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一名儿科患者腰椎的椎管内硬膜外良性纤维组织细胞瘤。病例报告及文献综述。

Intraspinal extradural benign fibrous histiocytoma of the lumbar spine in a pediatric patient. Case report and literature review.

作者信息

Donati Fabrizio, Proietti Luca, Burrofato Aaron, Santagada Domenico Alessandro, Tamburrelli Francesco Ciro

机构信息

Spinal Surgery Department, Catholic University of the Sacred Heart, Rome, Italy.

出版信息

Childs Nerv Syst. 2016 Aug;32(8):1549-53. doi: 10.1007/s00381-016-3056-8. Epub 2016 Mar 16.

Abstract

INTRODUCTION

Benign fibrous histiocytoma (BFH) is a rare skeletal tumor. Spinal localizations have been previously described in 17 cases, and this is the first report of BFH occurring at the lumbar spine in a pediatric patient.

CASE REPORT

A 13-year-old male complained lower limb motor and sensory impairment with severe claudication and urination disorders. A huge intraspinal, extradural mass at L4-L5 level, clearly evident on a preoperative MRI, caused dislocation and severe compression of the cauda equina nerve roots. After a biopsy, confirming BFH, a tumor resection and L4-S1 vertebral arthrodesis was carried out. At 1 year follow-up, no recurrence was detached on postoperative MRI, with complete neurological recovery.

DISCUSSION AND CONCLUSION

Review of the literature is discussed. Histological examination is mandatory for a correct diagnosis and plan of treatment. None of the pediatric patients treated for BFH have ever shown local relapse.

摘要

引言

良性纤维组织细胞瘤(BFH)是一种罕见的骨骼肿瘤。先前已有17例关于脊柱部位的报道,而这是首例关于小儿患者腰椎发生BFH的报告。

病例报告

一名13岁男性患者,主诉下肢运动和感觉障碍,伴有严重跛行和排尿障碍。术前MRI清晰显示,L4-L5水平有一个巨大的椎管内硬膜外肿块,导致马尾神经根脱位和严重受压。活检确诊为BFH后,进行了肿瘤切除及L4-S1椎体融合术。术后1年随访,MRI显示无复发,神经功能完全恢复。

讨论与结论

对相关文献进行了讨论。组织学检查对于正确诊断和治疗方案规划至关重要。接受BFH治疗的小儿患者均未出现局部复发。

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