Department of Neurosurgery, Cannizzaro Hospital, Catania, Italy.
Department of Neurosurgery, Policlinico Universitario Agostino Gemelli, Roma, Lazio, Italy.
J Neurol Surg A Cent Eur Neurosurg. 2022 Mar;83(2):161-172. doi: 10.1055/s-0041-1739217. Epub 2021 Dec 20.
Spinal angiolipomas (SAs) are rare, benign tumors, representing 0.0004 to 1.2% of angiolipomas, usually located at the extradural and posterior thoracic level, with multimetameric extension.
A systematic literature review was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. The authors searched on PubMed and Scopus databases for published articles with the Mesh term "spinal angiolipoma" and pertinent associations. Language restriction to English papers was applied. The authors also reported three emblematic cases of patients who underwent surgical resection of spindle-shaped (type IA) and dumbbell-shaped (type II) SAs between 2014 and 2020.
Of the 256 retrieved articles, 33 were included in the meta-analysis. These 33 studies, together with our 3 reported cases, included a total of 60 patients, 36 females (60%) and 24 males (40%), with a mean age of 53.12 ± 12.82 years (range: 12-77 years).T5 was the most represented level (22 patients). Usually, the localization of SA was extradural, with 53 patients suffering from spindle-shaped type IA SA (88.3%) and 7 patients from dumbbell-shaped type II SA (11.6%). Almost all patients underwent laminectomy (78.3%) and presented a full recovery of motor deficits (85%). Gross total removal (GTR) was performed in 93.3% of patients. The mean follow-up was of 22.71 ± 21.45 months (range: 2-80 months). There was no documented recurrence at follow-up magnetic resonance imaging in any of the patients.
SAs are rare, benign tumors with a great vascular component that presents a favorable outcome. GTR is the gold standard treatment and usually an adjuvant therapy is not required. Even infiltrative lesions, which are more complex, can be treated successfully with a good prognosis. Dumbbell-shaped SAs must be differentiated from schwannomas and meningiomas, and require different surgical techniques, given the profuse bleeding associated with the attempt of debulking. En block resection is the key to treat these common benign tumors with acceptable blood loss.
脊髓血管脂肪瘤(SAs)是罕见的良性肿瘤,占血管脂肪瘤的 0.0004%至 1.2%,通常位于硬膜外和胸背部,呈多节段性延伸。
根据系统评价和荟萃分析的首选报告项目(PRISMA)声明,进行了系统的文献回顾。作者在 PubMed 和 Scopus 数据库中搜索了使用 Mesh 术语“脊髓血管脂肪瘤”和相关关联的已发表文章。应用了英语论文的语言限制。作者还报告了 3 例在 2014 年至 2020 年间接受纺锤形(IA 型)和哑铃形(II 型)SAs 手术切除的典型病例。
在检索到的 256 篇文章中,有 33 篇被纳入荟萃分析。这 33 项研究以及我们报告的 3 例病例共纳入 60 例患者,其中女性 36 例(60%),男性 24 例(40%),平均年龄为 53.12±12.82 岁(范围:12-77 岁)。T5 是最常见的受累水平(22 例)。通常,SA 的定位是硬膜外的,53 例患者患有纺锤形 IA 型 SA(88.3%),7 例患者患有哑铃形 II 型 SA(11.6%)。几乎所有患者均接受了椎板切除术(78.3%),并完全恢复了运动功能缺损(85%)。93.3%的患者行全切除(GTR)。患者的平均随访时间为 22.71±21.45 个月(范围:2-80 个月)。在任何患者的随访磁共振成像中均未记录到复发。
SAs 是罕见的良性肿瘤,具有很大的血管成分,预后良好。GTR 是金标准治疗,通常不需要辅助治疗。即使是侵袭性病变,由于与肿块切除相关的大量出血,手术也更加复杂,但仍可成功治疗,预后良好。哑铃形 SAs 必须与神经鞘瘤和脑膜瘤区分开来,并且由于与试图减瘤相关的大量出血,需要不同的手术技术。整块切除是治疗这些常见良性肿瘤的关键,出血量可接受。