A Taleb*, H Hambli, K Dendane and A Nekhla

Department of Thoracic Surgery, Mohamed NEDIR Hospital, Tizi-Ouzou, Algeria

*Corresponding Author: A Taleb, Department of Thoracic Surgery, Mohamed NEDIR Hospital, Tizi-Ouzou, Algeria.

Received: October 27, 2021; Published: November 18, 2021

Abstract

The evolution of pulmonary arteriovenous malformations (PAVM) over time in children with hereditary hemorrhagic telangiectasia (HHT) is not well defined, this malformation of which cyanosis remains one of the main symptoms requires saving embolization which is the treatment of choice. Surgery is a treatment option that remains very heavy for a population that is often very young.

Keywords: Arteriovenous Malformations; Rendu-Osler; Embolization; Surgery

References

1. Pınar BIÇAKÇIOĞLU., et al. “Surgical treatment of pulmonary arteriovenous malformations”.
2. orpha.net/data/patho/Pro/fr/RenduOsler-FRfrPro236v01.pdf
3. McDonald J and Pyeritz R. “Hereditary Hemorrhagic Telangiectasia”. GeneReviews® Plauchu H, Dupuis-Girod S. Rendu-Osler disease. Orphanet Encyclopedia. Initial Posting (2017).
4. Churton T. “Multiple aneurysm of pulmonary artery”. British Medical Journal 1 (1897): 1223.
5. Claire L Shovlin. “Pulmonary Arteriovenous Malformations”. American Journal of Respiratory and Critical Care Medicine 11 (2014): 1217-1228.

Citation

Citation: A Taleb., et al. “Pulmonary Arteriovenous Fistula: A Clinical Case". Acta Scientific Clinical Case Reports 2.12 (2021): 35-37.

Copyright

Copyright: © 2021 A Taleb., et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.