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颅内孤立性纤维瘤伴延迟性症状性腰椎转移:病例说明

Intracranial solitary fibrous tumor with delayed symptomatic metastasis to the lumbar spine: illustrative case.

作者信息

Menaker Simon A, Ljubimov Vladimir A, Krutikova Viktoria O, Urnes Cole, Bannykh Serguei I, Ross Lindsey B, Eboli Paula

机构信息

Departments of1Neurosurgery, and.

3Touro University College of Osteopathic Medicine, Henderson, Nevada; and.

出版信息

J Neurosurg Case Lessons. 2023 Feb 13;5(7). doi: 10.3171/CASE22495.

Abstract

BACKGROUND

Intracranial solitary fibrous tumors (SFTs), formerly known as hemangiopericytomas, are rare, aggressive mesenchymal extra-axial tumors typically treated via resection, often with preoperative embolization and postoperative radiation and/or antiangiogenic therapy. Although surgery confers a significant survival benefit, local recurrence and distant metastasis are not uncommon and may occur in a delayed fashion.

OBSERVATIONS

The authors describe the case of a 29-year-old male who initially presented with headache, visual disturbance, and ataxia, and was found to have a large right tentorial lesion with mass effect on surrounding structures. He underwent tumor embolization and resection with gross total resection achieved and pathology consistent with World Health Organization grade 2 hemangiopericytoma. The patient recovered well, but 6 years later presented with low back pain and lower extremity radiculopathy and was found to have metastatic disease within the L4 vertebral body causing moderate central canal stenosis. This was successfully treated with tumor embolization followed by spinal decompression and posterolateral instrumented fusion. Metastasis of intracranial SFT to vertebral bone is exceedingly rare. To our knowledge this is only the 16th reported case.

LESSONS

Serial surveillance for metastatic disease is imperative in patients with intracranial SFTs given their propensity and unpredictable time course for distant spread.

摘要

背景

颅内孤立性纤维瘤(SFT),以前称为血管外皮细胞瘤,是一种罕见的、侵袭性的间叶性轴外肿瘤,通常通过手术治疗,术前常进行栓塞,术后进行放疗和/或抗血管生成治疗。虽然手术能带来显著的生存益处,但局部复发和远处转移并不少见,且可能延迟发生。

观察结果

作者描述了一例29岁男性患者,最初表现为头痛、视力障碍和共济失调,发现右侧小脑幕有一个大的病变,对周围结构有占位效应。他接受了肿瘤栓塞和切除术,实现了全切,病理结果符合世界卫生组织2级血管外皮细胞瘤。患者恢复良好,但6年后出现腰痛和下肢神经根病,发现L4椎体有转移性疾病,导致中度中央管狭窄。通过肿瘤栓塞,随后进行脊柱减压和后外侧器械融合,成功治疗了该疾病。颅内SFT转移至椎骨极为罕见。据我们所知,这是第16例报道的病例。

经验教训

鉴于颅内SFT患者有远处转移的倾向且转移时间不可预测,对其进行转移性疾病的连续监测至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b40/10550599/e9a57df9c7d5/CASE22495f1.jpg

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