[Antenatal solitary intestinal fibromatosis]

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Updated: Sep 23, 2026

Chronic Salmonella Infection Induced Intestinal Fibrosis
08:40

Chronic Salmonella Infection Induced Intestinal Fibrosis

Published on: September 22, 2019

Hélène Duval1, Hélène Jouan, Laurence Loeuillet

  • 1Département d'Anatomie et Cytologie Pathologiques CHU Pontchaillou, Rue Henri Le Guilloux, 35000 Rennes.

Annales De Pathologie
|July 5, 2003
PubMed

Insights

Solitary intestinal fibromatosis (SIF) is a rare condition in infants. This case highlights unusual antenatal findings and successful surgical outcomes for this rare intestinal tumor.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Developmental Biology

Background:

  • Solitary intestinal fibromatosis (SIF) is an exceptionally rare mesenchymal tumor affecting the gastrointestinal tract.
  • Limited case reports exist, particularly in neonates and infants, underscoring the rarity of this condition.

Observation:

  • This report details a novel case of SIF presenting with atypical antenatal echographic findings.
  • The diagnosis was confirmed in a 2-month-old infant experiencing intestinal obstruction.

Findings:

  • SIF is a rare cause of intestinal obstruction in infants.
  • Complete surgical excision is curative for SIF, leading to an excellent prognosis.

Implications:

  • Early recognition of SIF, even with unusual antenatal signs, is crucial for timely intervention.
  • This case contributes to the limited literature on SIF, aiding in understanding its presentation and management in early life.

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