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Pregled bibliografske jedinice broj: 1229661

Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations and a cerebral abscess as a complication: A case report

Krivdić Dupan, Zdravka; Guljaš, Silva; Periša, Vlatka; Laslo, Dorian; Salha, Tamer, Koruga, Nenad
Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations and a cerebral abscess as a complication: A case report // Journal of Case Reports and Images in Surgery, 8 (2022), 2; 4-8 doi:10.5348/100105Z12ZD2022CR (međunarodna recenzija, članak, stručni)

CROSBI ID: 1229661 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations and a cerebral abscess as a complication: A case report

Autori
Krivdić Dupan, Zdravka ; Guljaš, Silva ; Periša, Vlatka ; Laslo, Dorian ; Salha, Tamer, Koruga, Nenad

Izvornik
Journal of Case Reports and Images in Surgery (0976-3198) 8 (2022), 2; 4-8

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, stručni

Ključne riječi
Arteriovenous malformations, Brain abscess, Hereditary hemorrhagic telangiectasia, Hypoxemia, Polycythemia How to ci

Sažetak
Hereditary hemorrhagic telangiectasia (HHT) also known as Osler–Weber–Rendu syndrome is a relatively common, under-recognized autosomaldominant disorder that results from multisystem vascular dysplasia. It is characterized by telangiectasis and arteriovenous malformations of skin, mucosa, andviscera.

Izvorni jezik
Engleski



POVEZANOST RADA

Ustanove:
Klinički bolnički centar Osijek,
Medicinski fakultet, Osijek,
Fakultet za dentalnu medicinu i zdravstvo, Osijek

Profili:

Avatar Url Nenad Koruga (autor)

Avatar Url Vlatka Periša (autor)

Avatar Url Tamer Salha (autor)

Avatar Url Dorian Laslo (autor)

Avatar Url Silva Guljaš (autor)

Poveznice na cjeloviti tekst rada:

Pristup cjelovitom tekstu rada doi www.ijcrisurgery.com www.ijcrisurgery.com

Citiraj ovu publikaciju:

Krivdić Dupan, Zdravka; Guljaš, Silva; Periša, Vlatka; Laslo, Dorian; Salha, Tamer, Koruga, Nenad
Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations and a cerebral abscess as a complication: A case report // Journal of Case Reports and Images in Surgery, 8 (2022), 2; 4-8 doi:10.5348/100105Z12ZD2022CR (međunarodna recenzija, članak, stručni)
Krivdić Dupan, Z., Guljaš, S., Periša, V., Laslo, D. & Salha, Tamer, Koruga, Nenad (2022) Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations and a cerebral abscess as a complication: A case report. Journal of Case Reports and Images in Surgery, 8 (2), 4-8 doi:10.5348/100105Z12ZD2022CR.
@article{article, author = {Krivdi\'{c} Dupan, Zdravka and Gulja\v{s}, Silva and Peri\v{s}a, Vlatka and Laslo, Dorian}, year = {2022}, pages = {4-8}, DOI = {10.5348/100105Z12ZD2022CR}, keywords = {Arteriovenous malformations, Brain abscess, Hereditary hemorrhagic telangiectasia, Hypoxemia, Polycythemia How to ci}, journal = {Journal of Case Reports and Images in Surgery}, doi = {10.5348/100105Z12ZD2022CR}, volume = {8}, number = {2}, issn = {0976-3198}, title = {Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations and a cerebral abscess as a complication: A case report}, keyword = {Arteriovenous malformations, Brain abscess, Hereditary hemorrhagic telangiectasia, Hypoxemia, Polycythemia How to ci} }
@article{article, author = {Krivdi\'{c} Dupan, Zdravka and Gulja\v{s}, Silva and Peri\v{s}a, Vlatka and Laslo, Dorian}, year = {2022}, pages = {4-8}, DOI = {10.5348/100105Z12ZD2022CR}, keywords = {Arteriovenous malformations, Brain abscess, Hereditary hemorrhagic telangiectasia, Hypoxemia, Polycythemia How to ci}, journal = {Journal of Case Reports and Images in Surgery}, doi = {10.5348/100105Z12ZD2022CR}, volume = {8}, number = {2}, issn = {0976-3198}, title = {Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations and a cerebral abscess as a complication: A case report}, keyword = {Arteriovenous malformations, Brain abscess, Hereditary hemorrhagic telangiectasia, Hypoxemia, Polycythemia How to ci} }

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