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Hereditaert angioödem - en udfordrende diagnose
Engelsk titel: Hereditary angioedema - diagnostic problems Läs online Författare: Bach RO ; Bygum A Språk: Dan Antal referenser: 5 Dokumenttyp: Fallbeskrivning UI-nummer: 09021958

Tidskrift

Ugeskrift for Laeger 2009;171(5)333-4 ISSN 0041-5782 E-ISSN 1603-6824 KIBs bestånd av denna tidskrift Denna tidskrift är expertgranskad (Peer-Reviewed)

Sammanfattning

Hereditary angioedema (HAE) is a rare, but potentially life-threatening condition, clinically characterized by recurrent and self-limiting episodes of swelling which affect the skin, gastrointestinal tract and upper airways, and are caused by a lack of complement-C1-inhibitor (C1-INH). Within the past ten years, two Danish HAE patients have died from laryngeal oedema. We report two cases that illustrate symptoms and differential diagnostic problems posed by this disease, and the importance of an effective treatment strategy.