Ahmed Nazmin, Ferini Gianluca, Barua Kanak Kanti, Halder Rathin, Barua Sudip, Priola Stefano, Tomasi Ottavio, Umana Giuseppe Emmanuele, Shlobin Nathan A, Scalia Gianluca, Garg Kanwaljeet, Chaurasia Bipin
Department of Neurosurgery, Ibrahim Cardiac Hospital and Research Institute, Shahbagh, Dhaka 1000, Bangladesh.
Department of Radiation Oncology, REM Radioterapia srl, 95029 Viagrande, Italy.
Life (Basel). 2022 Jun 21;12(7):931. doi: 10.3390/life12070931.
(1) Introduction: Adult-onset pilocytic astrocytoma (APA) accounts for only 1.5% of all brain tumors, and studies regarding APA are limited. This review is focused on the history, clinical course, cytogenetics, neuroimaging features, management, and outcome of APAs. (2) Methods: Using a systematic search protocol in Google Scholar, PubMed, and Science Direct databases, the authors extracted cases of APA predilecting the temporal lobe from inception to December 2020. Articles lacking necessary data were excluded from this study. Data were analyzed using IBM SPSS 23 statistical package software. (3) Results: A total of 32 patients, 14 (43.8%) males and 18 (56.2%) females, with a male/female ratio of 0.77/1, were grouped. The mean age of the patients was 34.22 ± 15.17 years, ranging from 19 to 75. The tumors were predominantly located in the left side. We have also discussed the clinical presentation, and headache was the most common complaint, followed by visual disturbance. Preoperative neuroimaging features demonstrated cystic lesions in 16 patients, with mural nodule in 5 patients; intracerebral hemorrhage was present in 1 patient, and solid enhancing mass was observed in 3 patients. Only our reported case presented as a solid calcified mass. Most of the patients (78.1%) underwent a gross total resection (GTR), only 5 (21.9%) underwent subtotal resection (STR). The outcome and prognosis history were excellent, and no recurrence was observed. (4) Conclusion: Most of the APAs of the temporal lobe follow benign clinical courses, but some patients exhibit aggressive clinical behavior. There was no history of recurrence after treatment at up to 27 years of follow-up.
(1) 引言:成人型毛细胞型星形细胞瘤(APA)仅占所有脑肿瘤的1.5%,关于APA的研究有限。本综述聚焦于APA的病史、临床病程、细胞遗传学、神经影像学特征、治疗及预后。(2) 方法:作者采用系统检索方案,在谷歌学术、PubMed和科学Direct数据库中,提取自起始至2020年12月间累及颞叶的APA病例。缺乏必要数据的文章被排除在本研究之外。使用IBM SPSS 23统计软件包对数据进行分析。(3) 结果:共纳入32例患者,其中男性14例(43.8%),女性18例(56.2%),男女比例为0.77/1。患者的平均年龄为34.22±15.17岁,年龄范围为19至75岁。肿瘤主要位于左侧。我们还讨论了临床表现,头痛是最常见的主诉,其次是视觉障碍。术前神经影像学特征显示,16例患者有囊性病变,5例有壁结节;1例有脑内出血,3例观察到实性强化肿块。仅我们报道的病例表现为实性钙化肿块。大多数患者(78.1%)接受了全切除(GTR),仅5例(21.9%)接受了次全切除(STR)。预后和转归情况良好,未观察到复发。(4) 结论:大多数颞叶APA遵循良性临床病程,但部分患者表现出侵袭性临床行为。随访长达27年,治疗后无复发史。