Isolated true anterior thoracic meningocele associated with severe kyphoscoliosis: a case report.

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2025-05-15 eCollection Date: 2025-01-01 DOI:10.62347/SMEE7102
He-Cheng Zhang, Quan-Shi, Xin Zhang, Wei-Xin Li
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引用次数: 0

Abstract

Introduction: Spinal meningoceles are congenital anomalies characterized by meningeal herniation through vertebral defects, most commonly occurring in the lumbosacral region. Intrathoracic meningoceles are rare and are typically associated with neurofibromatosis type 1 (NF-1). True anterior thoracic meningoceles unassociated with NF-1 represent exceptionally rare clinical entities.

Case summary: This is a retrospective case report. We report a 15-year-old female with severe kyphoscoliosis and a non-NF-1-associated anterior thoracic meningocele who presented with progressive spastic paraparesis. Imaging examinations revealed thoracolumbar scoliosis with 100-degree kyphotic angulation, midline anterior spina bifida at T7, and a well-defined cystic structure exhibiting hypointense T1 and hyperintense T2 signals (measuring 5.7×4.5 cm) anterior to the T7-T8 vertebral bodies. Surgical intervention included posterior spinal laminar decompression, T7 vertebral osteotomy, microscopic dural sac reduction, and stabilization using a pedicle screw system with autologous bone grafting. The patient was discharged without any complications 12 days after surgery, and at the 12-month follow-up, the patient achieved ambulation with a walker and leg brace.

Conclusion: This case underscores the necessity of tailored surgical strategies for anterior thoracic meningoceles complicated by severe spinal deformities. The integration of microsurgical techniques and 3D-printed anatomical modeling may optimize procedural safety and functional outcomes.

孤立性真胸前膜膨出伴严重后凸脊柱侧凸1例。
导语:脊膜膨出是一种先天性异常,其特征是通过椎体缺陷形成脑膜突出,最常见于腰骶区。胸内脑膜膨出是罕见的,通常与1型神经纤维瘤病(NF-1)有关。与NF-1无关的真正胸前脑膜膨出是非常罕见的临床症状。病例总结:这是一份回顾性病例报告。我们报告了一位15岁的女性,她患有严重的脊柱后凸和非nf -1相关的胸前脑膜膨出,并表现为进行性痉挛性截瘫。影像学检查显示胸腰椎侧凸伴100度后凸角,T7中线前脊柱裂,T7- t8椎体前部有明确的囊性结构,表现为T1低信号和T2高信号(测量5.7×4.5 cm)。手术干预包括后路椎板减压、T7椎体截骨、显微硬脑膜囊复位、椎弓根螺钉系统稳定和自体植骨。术后12天,患者无任何并发症出院,随访12个月,患者使用助行器和腿部支架行走。结论:该病例强调了胸前脑膜膨出合并严重脊柱畸形的手术策略的必要性。显微外科技术和3d打印解剖模型的整合可以优化手术安全性和功能结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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552
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