Objective & Hypothesis:In most instances, congenital arteriovenous fistula is only one manifestation of a more widespread abnormality; 60% of patients also have hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber syndrome).
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Key Findings & Data:Among those with congenital pulmonary arteriovenous fistula, the diagnosis is made during infancy in only 15% of patients.
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Conclusion & Impact:We treated our case with lobectomy successfully.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
In most instances, congenital arteriovenous fistula is only one manifestation of a more widespread abnormality; 60% of patients also have hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber syndrome). Among those with congenital pulmonary arteriovenous fistula, the diagnosis is made during infancy in only 15% of patients. We present a case of pulmonary arteriovenous fistula in a newborn and review the literature. This rare condition of newborns can be treated with different surgical procedures. Only 17 cases of newborn pulmonary arteriovenous fistula/have been reported, and only two of those had associated Rendu-Osler-Weber syndrome. The results of surgical procedures were good in most of these cases. We treated our case with lobectomy successfully.
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Cite This Article
OLGUNTÜRK, R., KULA, S., SEZGİN, A., OĞUZ, D., İKİZLER, C., TUNAOĞLU, S. (2022). Pulmonary arteriovenous fistula in the newborn: A case report of Rendu-Osler-Weber syndrome and a review of the literature. Turkish Journal of Pediatrics, Cilt: 43 - Sayı: 4, 332–337. https://ajindex.com/articles/613309