Morbus Osler diagnosticeret hos 16-årig i forbindelse med en trafikulykke

Pradeesh Sivapalan, Ann Kathrin Demény, Merete Almind, Anette Drøhse Kjeldsen

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Resumé

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterized by vascular dysplasia and haemorrhage. It is manifested by mucocutaneous telangiec-tases and arteriovenous malformations in organs such as lungs, liver and brain. We present a case of HHT. A 16-year-old patient with a history of recurrent epistaxis was admitted to the local hospital with chest pain and desaturation. A CT scan revealed pulmonary arteriovenous malformations.

OriginalsprogDansk
TidsskriftUgeskrift for Laeger
Vol/bind176
Udgave nummer8A
Sider (fra-til)2-3
ISSN0041-5782
StatusUdgivet - 17. feb. 2014

Fingeraftryk

Traffic Accidents
Lung
Epistaxis
Liver

Citer dette

Sivapalan, Pradeesh ; Demény, Ann Kathrin ; Almind, Merete ; Kjeldsen, Anette Drøhse. / Morbus Osler diagnosticeret hos 16-årig i forbindelse med en trafikulykke. I: Ugeskrift for Laeger. 2014 ; Bind 176, Nr. 8A. s. 2-3.
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abstract = "Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterized by vascular dysplasia and haemorrhage. It is manifested by mucocutaneous telangiec-tases and arteriovenous malformations in organs such as lungs, liver and brain. We present a case of HHT. A 16-year-old patient with a history of recurrent epistaxis was admitted to the local hospital with chest pain and desaturation. A CT scan revealed pulmonary arteriovenous malformations.",
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Sivapalan, P, Demény, AK, Almind, M & Kjeldsen, AD 2014, 'Morbus Osler diagnosticeret hos 16-årig i forbindelse med en trafikulykke', Ugeskrift for Laeger, bind 176, nr. 8A, s. 2-3.

Morbus Osler diagnosticeret hos 16-årig i forbindelse med en trafikulykke. / Sivapalan, Pradeesh; Demény, Ann Kathrin; Almind, Merete; Kjeldsen, Anette Drøhse.

I: Ugeskrift for Laeger, Bind 176, Nr. 8A, 17.02.2014, s. 2-3.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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AB - Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterized by vascular dysplasia and haemorrhage. It is manifested by mucocutaneous telangiec-tases and arteriovenous malformations in organs such as lungs, liver and brain. We present a case of HHT. A 16-year-old patient with a history of recurrent epistaxis was admitted to the local hospital with chest pain and desaturation. A CT scan revealed pulmonary arteriovenous malformations.

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