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Inverted Meckel’s diverticulum diagnosed using capsule endoscopy: A case report

BACKGROUND: Meckel’s diverticulum is a common asymptomatic congenital gastrointestinal anomaly. However, its presentation as an inverted Meckel's diverticulum is a rare complication, of which few cases have been reported in the literature. CASE SUMMARY: Here, we report the case of a 33-year-old...

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Detalles Bibliográficos
Autores principales: El Hajra Martínez, Ismael, Calvo, Marta, Martínez-Porras, José Luis, Gomez-Pimpollo Garcia, Lucia, Rodriguez, Jose L, Leon, Carmen, Calleja Panero, José Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476338/
https://www.ncbi.nlm.nih.gov/pubmed/34629826
http://dx.doi.org/10.3748/wjg.v27.i36.6154
Descripción
Sumario:BACKGROUND: Meckel’s diverticulum is a common asymptomatic congenital gastrointestinal anomaly. However, its presentation as an inverted Meckel's diverticulum is a rare complication, of which few cases have been reported in the literature. CASE SUMMARY: Here, we report the case of a 33-year-old man with iron deficiency anemia without manifestation of gastrointestinal bleeding. An upper gastrointestinal endoscopy and total colonoscopy were performed, but no abnormalities were found within the observed area. Finally, a capsule endoscopy was performed and offered us a clue to subsequently confirm the diagnosis of inverted Meckel's diverticulum via computed tomography scan. Laparoscopic intestinal resection surgery was performed. The final pathology report described a Meckel’s diverticulum. CONCLUSION: Since inverted Meckel's diverticulum is an uncommon disease and its clinical presentation is not specific, it may go undetected by capsule endoscopy. Successful diagnosis and treatment of this disease requires a high index of clinical suspicion.