Sznajder L, Abrahams C, Parry D M, Gierlowski T C, Shore-Freedman E, Schneider A B
Department of Medicine, University of Illinois at Chicago, USA.
Arch Intern Med. 1996 Sep 9;156(16):1873-8.
To determine the pattern of neural tumors (schwannomas, vestibular schwannomas [acoustic neuromas], and meningiomas) that developed in 3013 people who received radiation treatment with x-ray beam therapy for benign conditions of the head and neck area before their 16th birthday.
The surgical and pathology reports and pathology slides were reviewed for all neural tumors in the cohort. Patients with more than 1 neural tumor were compared with those with 1 neural tumor and those with no neural tumors.
There were 7 patients with multiple neural tumors and 63 with single neural tumors. The distribution of tumors in these 2 groups differed. The group with multiple tumors had more spinal nerve root schwannomas, while the group with single tumors had more cranial nerve schwannomas. Six of the 7 patients did not meet the diagnostic criteria for neurofibromatosis type 2.
Our findings suggest that host factors that increase susceptibility to radiation may be involved in the development of the multiple neural tumors. Clinically, patients with multiple neural tumors who do not meet the diagnostic criteria for neurofibromatosis type 2 should be questioned about radiation exposure. If exposure is confirmed, then screening for other radiation-related tumors should be initiated.
确定16岁之前因头颈部良性疾病接受X射线束放射治疗的3013人中发生的神经肿瘤(神经鞘瘤、前庭神经鞘瘤[听神经瘤]和脑膜瘤)的发病模式。
对队列中所有神经肿瘤的手术和病理报告以及病理切片进行审查。将患有1个以上神经肿瘤的患者与患有1个神经肿瘤的患者以及未患神经肿瘤的患者进行比较。
有7例患者患有多发性神经肿瘤,63例患有单发性神经肿瘤。这两组肿瘤的分布有所不同。多发性肿瘤组的脊神经根神经鞘瘤更多,而单发性肿瘤组的脑神经神经鞘瘤更多。7例患者中有6例不符合2型神经纤维瘤病的诊断标准。
我们的研究结果表明,增加辐射易感性的宿主因素可能与多发性神经肿瘤的发生有关。临床上,对于不符合2型神经纤维瘤病诊断标准的多发性神经肿瘤患者,应询问其辐射暴露情况。如果确认有暴露史,则应开始筛查其他与辐射相关的肿瘤。