A rare case of eosinophilic jejunitis: diagnosis and management strategies.
eosinophilic gastroenteritis
eosinophilic gastrointestinal disorders
hypereosinophilic syndrome
Journal
Journal of surgical case reports
ISSN: 2042-8812
Titre abrégé: J Surg Case Rep
Pays: England
ID NLM: 101560169
Informations de publication
Date de publication:
Mar 2024
Mar 2024
Historique:
received:
06
02
2024
accepted:
22
02
2024
medline:
20
3
2024
pubmed:
20
3
2024
entrez:
20
3
2024
Statut:
epublish
Résumé
Eosinophilic gastroenteritis is a rare disease with an unknown cause, which can manifest independently or as part of a hyper-eosinophilic syndrome. The severity of the condition depends on the extent of eosinophilic infiltration and damage to the digestive tract. Diagnosis relies on histological examination, which reveals a significant presence of eosinophilic polymorphonuclear leukocytes in the digestive wall. The authors present a new case of eosinophilic gastroenteritis in a 28-year-old patient who exhibited obstructive symptoms but lacked peripheral eosinophilia. Esophagogastroduodenoscopy showed no abnormalities, but barium transit imaging revealed gastro-duodeno-jejunal dilation upstream of a tight jejunal stenosis. Surgical examination of the affected area confirmed a diffuse and transparietal eosinophilic infiltrate, with no evidence of parasitic or granulomatous lesions. Fortunately, the patient had a swift recovery following surgery. Biopsies conducted at other locations, including the gastric, hepatic, and medullary levels, produced negative results, indicating the localized nature of the condition.
Identifiants
pubmed: 38505336
doi: 10.1093/jscr/rjae157
pii: rjae157
pmc: PMC10948736
doi:
Types de publication
Case Reports
Langues
eng
Pagination
rjae157Informations de copyright
Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2024.
Déclaration de conflit d'intérêts
None declared.