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Osler-Weber-Rendu disease: A rare cause of recurrent hemoptysis.

作者信息

Khoja Amir M, Jalan Rahul K, Jain Dheeraj L, Kajale Omkar V

机构信息

Department of Chest Medicine and Thoracic Endoscopy, Ruby Hall Clinic, Pune, Maharashtra, India.

出版信息

Lung India. 2016 May-Jun;33(3):313-6. doi: 10.4103/0970-2113.180878.

Abstract

Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia, is a rare autosomal dominant condition causing systemic fibrovascular dysplasia. It has an incidence of 1-2/100,000. Phenotypic variation is extreme ranging from asymptomatic to severely symptomatic, from cases with no or few mucocutaneous lesions to those with diffuse cutaneous telangiectasia. We discuss a case of Osler-Weber-Rendu disease causing diffuse cutaneous telangiectasia and hemoptysis. The patient presented with complaints of hemoptysis and was extensively examined and investigated before being diagnosed with Osler-Weber-Rendu disease. We successfully managed the patient's hemoptysis by bronchial artery embolization. This case emphasizes the need for careful examination and investigation and to consider such rare diseases when all the common causes of hemoptysis are ruled out. An early and proper diagnosis will lead to more effective management of such a rare disease with few treatment options available.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9577/4857569/cb64accc0ce8/LI-33-313-g001.jpg

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