Suppr超能文献

原发性良性腹膜后及椎管内哑铃形囊性畸胎瘤:病例报告

"Primary" benign retroperitoneal and intraspinal dumbbell-shaped cystic teratoma: case report.

作者信息

Kao Ting-Hsien, Shen Chiung-Chyi, Chen Chi-Chang, Kwan Pao-Hsiang

机构信息

Department of Neurosurgery, Taichung Veterans General Hospital, Taichung, Taiwan, ROC.

出版信息

Spine (Phila Pa 1976). 2005 Aug 1;30(15):E439-43. doi: 10.1097/01.brs.0000172227.46437.63.

Abstract

STUDY DESIGN

A case of unusual dumbbell-shaped cystic teratoma is presented.

OBJECTIVES

To investigate and describe an unusual case of retroperitoneal cystic teratoma with spinal invasion in an adult. The image findings, minimally invasive surgical procedures, and clinical outcome were discussed, and the literature was reviewed.

SUMMARY OF BACKGROUND DATA

Primary benign cystic teratomas of the retroperitoneum are rare. Extension of these lesions into the spinal canal is more rare. In this report, by presenting a case of cystic teratoma with such extension, the origin of the tumor, and the value of computerized tomography and magnetic resonance imaging (MRI) in the preoperative diagnosis and surgical approach for the extended lesion are discussed.

METHODS

The patient was a 24-year-old female who had had low back pain with bilateral sciatica for 2 months. Preoperative computerized tomography and MRI of the thoracic and lumbar spines showed a dumbbell-shaped tumor, with the solid part residing in the right retroperitoneum near the neuroforamen of the L2-L3 spines and the cystic part extending into the spinal canal. By performing right L2-L4 hemilaminectomies with a mini retroperitoneal approach, the tumor was removed en bloc in one stage.

RESULTS

Diagnosis of cystic teratoma was confirmed by pathologic examination. The patient recovered well without any neurologic deficits, and recurrence of tumor has not been found for 9 years postoperatively.

CONCLUSIONS

Total surgical removal of tumor is an ideal treatment for retroperitoneal and intraspinal dumbbell-shaped cystic teratoma. MRI displays the precise location, morphology, and adjacent structures of the tumor, which provide for better preoperative planning and more complete removal of tumor with less neurologic damage.

摘要

研究设计

报告一例罕见的哑铃形囊性畸胎瘤病例。

目的

研究并描述一例成人腹膜后囊性畸胎瘤侵犯脊柱的罕见病例。讨论其影像表现、微创外科手术及临床结果,并复习相关文献。

背景资料总结

原发性腹膜后良性囊性畸胎瘤罕见。这些病变延伸至椎管更为罕见。在本报告中,通过呈现一例有此类延伸的囊性畸胎瘤病例,讨论了肿瘤的起源以及计算机断层扫描和磁共振成像(MRI)在该扩展性病变术前诊断及手术入路中的价值。

方法

患者为一名24岁女性,下腰痛伴双侧坐骨神经痛2个月。胸腰椎术前计算机断层扫描和MRI显示一个哑铃形肿瘤,实性部分位于L2 - L3棘突神经孔附近的右侧腹膜后,囊性部分延伸至椎管内。通过采用迷你腹膜后入路行右侧L2 - L4半椎板切除术,一期完整切除肿瘤。

结果

病理检查确诊为囊性畸胎瘤。患者恢复良好,无任何神经功能缺损,术后9年未发现肿瘤复发。

结论

完整手术切除肿瘤是腹膜后及椎管内哑铃形囊性畸胎瘤的理想治疗方法。MRI可显示肿瘤的精确位置、形态及相邻结构,有助于更好地进行术前规划,更完整地切除肿瘤且减少神经损伤。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验