Evidence map›Paper›PMID 42578154›Full record

ArticleInternational journal of surgery case reports2026

Acute lower gastrointestinal bleeding from Meckel's diverticulum in a young adult: a case report on surgical management.

Caterina M Nava, Antoine Nobile, François Pugin, Raffaella Sguinzi

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In one paragraph

Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Caterina M NavaDepartment of Surgery, HFR Fribourg Cantonal Hospital, Fribourg, Switzerland.ORCID https://orcid.org/0009-0009-0210-6857
Antoine NobileDepartment of Pathology, Promed Laboratoire Médical SA, Marly, Switzerland.
François PuginDepartment of Surgery, HFR Fribourg Cantonal Hospital, Fribourg, Switzerland.
Raffaella SguinziDepartment of Surgery, HFR Fribourg Cantonal Hospital, Fribourg, Switzerland.ORCID https://orcid.org/0000-0003-0678-3432

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: Meckel's diverticulum (MD) is the most common congenital anomaly of the gastrointestinal tract, yet acute lower gastrointestinal bleeding as a presentation in adults remains uncommon and diagnostically challenging. This case highlights the importance of early surgical decision-making in this setting. Presentation of case: A 20-year-old male with no medical history presented with 2 days of hematochezia. Hemoglobin levels declined over 72 hours. The patient developed hemodynamic instability and episodes of syncope, which were managed on the surgical ward without vasopressor support. Upper and lower endoscopies were unremarkable. Contrast-enhanced computed tomography (CT) identified a blind-ending ileal structure consistent with MD. Laparoscopic exploration confirmed a 7 × 2 cm MD located 140 cm from the ileocecal valve. A 10-cm ileal segment was resected, and a hand-sewn anastomosis was performed. Histopathology confirmed ectopic gastric fundic-type mucosa without ulceration. The postoperative course was complicated by a transient paralytic ileus (Clavien-Dindo grade II), which was managed conservatively, with discharge on day 6. Clinical discussion: MD should be considered in young adults with unexplained hematochezia when standard endoscopy is negative. CT imaging is key in identifying MD. Segmental bowel resection is preferred when ectopic mucosa is suspected. While technetium-99 m pertechnetate scanning may be considered in stable patients with suspected MD, its sensitivity in adults is lower than in children. Conclusion: Surgical resection remains the definitive treatment for symptomatic cases. Prophylactic excision of incidentally discovered MD may be considered in selected patients with risk factors for complications, though this decision should be individualized and weighed against surgical risks.

Identifiers

PMID42578154
PMCPMC13456855

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