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Enterogenous cysts (ECs) are rare, benign, congenital ectopic endodermal cysts that only occasionally involve the central nervous system. We presented the diagnosis and treatment of an exceedingly rare case of EC located in the brainstem, which has previously been reported only seven times in pediatric patients. The patient underwent complete surgical resection and experienced no recurrence during the 6-month follow-up.

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Intraspinal enterogenous cysts are rare congenital abnormalities that mainly develop in the spinal canal, more commonly in the cervical and thoracic regions, and rarely in the lumbar spine. We present a case of neurenteric (NE) cyst in the conus medullaris and cauda equina junction at the level of L1 in a patient presenting with a nine-year history of progressive lower limb weakness, paresthesia, and muscle wasting. The patient underwent complete resection of the cyst and had no postoperative complications with marked improvement of paresthesia and some localized pain in the lower back manageable by analgesics.

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Background: Bronchogenic cysts are rare developmental anomalies that belong to the category of congenital enterogenous cysts. They arise from lung buds and are present at birth. The embryonic foregut is their origin.

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Mesenteric cysts are mostly congenital cysts of varied etiology. They occur twice as often in females than in males. They have varied clinical presentations.

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