Jankovic Dragan, Vuong Kyna, Splavski Bruno, Rotim Kresimir, Arnautovic Kenan I
Department of Neurosurgery, University Medical Centre of the Johannes Gutenberg University of Mainz, Mainz, Germany; Faculty of Medicine, Josip Juraj Strossmayer University, Osijek, Croatia.
Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
World Neurosurg. 2023 May;173:48-62. doi: 10.1016/j.wneu.2023.02.071. Epub 2023 Feb 22.
Supratentorial hemangioblastomas are benign and highly vascularized neoplasms that appear most often in the spine and posterior cranial fossa. They can also be located in the supratentorial compartment of the brain. We conducted a systematic review of the literature to better understand the clinical insights of supratentorial hemangioblastoma in adults.
Using Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, the authors reviewed the English-language literature in the PubMed/MEDLINE database on supratentorial hemangioblastoma in adults, published in the past 40 years. We analyzed the differences between sporadic hemangioblastomas and hemangioblastomas associated with von Hippel-Lindau disease. In addition, we compared the characteristics of supratentorial hemangioblastomas with infratentorial and spinal cord locations.
We reviewed 92 articles, describing 157 supratentorial hemangioblastomas in a total cohort of 148 adult patients. Most articles reporting supratentorial hemangioblastomas were published in the United States. Supratentorial hemangioblastomas occur more frequently in women than men. The median age at the time of diagnosis was 44.48 years. The sellar/parasellar region was the most commonly tumor location, while the most common morphological type was the solid type. Almost 80% of hemangioblastomas were completely resected; the outcome was favorable in more than 3 fourth of patients.
Given their rarity, the literature on supratentorial hemangioblastomas is limited and based mostly on case reports. Complete surgical resection is the first choice of treatment and is associated with a good treatment outcome.
幕上血管母细胞瘤是良性且血管高度丰富的肿瘤,最常出现在脊柱和后颅窝。它们也可位于脑的幕上间隙。我们对文献进行了系统回顾,以更好地了解成人幕上血管母细胞瘤的临床见解。
作者按照系统评价和荟萃分析的首选报告项目指南,检索了过去40年在PubMed/MEDLINE数据库中发表的关于成人幕上血管母细胞瘤的英文文献。我们分析了散发性血管母细胞瘤与冯·希佩尔-林道病相关血管母细胞瘤之间的差异。此外,我们比较了幕上血管母细胞瘤与幕下及脊髓部位血管母细胞瘤的特征。
我们回顾了92篇文章,共描述了148例成年患者中的157例幕上血管母细胞瘤。大多数报道幕上血管母细胞瘤的文章发表于美国。幕上血管母细胞瘤在女性中比男性更常见。诊断时的中位年龄为44.48岁。鞍区/鞍旁区域是最常见的肿瘤部位,而最常见的形态学类型是实体型。几乎80%的血管母细胞瘤被完全切除;超过四分之三的患者预后良好。
鉴于其罕见性,关于幕上血管母细胞瘤的文献有限,且大多基于病例报告。完整的手术切除是首选治疗方法,且与良好的治疗结果相关。