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

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

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

Translated title of the contribution: Hereditary haemorrhagic telangiectasia diagnosed in connection with a traffic accident

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

Department of Respiratory Medicine

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.

Translated title of the contribution	Hereditary haemorrhagic telangiectasia diagnosed in connection with a traffic accident
Original language	Danish
Journal	Ugeskrift for Laeger
Volume	176
Issue number	8A
Pages (from-to)	V10130614
ISSN	0041-5782
Publication status	Published - 17 Feb 2014

Keywords

Case Reports
Journal Article

Cite this

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title = "Morbus Osler diagnosticeret hos 16-{\aa}rig i forbindelse med en trafikulykke",

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.",

keywords = "Accidents, Traffic, Adolescent, Arteriovenous Malformations, Humans, Male, Pulmonary Artery, Pulmonary Veins, Radiography, Telangiectasia, Hereditary Hemorrhagic, Case Reports, Journal Article",

author = "Pradeesh Sivapalan and Dem{\'e}ny, \{Ann Kathrin\} and Merete Almind and Kjeldsen, \{Anette Dr{\o}hse\}",

year = "2014",

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language = "Dansk",

volume = "176",

pages = "V10130614",

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TY - JOUR

T1 - Morbus Osler diagnosticeret hos 16-årig i forbindelse med en trafikulykke

AU - Sivapalan, Pradeesh

AU - Demény, Ann Kathrin

AU - Almind, Merete

AU - Kjeldsen, Anette Drøhse

PY - 2014/2/17

Y1 - 2014/2/17

N2 - 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.

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.

KW - Accidents, Traffic

KW - Adolescent

KW - Arteriovenous Malformations

KW - Humans

KW - Male

KW - Pulmonary Artery

KW - Pulmonary Veins

KW - Radiography

KW - Telangiectasia, Hereditary Hemorrhagic

KW - Case Reports

KW - Journal Article

UR - https://www.scopus.com/pages/publications/84989167878

M3 - Tidsskriftartikel

C2 - 25350308

SN - 0041-5782

VL - 176

SP - V10130614

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

IS - 8A

ER -

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

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