Abstract
This chapter reviews polyps and polyp-like lesions encountered in the small intestine, which are, in essence, non-neoplastic. First Brunner's gland hyperplasia, Brunner's gland hamartoma and peri-ampullary myo-epithelial hamartoma are discussed. Next Peutz-Jeghers polyp and juvenile polyp are reviewed, including the hereditary autosomal dominant syndromes Peutz-Jeghers syndrome and juvenile polyposis, of which these lesions are the phenotypic hallmarks. Yet another polyposis syndrome with unknown aetiology that is extremely rare, Cronkhite-Canada syndrome, is described and, lastly, pyogenic granuloma, occasionally found in the small intestine, is briefly discussed. Although it may be present as a polyp in the small intestine, inflammatory fibroid polyp is considered in the chapter on stromal tumours of the small intestine.
| Original language | English |
|---|---|
| Title of host publication | Morson and Dawson's Gastrointestinal Pathology, Fifth Edition |
| Publisher | Wiley-Blackwell |
| Pages | 411-421 |
| Number of pages | 11 |
| ISBN (Print) | 9781405199438 |
| DOIs | |
| Publication status | Published - 5 Dec 2012 |
Keywords
- Brunner's gland hamartoma
- Brunner's gland hyperplasia
- Cronkhite-Canada syndrome
- Juvenile polyp
- Juvenile polyposis
- Peri-ampullary myo-epithelial hamartoma
- Peutz-Jeghers polyp
- Peutz-Jeghers syndrome
- Polyp
- Pyogenic granuloma
- Small intestine