto S. Left-sided cervical aortic arch aneurysm: case report. J Thorac Cardiovasc Surg 2003; 126(6): 2098-100.
  • 5. Ilyas M, Shah SA, Gojwari T, Sheikh WA. Cervical aortic arch—when the aorta gets high. Indian J Thorac Cardiovasc Surg 2018;34:521-4.
  • 6. Makani S, Mitchell J, Metton O, et al. Surgical repair of a pseudocoarctation with cervical aortic arch complicated by multiple aneurysms of the aorta: a case report. Pan Afr Med J 2017; 26: 236.

Cervical aortic arch

Year 2020, Volume: 3 Issue: 2, 187 - 189, 19.03.2020
https://doi.org/10.32322/jhsm.479578

Abstract

Cervical aortic arch is an unusual
congenital anomaly.
It
is usually symptomatic in childhood, but sometimes this abnormality is
diagnosed during radiological examination because of unrelated causes in
asymptomatic adults.  We aimed to report
a case of cervical aortic arch and
review of the literature  which  presented
with cough and shortness of breath. 

References

  • 1. Jaffe RB. Complete interruption of the aortic arch. Characteristic angiographic features with emphasison collateral circulation to the descending aorta. Circulation 1976; 53(1): 161-8.
  • 2. Baravelli M, Borghi A, Rogiani S, et al. Clinical, anatomopathological and genetic pattern of 10 patients with cervical aortic arch. Int J Cardiol 2007; 114(2): 236-40.
  • 3. Haughton VM, Fellows KE, Rosenbaum AE. The cervical aortic arches. Radiology 1975; 114(3): 675-81.
  • 4. Higuchi K, Koseni K, Takamoto S. Left-sided cervical aortic arch aneurysm: case report. J Thorac Cardiovasc Surg 2003; 126(6): 2098-100.
  • 5. Ilyas M, Shah SA, Gojwari T, Sheikh WA. Cervical aortic arch—when the aorta gets high. Indian J Thorac Cardiovasc Surg 2018;34:521-4.
  • 6. Makani S, Mitchell J, Metton O, et al. Surgical repair of a pseudocoarctation with cervical aortic arch complicated by multiple aneurysms of the aorta: a case report. Pan Afr Med J 2017; 26: 236.
There are 6 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Case Report
Authors

Sefa Türkoğlu This is me 0000-0002-9623-0083

Cihan Bedel 0000-0002-3823-2929

Publication Date March 19, 2020
Published in Issue Year 2020 Volume: 3 Issue: 2

Cite

AMA Türkoğlu S, Bedel C. Cervical aortic arch. J Health Sci Med / JHSM. March 2020;3(2):187-189. doi:10.32322/jhsm.479578

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Assoc. Prof. Alpaslan TANOĞLU (MD)  

Prof. Aydın ÇİFCİ (MD)

Prof. İbrahim Celalaettin HAZNEDAROĞLU (MD)

Prof. Murat KEKİLLİ (MD)

Prof. Yavuz BEYAZIT (MD) 

Prof. Ekrem ÜNAL (MD)

Prof. Ahmet EKEN (MD)

Assoc. Prof. Ercan YUVANÇ (MD)

Assoc. Prof. Bekir UÇAN (MD) 

Assoc. Prof. Mehmet Sinan DAL (MD)


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