Jsmc-10374

CASE REPORT: POST-MEGASTENT DUODENAL POLYP

Mohammed Omer Mohammed a, Araz Latif Raheem b, and Ali Jabbar Ahmed

College of Medicine, University of Sulaimani, Kurdistan Region, Iraq.

b Gastroenterology and Hepatology Teaching Hospital, Sulaimani, Kurdistan Region, Iraq.

c KBMS board trainee, Gastroenterology and Hepatology Teaching Hospital, Sulaimani, Kurdistan Region, Iraq.

 Submitted: 24/2/2022; Accepted: 15/7/2022; Published: 21/9/2022

DOI Link: https://doi.org/10.17656/jsmc.10374 

Introduction

Most duodenal polyps are non-neoplastic. Instead, they represent regenerative/hyperplastic nodules of foveolar epithelium or Brunner gland proliferation (38%). Other less common polyps include heterotopic (6%) and neoplastic lesions (11%) (1). Adenomas of intestinal type are the most common (89%), followed by adenomatous lesions that present a gastric phenotype: PGAs (8%) and foveolar-type adenomas (3%) (2).

Non-neoplastic duodenal polyps, most of which represent regenerative inflammatory (pseudo) polyps, are predominantly localized in the bulb (80%) (1). The majority are associated with duodenitis, especially in the setting of peptic injury, and are less commonly associated with inflammatory bowel disease or rare conditions such as primary immunodeficiencies. (3). Histologically, non-neoplastic duodenal polyps may resemble gastric hyperplastic polyps and frequently show metaplastic foveolar epithelium with active inflammation and/or erosion, reactive epithelial changes, seamless transition with the surrounding epithelium, and surface maturation. They may also simply be composed of granulation tissue. It is worth underscoring that some of these polyps are neoplastic. Some hyperplastic polyps harbor KRAS and BRAF mutations and tend to show serrated features, similar to their microvascular colonic counterparts (4). Duodenal hyperplastic polyps with KRAS mutation may represent precursor lesions of duodenal traditional serrated adenomas (4). The polypoid heterotopic gastric mucosa is another frequent type of duodenal polyps. As opposed to the peptic injury-induced foveolar metaplasia, lesions of this type also contain clusters of oxyntic glands under the surface of the foveolar epithelium. Duodenal gastric heterotopia is associated with FGPs and PPI therapy.

KEYWORDS

Megastent, Duodenal polyp

References 

1. Jung SH, Chung WC, Kim EJ, et al. Evaluation of non-ampullary duodenal polyps: comparison of non-neoplastic and neoplastic lesions. World J. Gastroenterol. 2010; 16; 5474– 5480.

2. Mitsuishi T, Hamatani S, Hirooka S et al. Clinicopathological characteristics of duodenal epithelial neoplasms: focus on tumors with a gastric mucin phenotype (pyloric gland-type tumors). PLoS ONE 2017; 12; 0174985.

3. Remmele W, Hartmann W, von der Laden U, et al. Three types of duodenal polyps: mucosal cysts, focal foveolar hyperplasia, and hyperplastic polyp originating from islands of the gastric mucosa. Dig. Dis. Sci. 1989; 34; 1468– 1472.

4. Rosty C, Buchanan DD, Walters RJ, et al. Hyperplastic polyp of the duodenum: a report of 9 cases with immunohistochemical and molecular findings. Hum. Pathol. 2011; 42; 1953– 1959.

5. Clinical Issues Committee of the American Society for Metabolic and Bariatric Surgery. Updated position statement on laparoscopic sleeve gastrectomy as a bariatric procedure. Surg Obes Relat Dis 2010; 6: 1–5

6. Casella G, Soricelli E, Rizzello M, et al. Nonsurgical treatment of staple line leaks after laparoscopic sleeve gastrectomy. Obes Surg 2009; 19: 821–826

7. Serra C, Baltasar A, Andreo L, et al. Treatment of gastric leaks with coated self-expanding stents after sleeve gastrectomy. Obes Surg 2007; 17: 866–872

8. Puli SR, Spofford IS, Thompson CC. Use of self-expandable stents to treat bariatric surgery leaks: a systematic review and meta-analysis. Gastrointest Endosc 2012; 75: 287–293

9. http://www.taewoongmedical.com/data/bbsData/16135494902.pdf

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