XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?.

Authors

  • António Amador Serviço de Pediatria, Hospital Dr. Manoel Constâncio, Abrantes.
  • Isabel Martins
  • Rosário Massa
  • J Oliveira Santos

DOI:

https://doi.org/10.20344/amp.888

Abstract

The XYY male has characteristicaly tall stature, behavior problems and speech delay. There may may be an association with nephro-urologic malformations but cardiovascular anomalies are usually not present.It is reported a case of a boy with a 47 XYY karyotype with persistent respiratory distress and swallowing difficulties since two months old. On diagnosis workup the fiberoptic bronchoscopy showed a significant pulsatil tracheal obstruction at its right lateral wall and the magnetic resonance imaging of the mediastinum comproved the presence of a vascular ring (right aortic arch with left ligamentum arteriosum). The patient was submitted to surgery with improvment in the respiratory symptoms.The XYY male is a sex chromosomal abnormality that usually is not associated with cardiovascular malformations. A vascular ring presents with persistent respiratory distress and feeding difficulties; the begining and severity of the symptoms varies with the type of vascular ring. The main procedure to be requested is the fiberoptic bronchoscopy and the best image study is the magnetic resonance imaging of the mediastinum.

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How to Cite

1.
Amador A, Martins I, Massa R, Oliveira Santos J. XYY male with right aortic arch and ligamentum arteriosum: a fortuitus association?. Acta Med Port [Internet]. 2008 Feb. 13 [cited 2024 Nov. 24];20(6):575-80. Available from: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/888

Issue

Section

Arquivo Histórico