To tilfælde af det sjældne Cronkhite-Canadas syndrom

Thorbjørn Christensen, Ove B.Schaffalitzky de Muckadell*

*Kontaktforfatter

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Abstract

Cronkhite-Canada syndrome (CCS) is a rare non-heritable condition characterized by gastrointestinal polyposis, dysgeusia, malnutrition, total alopecia and onychodystrophia. Two Danish cases of CCS (an 88-year-old female and a 69-year-old male) presented with signs of malnutrition, dyspepsia, vomiting, dysgeusia and hair loss. An upper endoscopy revealed marked oedema and polyposis in the stomach. Both patients developed colonic adenocarcinomas which were radically operated. Treatment consisted of hyperalimentation, prednisolone and azathioprine. Both patients went into remission - the first patient totally.

Bidragets oversatte titelTwo cases of the rare Cronkhite-Canada syndrome
OriginalsprogDansk
ArtikelnummerV02170155
TidsskriftUgeskrift for Læger
Vol/bind179
Udgave nummer23
Sider (fra-til)2048-2049
ISSN0041-5782
StatusUdgivet - 3. jul. 2017

Emneord

  • Adenocarcinoma/diagnosis
  • Aged
  • Aged, 80 and over
  • Capsule Endoscopy
  • Colorectal Neoplasms/diagnosis
  • Denmark
  • Female
  • Gastroscopy
  • Humans
  • Intestinal Polyposis/diagnosis
  • Male
  • Tomography, X-Ray Computed

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