Linggood R M, Hsu D W, Efird J T, Pardo F S
Laboratory of Molecular/Tumor Radiation Biology, Massachusetts General Hospital, Boston 02114, USA.
J Neurooncol. 1995 Oct;26(1):45-51. doi: 10.1007/BF01054768.
Little is known of the molecular genetic mechanisms contributing to meningioma tumor progression. We evaluated a total of 26 clinical cases of meningioma: twenty three patients with meningioma treated at our institution between 1978 and 1990 and three asymptomatic cases found initially at autopsy. In addition, histologically normal meninges obtained at post-mortem examination from 5 cases were evaluated. There were 13 men and 10 women in the patient group with a median age of 48.7 years, treated by surgery and/or irradiation. Median follow-up was 46 months (range 16-152 months). Archival cases and age-matched normal meningeal tissue obtained at autopsy during the same time period were obtained for study. Patients with TGF alpha scores greater than 3.0 were more likely to fail treatment and had lower overall survival times than those with immunostaining scores of 1 or 2. Three autopsy cases where meningioma had been silent clinically had overall staining scores of 0.75, while 10 samples of normal meninges harvested from 5 cases at autopsy had staining scores of 0. Two patients each underwent 3 surgeries for recurrent tumor, serial specimens showed increased TGF alpha expression over time, though all material from these procedures was consistent with the diagnosis of histologically benign meningioma.
关于脑膜瘤肿瘤进展的分子遗传机制,人们了解甚少。我们共评估了26例脑膜瘤临床病例:23例于1978年至1990年间在我们机构接受治疗的脑膜瘤患者,以及3例最初在尸检时发现的无症状病例。此外,还评估了5例死后检查获得的组织学正常的脑膜。患者组中有13名男性和10名女性,中位年龄为48.7岁,接受了手术和/或放疗。中位随访时间为46个月(范围16 - 152个月)。获取了同期存档病例以及尸检时获得的年龄匹配的正常脑膜组织用于研究。转化生长因子α(TGFα)评分大于3.0的患者比免疫染色评分为1或2的患者更易治疗失败且总生存时间更短。3例临床上无症状的脑膜瘤尸检病例的总体染色评分为0.75,而从5例尸检病例中获取的10份正常脑膜样本的染色评分为0。两名患者因复发性肿瘤各自接受了3次手术,系列标本显示随着时间推移TGFα表达增加,尽管这些手术的所有材料在组织学上均符合良性脑膜瘤的诊断。