Congenital Spinal Lipomatous Malformations. Part 2. Differentiation from Selected Closed Spinal Malformations

Abstract

Background

Congenital spinal lipomatous malformations (spinal lipomas, lipomyeloceles, and lipomyelomeningoceles) are closed neural tube defects over the lower back. Differentiation from some other closed neural tube defects in this region can be problematic for pathologists.

Materials and Methods

This review is based on PubMed searches of the embryology, gross and histopathologic findings, and laboratory reporting requisites for retained medullary spinal cords, coccygeal medullary vestiges and cysts, myelocystoceles, true human vestigial tails, and pseudotails for comparison with congenital spinal lipomatous malformations.

Results

Embryology, imaging, gross and histopathology of these closed neural tube lesions have different but overlapping features compared to congenital spinal lipomatous malformations, requiring context for diagnosis.

Conclusion

The lipomyelocele spectrum and to some degree all of the malformations discussed, even though they may not share gross appearance, anatomic site, surgical approach, or prognosis, require clinical and histopathologic correlation for final diagnosis.

Keywords:

• Medullary spinal cord
• coccygeal medullary vestige
• myelocystocele
• human tail
• pseudotail
• spinal lipoma
• spina bifida
• birth defects

Acknowledgement

The author gratefully acknowledges the assistance of the Rutgers Robert Wood Johnson Medical School Library staff in obtaining many of the articles for this review.

Declaration in interest

The author reports no conflicts of interest. The author alone is responsible for the content and writing of the article.