Giant Pericardial Tube Roll Aneurysm after the Treatment of Aortic Interruption

Mustafa O. Ulukan; Yahya Yildiz; Emin C. Ata; Didem M. Oztas; Korhan Erkanli; Murat Ugurlucan; Halil Turkoglu

doi:10.1055/s-0040-1714122

Giant Pericardial Tube Roll Aneurysm after the Treatment of Aortic Interruption

Aorta ◽

10.1055/s-0040-1714122 ◽

2020 ◽

Vol 08 (05) ◽

pp. 152-154

Author(s):

Mustafa O. Ulukan ◽

Yahya Yildiz ◽

Emin C. Ata ◽

Didem M. Oztas ◽

Korhan Erkanli ◽

...

Keyword(s):

Aortic Arch ◽

Interrupted Aortic Arch ◽

Newborn Period ◽

Graft Interposition ◽

Aortic Interruption

AbstractVarious techniques have been described for the treatment of interrupted aortic arch pathology. Graft interposition, either autologous or synthetic, is included among these methods. In this article, we present the images of giant pericardial roll aneurysm that was used for the treatment of aortic interruption during the newborn period.

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Interrupted Aortic Arch or Extreme Coarctation? A Case Report and Review of the Literature

The Heart Surgery Forum ◽

10.1532/hsf98.20101100 ◽

2011 ◽

Vol 14 (3) ◽

pp. 188 ◽

Cited By ~ 7

Author(s):

Onder Teskin ◽

A. Umit Gullu ◽

Sahin Senay ◽

E. Murat Okten ◽

Cem Alhan

Keyword(s):

Case Report ◽

Aortic Arch ◽

Aortic Coarctation ◽

Interrupted Aortic Arch ◽

Review Of The Literature ◽

Adult Age ◽

Microscopic Pathology ◽

Hallmark Feature ◽

Aortic Interruption

The hallmark feature of aortic interruption that is useful in differentiating it from aortic coarctation is the "complete absence" of continuity between both parts of the interrupted segment. In this study, we reviewed the 28 patients diagnosed with isolated interrupted aortic arch (IAA) who reached adult age (> 20 years), aimed to review the validity of the Celoria-Patton classification in the literature, and reported the first microscopic pathology of the IAA in an adult.

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Surgical Repair for Isolated Aortic Interruption in a Young Adult

The Heart Surgery Forum ◽

10.1532/hsf98.20111192 ◽

2012 ◽

Vol 15 (5) ◽

pp. 289 ◽

Cited By ~ 2

Author(s):

Korhan Erkanli ◽

Burak Onan ◽

Ibrahim Faruk Akt�rk ◽

Ihsan Bakir

Keyword(s):

Cardiopulmonary Bypass ◽

Young Adult ◽

Aortic Arch ◽

Congenital Malformation ◽

Surgical Repair ◽

Interrupted Aortic Arch ◽

Aortic Bypass ◽

Aortic Interruption ◽

Thoracotomy Incision

Interrupted aortic arch (IAA), a rare congenital malformation of the aortic arch, is defined as a loss of luminal continuity between the ascending and descending portions of the aorta. It is rarely diagnosed as an isolated anomaly in adulthood. Surgical repair is feasible through a sternotomy or thoracotomy incision. In this report, we describe the surgical repair of an isolated IAA in a 29-year-old patient by performing an ascending-to-descending aortic bypass via a sternotomy with cardiopulmonary bypass.

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Aortic Arch Reconstruction Using “Autologous Pulmonary Artery Patch” as an Interposition Patch Plasty in Interrupted Aortic Arch and Ventricular Septal Defect

The Thoracic and Cardiovascular Surgeon ◽

10.1055/s-0036-1571575 ◽

2016 ◽

Vol 64 (S 01) ◽

Author(s):

U. Yörüker ◽

C. Yerebakan ◽

H. Elmontaser ◽

K. Valeske ◽

M. Müller ◽

...

Keyword(s):

Ventricular Septal Defect ◽

Pulmonary Artery ◽

Aortic Arch ◽

Septal Defect ◽

Interrupted Aortic Arch ◽

Aortic Arch Reconstruction ◽

Arch Reconstruction ◽

Patch Plasty

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Type B Interrupted Aorta in an Adult Patient

The Heart Surgery Forum ◽

10.1532/hsf98.2013309 ◽

2014 ◽

Vol 17 (2) ◽

pp. 80

Author(s):

Ahmet Ozkara ◽

Mehmet Ezelsoy ◽

Levent Onat ◽

Ilhan Sanisoglu

Keyword(s):

Cardiopulmonary Bypass ◽

Aortic Arch ◽

Collateral Circulation ◽

Neonatal Period ◽

Interrupted Aortic Arch ◽

Complete Loss ◽

Posterolateral Thoracotomy ◽

Type B ◽

Case Presentation ◽

Descending Aorta

Introduction: Interrupted aortic arch is a rare congenital malformation characterized by a complete loss of luminal continuity between the ascending and descending aorta. It is often diagnosed during the neonatal period.Case presentation: We presented a 51-year-old male patient with interrupted aortic arch type B who was treated successfully with posterolateral thoracotomy without using cardiopulmonary bypass.Conclusion: The prognosis for interrupted aortic arch depends on the associated congenital anomalies, but the outcome is usually very poor unless there is surgical treatment. Survival into adulthood depends on the development of collateral circulation.

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Interrupted aortic arch

10.31440/dftb.3630 ◽

2013 ◽

Author(s):

Team DFTB

Keyword(s):

Aortic Arch ◽

Interrupted Aortic Arch

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Conotruncal heart defects and aortic arch anomalies in fetuses with 22q11.2 deletion syndrome

10.21516/2413-1458-2020-19-3-203-209 ◽

2020 ◽

Author(s):

I.V. Novikova, O.M. Khurs, T.V. Demidovich et all

Keyword(s):

Aortic Arch ◽

Heart Defects ◽

22Q11.2 Deletion Syndrome ◽

Ventricular Outflow Tract ◽

Double Outlet Right Ventricle ◽

Interrupted Aortic Arch ◽

Left Ventricular ◽

Deletion Syndrome ◽

22Q11.2 Deletion ◽

Aortic Arch Anomalies

16 second trimester fetuses with 22q11.2 deletion syndrome have been examined at anatomic-pathological investigation. Main cardiovascular diseases were ascending aorta hypoplasia with aortic valve stenosis (n = 6; 37.5%), truncus arteriosus (n = 5; 31.25%), tetralogy of Fallot (n = 3; 18.75%) and double-outlet right ventricle (n = 1; 6.25%). Ventricular septal defect was present in 16 cases. Associated aortic arch anomalies included interrupted aortic arch (n = 9; 56.25%), right aortic arch (n = 6; 37.5%), retroesophageal ring (n = 1; 6.25%) and aberrant right subclavian arteria (n = 5; 31.25%). 5 fetuses had left ventricular outflow tract obstructive lesions with interrupted aortic arch of type B combined with aberrant right subclavian arteria.

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