Intramedullary Extension of Dorsally Located Neurenteric Cyst: A Rarity

A bstract Neurenteric cysts, rare benign tumors of the spinal cord, are foregut duplication cysts occurring as a result of incomplete resorption of the neurenteric canal. A 2-year-girl presented with spastic weakness and sensory loss to pain and temperature of bilateral lower limb without bladder and bowel involvement. On examination, she had spastic paraplegia with exaggerated deep tendon reflex, bilateral extensor planter response, and sensory loss below the L1 dermatome. CEMRI suggested the presence of a C7–T4 intradural extramedullary neurenteric cyst posterior to the spinal cord with intramedullary extension and the association of dysplastic T1–T2 vertebrae with midline fusion anomaly in the T2 vertebra. The patient underwent C6–T3 laminectomy along with partial T4 laminectomy with gross total excision of the cyst. The neurological symptoms improved post-operatively. The histopathological analysis report suggested neurenteric cyst. A diagnosis of neurenteric cyst should be considered even if the lesion is placed dorsal to the spinal cord, especially if associated with midline dysplasia or fusion defect of the vertebral body.

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Publication Details

Journal
Journal of Pediatric Neurosciences
Published
2025-04-01
DOI
https://doi.org/10.4103/jpn.jpn_93_24
Primary Topic
Spinal Dysraphism and Malformations
Type
article
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article

Intramedullary Extension of Dorsally Located Neurenteric Cyst: A Rarity

Journal of Pediatric Neurosciences
Spinal Dysraphism and Malformations
article

Intramedullary Extension of Dorsally Located Neurenteric Cyst: A Rarity

article en

Abstract

A bstract Neurenteric cysts, rare benign tumors of the spinal cord, are foregut duplication cysts occurring as a result of incomplete resorption of the neurenteric canal. A 2-year-girl presented with spastic weakness and sensory loss to pain and temperature of bilateral lower limb without bladder and bowel involvement. On examination, she had spastic paraplegia with exaggerated deep tendon reflex, bilateral extensor planter response, and sensory loss below the L1 dermatome. CEMRI suggested the presence of a C7–T4 intradural extramedullary neurenteric cyst posterior to the spinal cord with intramedullary extension and the association of dysplastic T1–T2 vertebrae with midline fusion anomaly in the T2 vertebra. The patient underwent C6–T3 laminectomy along with partial T4 laminectomy with gross total excision of the cyst. The neurological symptoms improved post-operatively. The histopathological analysis report suggested neurenteric cyst. A diagnosis of neurenteric cyst should be considered even if the lesion is placed dorsal to the spinal cord, especially if associated with midline dysplasia or fusion defect of the vertebral body.

Journal of Pediatric NeurosciencesVol. 20(2)
King George's Medical University (IN)
Openalex Percentile: Top 28%
Spinal Dysraphism and Malformations
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