Evidence map›Paper›PMID 41837004›Full record

ArticleInternational journal of surgery case reports2026

Presumed septic shock from small-bowel obstruction due to a vitellointestinal remnant in a 12-year-old: successful surgical management - a case report.

Mohammad Maraqah, Osama Hazem Jabbarin, Ammer Shawar, Majd Amleh, Roaa Halaykh, Ammar W M Hassouneh

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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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mohammad MaraqahFaculty of Medicine, Hebron University, Hebron, Palestine.ORCID https://orcid.org/0009-0006-2695-0794
Osama Hazem JabbarinFaculty of Medicine, Hebron University, Hebron, Palestine.
Ammer ShawarFaculty of Medicine, Hebron University, Hebron, Palestine.
Majd AmlehFaculty of Medicine, Hebron University, Hebron, Palestine.
Roaa HalaykhFaculty of Medicine, Hebron University, Hebron, Palestine.
Ammar W M HassounehFaculty of Medicine, Hebron University, Hebron, Palestine.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Persistent vitellointestinal (omphalomesenteric) duct (VID) is an uncommon embryologic remnant that typically presents with painless bleeding, umbilical discharge, or mechanical small-bowel obstruction. Presentation with systemic sepsis or septic shock is exceedingly rare. Case presentation: A 12-year-old male presented with 4 days of high-grade fever, progressive abdominal pain, bilious vomiting and hypotension. Imaging demonstrated high-grade small-bowel obstruction with a transition point in the mid-to-distal ileum. After failed conservative management, emergency laparotomy revealed a 1 × 3 cm tubular vitelline remnant with fibrous omental adhesion causing mechanical obstruction. Excision, release of the band, and primary ileal repair were performed. The patient stabilized postoperatively and was discharged on day 5. Discussion: While VID anomalies classically cause localized gastrointestinal complaints, a systemic inflammatory response with circulatory collapse, consistent with septic shock, is uncommon and sparsely reported. Possible pathophysiologic mechanisms include bacterial translocation across ischemic or obstructed bowel, superinfection of a cystic remnant, or a non-infectious overwhelming inflammatory response to necrotic tissue. Because a clinical picture of presumed septic shock can obscure an underlying surgical cause, clinicians should consider VID anomalies in children with compatible abdominal findings. Prompt resuscitation, targeted evaluation for infection, early antimicrobial therapy when indicated, and timely surgical intervention are essential to prevent organ dysfunction. Conclusion: VID can rarely present with systemic inflammatory response with circulatory collapse; recognition of this atypical pattern expedites lifesaving intervention.

Indexed as

omphalomesenteric ductpediatric surgeryshocksmall-bowel obstructionvitellointestinal duct

Identifiers

PMID41837004
PMCPMC12981765

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