Schneider Arthur B, Ron Elaine, Lubin Jay, Stovall Marilyn, Shore-Freedman Eileen, Tolentino Jocelyn, Collins Barbara J
University of Illinois College of Medicine, Section of Endocrinology, Diabetes and Metabolism, Chicago, IL 60612, USA.
Neuro Oncol. 2008 Feb;10(1):73-8. doi: 10.1215/15228517-2007-047. Epub 2007 Dec 13.
Childhood radiation exposure has been associated with an increased risk for developing several neoplasms, particularly benign and malignant thyroid tumors, but little is known about the risk of developing acoustic neuromas. The aim of this study was to confirm whether there is a risk for acoustic neuromas and, if so, to determine its magnitude and duration. We investigated the time trend and dose-response relationships for acoustic neuroma incidence in a cohort of 3,112 individuals who were irradiated as children between 1939 and 1962. Most of the patients were treated to reduce the size of their tonsils and adenoids and received substantial radiation exposure to the cerebellopontine angle, the site of acoustic neuromas. Forty-three patients developed benign acoustic neuromas, forty of them surgically resected, far in excess of what might be expected from data derived from brain tumor registries. The mean dose (+/-SD) to the cerebellopontine angle was 4.6 +/- 1.9 Gy. The relative risk per Gy was 1.14 (95% confidence interval 1.0-1.3). The earliest case occurred 20.4 years after exposure and the latest 55 years after exposure (mean 38.3 +/- 10.1 years). Our study provides support for an association between acoustic neuromas and childhood radiation exposure. Although acoustic neuromas are usually benign and often asymptomatic, many cause significant morbidity. Following childhood radiation exposure, they appear after a long latency and continue to occur many decades afterward. Any symptoms of an acoustic neuroma in a patient with a history of radiation to the head and neck area should be investigated carefully, and the threshold for employing imaging should be lowered.
儿童期接受辐射与患多种肿瘤的风险增加有关,尤其是良性和恶性甲状腺肿瘤,但对于患听神经瘤的风险却知之甚少。本研究的目的是确认是否存在患听神经瘤的风险,如果存在,则确定其风险程度和持续时间。我们调查了1939年至1962年间儿童期接受过辐射的3112名个体队列中听神经瘤发病率的时间趋势和剂量反应关系。大多数患者接受治疗以缩小扁桃体和腺样体的大小,并接受了大量辐射至桥小脑角,即听神经瘤的发病部位。43名患者患上了良性听神经瘤,其中40例接受了手术切除,远远超过了根据脑肿瘤登记数据预期的数量。桥小脑角的平均剂量(±标准差)为4.6±1.9 Gy。每Gy的相对风险为1.14(95%置信区间1.0 - 1.3)。最早的病例在接触辐射后20.4年出现,最晚的在接触辐射后55年出现(平均38.3±10.1年)。我们的研究为听神经瘤与儿童期辐射暴露之间的关联提供了支持。尽管听神经瘤通常是良性的且常常无症状,但许多会导致严重的发病情况。儿童期接受辐射后,它们在很长的潜伏期后出现,并在几十年后仍持续发生。对于有头颈部辐射史的患者,任何听神经瘤的症状都应仔细调查,并且应降低采用影像学检查的阈值。