English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

A 65-year-old man with a history of cerebral infarctionwas referred to our hospital for investigations to find the cause of recurring melena, which he had been experiencing for 2 months. At a previous hospital, he had had an upper gastrointestinal endoscopy and a colonoscopy that failed to show a cause for his bleeding, and an abdominal computed tomography (CT) scan, which detected a strongly enhancing mass in the upper abdomen (● Fig.1). We carried out double-balloon endoscopy using the antegrade approach and found a pedunculated polyp in the jejunum, the surface of which was completely covered with a white coating (● Fig.2). The endoscope could not be inserted beyond this because the mass was occupying the lumen. Endoscopic biopsies revealed inflammatory cells with no evidence of malignancy. The polyp was considered to be the cause of his bleeding, and a segmental resectionof the small intestinewasperformed. Examination of the resected specimen showed that the polyp was 33mm in diameter (● Fig.3), and histology revealed that it was composed of numerous capillaries in an edematous stroma with an inflammatory infiltrate (● Fig.4). These findings were consistent with pyogenic granuloma. After surgery, there was no recurrence of melena over the subsequent 18 months. Pyogenic granulomas usually occur on the skin and in the oral cavity, and rarely in the gastrointestinal tract. Thirteen cases of pyogenic granuloma in the small intestine have been reported [1–3], and most of these were reported to have an irregular shape without surface ulceration and were reddish in color. Because pyogenic granulomas are hemorrhagic tumors, they are usually less than 20mm in diameter (median 13mm). To the best of our knowledge, only one case of a polyp larger than 30mm has been reported [4], and our case is the largest pyogenic granuloma so far reported in the small intestine. Pyogenic granuloma should be considered as a rare cause of obscure gastrointestinal bleeding, although it is difficult to diagnose pyogenic granuloma prior to surgery because of its unusual endoscopic appearance.

Pyogenic granuloma in the small intestine: a rare cause of obscure gastrointestinal bleeding