Literature DB >> 25628855

A 3 years old girl with Dysphagia.

Reza Khajeh1, MohamadHasan Nemati1.   

Abstract

Entities:  

Year:  2015        PMID: 25628855      PMCID: PMC4293803     

Source DB:  PubMed          Journal:  Middle East J Dig Dis        ISSN: 2008-5230


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We report the case of a three-year-old girl who complained from dysphagia and post-prandial vomiting since she was 6 months old. Several diagnostic work-ups were performed for her problem. Upper GI endoscopy was normal but barium swallow revealed an external pressure effect over upper part of the esophagus (figure 1) and the CT angiography of thoracic aorta showed that this external pressure effect was due to a vascular anomaly in the aberrant branching of subclavian artery in the right side directly from aortic arch transmitting from the posterior aspect of the esophagus (figure 2). So the patient underwent elective operation and thorough right posterolateral thoracotomy from 5th intercostal space, right subclavian artery was divided from its origin to aorta and end to side anastomosis was made to proximal part of right carotid artery. Site of previous origin on aorta also was closed. After 5 days the patient was discharged from the hospital with good condition without any complication.
Fig. 1
Fig. 2
Barium swallow shows narrowing in proximal part of esophagus. CT angiography reveals aberrant Right subclavian artery. Vascular anomalies are rare causes of dysphagia. Most of them are asymptomatic but may rarely have compressing effects on trachea or esophagus and cause dyspnea, recurrent pneumonia or dysphagia.[1] Aberrant origin of the subclavian artery was fist described by Hunted in 1735. In 1794 Bayford first reported a rare condition in which an anomalous right subclavian artery compressed the esophagus and caused symptoms of dysphagia; he called it dysphagia lusoria. However, until 1936, when Kommerell encountered an aortic diverticulum while performing a radiological examination of the stomach, the diagnosis of an aberrant subclavian artery had been made at postmortem examination only. Anomalous right subclavian artery occurs in approximately 0.5% to 1.0% of the population and it is caused by obliteration of the right fourth aortic arch during early embryologic development.[2] The current recommendation for treatment of aberrant right subclavian artery is by surgical division of the anomalous vessel at its origin and revascularization of the right upper extremity by direct end to-side anastomosis to the ascending aortic arch.[3]

What is your Diagnosis?

Diagnosis: Aberrant right subclavian artery or dysphagia lusoria

CONFLICT OF INTEREST

The authors declare no conflict of interest related to this work.
  3 in total

1.  Dysphagia lusoria caused by a complex congenital vascular abnormality.

Authors:  G Martín-Sánchez; M Aller; J L Hernández
Journal:  QJM       Date:  2011-03-11

2.  Dysphagia lusoria caused by aberrant right subclavian artery, Kommerell's diverticulum, legamentum ring, right descending aorta, and absent left pulmonary artery: a report of a unique vascular congenital disease undetected until adulthood and a review of the literature.

Authors:  W Hassan; A Al Omrani; M Neimatallah; F Al Fadley; Z Al Halees
Journal:  Pediatr Cardiol       Date:  2005 Nov-Dec       Impact factor: 1.655

3.  Adult dysphagia lusoria. Treatment by arterial division and reestablishment of vascular continuity.

Authors:  K J Karlson; F W Heiss; F H Ellis
Journal:  Chest       Date:  1985-05       Impact factor: 9.410

  3 in total

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