Case for diagnosis

Boza, Juliana Catucci; Dorn, Timótio Volnei; Oliveira, Fabiana Bazanella de; Bakos, Renato Marchiori

dc.contributor.author	Boza, Juliana Catucci	pt_BR
dc.contributor.author	Dorn, Timótio Volnei	pt_BR
dc.contributor.author	Oliveira, Fabiana Bazanella de	pt_BR
dc.contributor.author	Bakos, Renato Marchiori	pt_BR
dc.date.accessioned	2015-12-24T02:39:28Z	pt_BR
dc.date.issued	2014	pt_BR
dc.identifier.issn	0365-0596	pt_BR
dc.identifier.uri	http://hdl.handle.net/10183/131327	pt_BR
dc.description.abstract	Abstract: The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions. Lesions occur in different organs and can lead to hemorrhage in the lungs, digestive tract and brain. We describe the case of a patient with cutaneous manifestations and severe impairment of the digestive tract. It is important for the dermatologist to recognize this syndrome, since the cutaneous lesions may play a key role in diagnosis.	en
dc.format.mimetype	application/pdf	pt_BR
dc.language.iso	eng	pt_BR
dc.relation.ispartof	Anais brasileiros de dermatologia. Rio de Janeiro. Vol. 89, n. 6 (2014), p. 999-1001.	pt_BR
dc.rights	Open Access	en
dc.subject	Diagnóstico	pt_BR
dc.subject	Diagnosis	en
dc.subject	Epistaxe	pt_BR
dc.subject	Epistaxis	en
dc.subject	Telangiectasia	en
dc.subject	Telangiectasia	pt_BR
dc.subject	Telangiectasia hemorrágica hereditária	pt_BR
dc.subject	Hereditary hemorrhagic	en
dc.subject	Telangiectasis	en
dc.title	Case for diagnosis	pt_BR
dc.type	Artigo de periódico	pt_BR
dc.identifier.nrb	000979376	pt_BR
dc.type.origin	Nacional	pt_BR

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