Juvenile polyposis of the stomach--a novel cause of hypergastrinemia
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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.
Originalsprog | Engelsk |
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Tidsskrift | Nature Reviews. Gastroenterology & Hepatology |
Vol/bind | 7 |
Udgave nummer | 10 |
Sider (fra-til) | 583-8 |
Antal sider | 6 |
ISSN | 1759-5045 |
DOI | |
Status | Udgivet - 1 okt. 2010 |
ID: 33792540