George Washington University School of Medicine and Health Sciences; and
J Neurosurg Spine. 2014 Aug;21(2):275-8. doi: 10.3171/2014.3.SPINE13651. Epub 2014 May 2.
Spindle cell hemangioendothelioma is a rare benign vascular tumor that is not known to involve the sacrum. The authors describe the case of a 31-year-old woman presenting with low-back and radicular pain without weakness or bowel or bladder dysfunction. Admission CT and MRI studies revealed a large S1-3 lytic sacral lesion. The patient initially underwent a nondiagnostic percutaneous biopsy. She subsequently underwent an open biopsy, during which the lesion was found to be highly vascular. Histological investigation revealed a vasoformative lesion consistent with spindle cell hemangioendothelioma. Preoperative embolization followed by resection via intralesional currettage resulted in resolution of symptoms up to 9 months postintervention. Despite the authors' recommendation, the patient became pregnant at that time and requested no additional follow-up imaging. The authors present the first reported case of a spindle cell hemangioendothelioma of the sacrum and review the current literature.
梭形细胞血管内皮细胞瘤是一种罕见的良性血管肿瘤,据知不涉及骶骨。作者描述了一位 31 岁女性的病例,她表现为下腰痛和神经根痛,无无力或肠或膀胱功能障碍。入院 CT 和 MRI 研究显示 S1-3 溶骨性骶骨病变大。患者最初接受了非诊断性经皮活检。随后她进行了开放性活检,在此过程中发现病变具有高度血管性。组织学研究显示符合梭形细胞血管内皮细胞瘤的血管形成病变。术前栓塞,然后通过腔内刮除进行切除,导致症状缓解至干预后 9 个月。尽管作者建议,但当时患者怀孕,并要求不再进行其他后续影像学检查。作者提出了首例报告的骶骨梭形细胞血管内皮细胞瘤病例,并复习了目前的文献。