Eosinophilic Myenteric Ganglionitis in a Newborn: Case Report

Eosinophilic myenteric ganglionitis is a rare cause of pseudo-obstructive intestinal syndrome, predominantly reported in children. It is characterized by symptoms that mimic mechanical intestinal obstruction, despite the absence of a demonstrable lesion, and is identified histologically by an eosinophilic myenteric inflammatory process. We report the case of a male newborn presenting with intestinal obstruction found to have intestinal malrotation and histological evidence of colonic wall ganglion cells surrounded by a moderate eosinophilic infiltrate. The patient underwent surgical correction with a protective diverting ileostomy, resulting in progressive clinical improvement. At 18 months of age, follow-up with a contrast enema revealed persistent old contrast medium in the dysfunctional sigmoid rectum, suggesting possible rectal motility impairment. This is the first reported case in the literature of a newborn with intestinal malrotation in the presence of eosinophilic myenteric ganglionitis. The need for comprehensive intestinal wall biopsy for accurate diagnosis is emphasized, highlighting the importance of early diagnosis for proper management and complication prevention. This case underscores the necessity for further research to enhance understanding, diagnosis, and treatment of eosinophilic myenteric ganglionitis.

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Publication Details

Journal
Pediatric and Developmental Pathology
Published
2026-05-19
DOI
https://doi.org/10.1177/10935266261446768
Primary Topic
Eosinophilic Esophagitis
Type
article
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article

Eosinophilic Myenteric Ganglionitis in a Newborn: Case Report

Luz F. Sua, Miguel Conde, Liliana Fernández‐Trujillo, Juan Carlos Bravo
Pediatric and Developmental Pathology
Eosinophilic Esophagitis
article

Eosinophilic Myenteric Ganglionitis in a Newborn: Case Report

Luz F. Sua, Miguel Conde, Liliana Fernández‐Trujillo, Juan Carlos Bravo
article en

Abstract

Eosinophilic myenteric ganglionitis is a rare cause of pseudo-obstructive intestinal syndrome, predominantly reported in children. It is characterized by symptoms that mimic mechanical intestinal obstruction, despite the absence of a demonstrable lesion, and is identified histologically by an eosinophilic myenteric inflammatory process. We report the case of a male newborn presenting with intestinal obstruction found to have intestinal malrotation and histological evidence of colonic wall ganglion cells surrounded by a moderate eosinophilic infiltrate. The patient underwent surgical correction with a protective diverting ileostomy, resulting in progressive clinical improvement. At 18 months of age, follow-up with a contrast enema revealed persistent old contrast medium in the dysfunctional sigmoid rectum, suggesting possible rectal motility impairment. This is the first reported case in the literature of a newborn with intestinal malrotation in the presence of eosinophilic myenteric ganglionitis. The need for comprehensive intestinal wall biopsy for accurate diagnosis is emphasized, highlighting the importance of early diagnosis for proper management and complication prevention. This case underscores the necessity for further research to enhance understanding, diagnosis, and treatment of eosinophilic myenteric ganglionitis.

Pediatric and Developmental Pathology
Fundación Valle del Lili (CO), Icesi University (CO)
Good health and well-being
Openalex Percentile: Top 4%
Eosinophilic Esophagitis
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