An uncommon cause of multiple pulmonary nodules; hereditary hemorrhagic telangiectasia

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dc.authoridGonlugur, Ugur/0000-0001-8720-2788
dc.contributor.authorKosar, Sule
dc.contributor.authorKizildag, Betul
dc.contributor.authorCanan, Arzu
dc.contributor.authorKaratag, Ozan
dc.contributor.authorGonlugur, Ugur
dc.contributor.authorSariyildirim, Abdullah
dc.date.accessioned2025-01-27T20:14:31Z
dc.date.available2025-01-27T20:14:31Z
dc.date.issued2016
dc.departmentÇanakkale Onsekiz Mart Üniversitesi
dc.description.abstractHereditary hemorrhagic telangiectasia ( HHT), or Rendu-Osler-Weber syndrome ( ROWS) is a very rare hereditary disease. The diagnosis is based on the clinical findings such as recurrent epistaxis, telangiectases, visceral arteriovenous malformations (AVMs) and family history. AVMs are found in the liver, lung or brain and could mimick the masses of these organs. Radiologic evaluation plays a critical role during diagnostic and therapeutic management of ROWS. Hence, radiologists should be aware of the diagnosis of HHT in the patients with AVMs, history of epistaxis and family history. We report a patient with multiple pulmonary AVMs secondary to HHT who has referred to our interventional radiology department for computed tomography guided transthorasic lung biopsy procedure with suspicious of malignancy.
dc.identifier.doi10.5578/tt.8900
dc.identifier.endpage76
dc.identifier.issn0494-1373
dc.identifier.issue1
dc.identifier.pmid27266289
dc.identifier.scopus2-s2.0-84969262541
dc.identifier.scopusqualityQ3
dc.identifier.startpage73
dc.identifier.urihttps://doi.org/10.5578/tt.8900
dc.identifier.urihttps://hdl.handle.net/20.500.12428/21121
dc.identifier.volume64
dc.identifier.wosWOS:000386262800011
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTurkish Assoc Tuberculosis & Thorax
dc.relation.ispartofTuberkuloz Ve Torak-Tuberculosis and Thorax
dc.relation.publicationcategoryinfo:eu-repo/semantics/openAccess
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20250125
dc.subjectHereditary hemorrhagic telangiectasia
dc.subjectpulmonary arteriovenous malformations
dc.subjectcomputed tomography
dc.titleAn uncommon cause of multiple pulmonary nodules; hereditary hemorrhagic telangiectasia
dc.title.alternativeÇoklu pulmoner nodülün nadir sebebi; herediter hemorajik telenjiektazi
dc.typeArticle

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