A rare case of spinal rudimentary meningocoele mimicking a spinal dermoid cyst in a cat

Abstract This report describes a rare case of a rudimentary meningocoele in a 1‐year‐old Scottish Fold cat. The presentation included multiple congenital abnormalities of the thoracolumbar vertebrae and sacrum, as well as a spastic contracture of the right pelvic limb. Advanced imaging, including plain computed tomography and fistulography, confirmed the diagnosis and aided in planning an L6 to S2 dorsal laminectomy for lesion excision. Surgery was performed to prevent complications such as infection and the progression of neurological deficits. Exploration of the lesion revealed a bifid cauda equina. The immediate postoperative outcome was satisfactory. The owner reported an excellent outcome at the 6‐month follow‐up. This rare case highlights that proliferation of meningothelial elements can be present in the cutaneous and subcutaneous tissues, that spinal dysraphism anomalies are often multiple rather than isolated, and that there is significant variability in their presentation. It also provides detailed insights into their diagnosis and surgical management.

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Publication Details

Journal
Veterinary Record Case Reports
Published
2025-10-25
DOI
https://doi.org/10.1002/vrc2.70243
Primary Topic
Spinal Dysraphism and Malformations
Type
article
Field-Weighted Citation Impact
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article

A rare case of spinal rudimentary meningocoele mimicking a spinal dermoid cyst in a cat

Marilène Paquet, Estelle Marchal, Audrey Albert, Barnabé Courzereaux et al.
Veterinary Record Case Reports
Spinal Dysraphism and Malformations
article

A rare case of spinal rudimentary meningocoele mimicking a spinal dermoid cyst in a cat

Marilène Paquet, Estelle Marchal, Audrey Albert, Barnabé Courzereaux, Alex Terreros
article en

Abstract

Abstract This report describes a rare case of a rudimentary meningocoele in a 1‐year‐old Scottish Fold cat. The presentation included multiple congenital abnormalities of the thoracolumbar vertebrae and sacrum, as well as a spastic contracture of the right pelvic limb. Advanced imaging, including plain computed tomography and fistulography, confirmed the diagnosis and aided in planning an L6 to S2 dorsal laminectomy for lesion excision. Surgery was performed to prevent complications such as infection and the progression of neurological deficits. Exploration of the lesion revealed a bifid cauda equina. The immediate postoperative outcome was satisfactory. The owner reported an excellent outcome at the 6‐month follow‐up. This rare case highlights that proliferation of meningothelial elements can be present in the cutaneous and subcutaneous tissues, that spinal dysraphism anomalies are often multiple rather than isolated, and that there is significant variability in their presentation. It also provides detailed insights into their diagnosis and surgical management.

Veterinary Record Case ReportsVol. 13(4)
Cegep de Saint Hyacinthe (CA), CTT Group (Canada) (CA), Université de Montréal (CA)
Openalex Percentile: Top 59%
Spinal Dysraphism and Malformations
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