Anaesthetic management of Osler-Weber-Rendu syndrome with coexisting congenital methaemoglobinaemia
Authors:
- 1 October 2005
- journal article
- case report
- Published by Wiley in Acta Anaesthesiologica Scandinavica
- Vol. 49 (9) , 1391-1394
Abstract
A 9-year-old cyanosed child suffering from Osler-Weber-Rendu syndrome with bilateral pulmonary arteriovenous malformations (PAVMs) was posted for cerebral angiography under general anaesthesia. Careful preanaesthetic evaluation led to the diagnosis of coexisting congenital methaemoglobinaemia. There is no previous report of Osler-Weber-Rendu syndrome coexisting with congenital methaemoglobinaemia. This report emphasizes that a second contributory cause of cyanosis must be suspected and meticulously looked for if the symptomatology in a patient cannot be explained by a single established diagnosis. Positive-pressure ventilation was associated with reduction in arterial oxygenation despite an increasing inspired oxygen concentration, which returned to preanaesthetic levels only after extubation and resumption of spontaneous respiration.Keywords
This publication has 6 references indexed in Scilit:
- Pulmonary arteriovenous malformationPostgraduate Medical Journal, 2002
- Severe Oxyhemoglobin Desaturation during Induction of Anesthesia in a Patient with Congenital MethemoglobinemiaAnesthesiology, 2001
- Crofton and Douglas's Respiratory Diseases2000
- Pulse Oximeter Desaturation Due to MethemoglobinemiaAnesthesiology, 1988
- Clinical spectrum of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease)The American Journal of Medicine, 1987
- Hereditary Hemorrhagic Telangiectasia and Pulmonary Arteriovenous FistulaNew England Journal of Medicine, 1959