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Published on: March 24, 2020
Spinal dysraphism and the Currarino triad
1Department of Neurosurgery, Royal Children's Hospital Brisbane, Brisbane, Queensland, Australia.
This case report details a rare congenital anomaly in a female infant with a lumbosacral lipomyelomeningocele and a pygomelus. The findings suggest an incomplete Currarino
Area of Science:
- Medical case report
- Developmental biology
- Congenital anomalies
Background:
- Lumbosacral lipomyelomeningocele is a complex spinal malformation.
- Currarino's triad involves anorectal malformations, sacral bony abnormalities, and a presacral mass.
- Pygopagus is a rare conjoined twin presentation.
Purpose of the Study:
- To report a unique case of a female infant with multiple congenital anomalies.
- To discuss the association of pygomelus with lipomyelomeningocele and Currarino's triad.
- To contribute to the understanding of rare developmental disorders.
Main Methods:
- Case presentation and clinical description.
- Review of relevant medical literature.
- Analysis of anatomical abnormalities.
Main Results:
- The patient presented with lumbosacral lipomyelomeningocele, a sacral appendage resembling a foot, sacral dysgenesis, anal atresia, and a recto-vaginal fistula.
- Duplication of the right ureter was also noted.
- The constellation of findings is interpreted as a pygomelus associated with lipomyelomeningocele and an incomplete Currarino's triad.
Conclusions:
- This case highlights a rare combination of congenital anomalies.
- The findings expand the spectrum of presentations for lipomyelomeningocele and Currarino's triad.
- Further research into the embryological basis of such complex malformations is warranted.
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