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Updated: May 6, 2026

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Intraoperative Ultrasound in Spinal Surgery
Published on: August 17, 2022
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Unusual spinal dysraphic lesions
Jose Roberto Tude Melo1, Pollyana Pacheco, Luiz Eduardo Wanderley
1Pediatric Neurosurgical Unit, Hospital Pediátrico Martagão Gesteira, Rua Jose Duarte 114, Tororó, 40000 Salvador, BA, Brazil.
Case Reports in Pediatrics
|November 7, 2013
Summary
This study examines rare congenital conditions: human tail and multiple spinal dysraphism. Microsurgical resection of these spinal malformations was successfully performed without complications.
Area of Science:
- Pediatric Surgery
- Developmental Biology
- Neurology
Background:
- Human tail and multiple spinal dysraphism are rare congenital anomalies.
- Spinal dysraphisms are typically isolated, with multiple occurrences being exceptionally uncommon.
- The study focuses on unusual presentations of these conditions.
Purpose of the Study:
- To describe unusual cases of human tail and multiple spinal dysraphism.
- To review the literature on the diagnosis and treatment of these conditions.
- To evaluate the efficacy and safety of microsurgical techniques for resection.
Main Methods:
- Case series describing two instances of human tail and one of multiple thoracic myelomeningocele.
- Comprehensive literature review on diagnosis and management strategies.
- Application of microsurgical techniques for lesion exploration and resection.
Main Results:
- Two cases of human tail and one case of multiple thoracic myelomeningocele were identified.
- Microsurgical exploration allowed for detailed assessment of the lesions.
- Successful resection of the congenital malformations was achieved with no reported morbidity.
Conclusions:
- Microsurgical techniques are effective for the exploration and resection of rare spinal malformations like human tail and multiple spinal dysraphism.
- Prompt diagnosis and surgical intervention can lead to favorable outcomes without complications.
- Further research into the etiology and management of these rare conditions is warranted.
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