Juvenile polyposis of the stomach--a novel cause of hypergastrinemia

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

A 38-year-old female presented with a 3-year history of postprandial abdominal pain, refractory nausea, vomiting and hematemesis. She appeared malnourished and her symptoms were refractory to previous treatment with acid-suppressive drugs, prokinetics and antiemetics. Her medical history was significant for a diagnosis of juvenile polyposis syndrome at the age of 14 resulting in a transverse colectomy, and a diagnosis of Crohn's disease in her residual colon at the age of 35 resulting in a total colectomy.
OriginalsprogEngelsk
TidsskriftNature Reviews. Gastroenterology & Hepatology
Vol/bind7
Udgave nummer10
Sider (fra-til)583-8
Antal sider6
ISSN1759-5045
DOI
StatusUdgivet - 1 okt. 2010

ID: 33792540