Donati Fabrizio, Proietti Luca, Burrofato Aaron, Santagada Domenico Alessandro, Tamburrelli Francesco Ciro
Spinal Surgery Department, Catholic University of the Sacred Heart, Rome, Italy.
Childs Nerv Syst. 2016 Aug;32(8):1549-53. doi: 10.1007/s00381-016-3056-8. Epub 2016 Mar 16.
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.
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.
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.
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。
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。
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。