Lang F F, Macdonald O K, Fuller G N, DeMonte F
Department of Neurosurgery, M. D. Anderson Cancer Center, The University of Texas, Houston 77030-4095, USA.
J Neurosurg. 2000 Dec;93(6):940-50. doi: 10.3171/jns.2000.93.6.0940.
Primary meningiomas arising outside the intracranial compartment (primary extradural meningiomas [PEMs]) are rare tumors. To develop a better understanding of these tumors and to establish a comprehensive classification scheme for them, the authors analyzed a series of patients treated at the M. D. Anderson Cancer Center (MDACC) and reviewed all cases reported in the English-language literature since the inception of the use of computerized tomography (CT) scanning.
Clinical records, results of radiographic studies, and histological slides were reviewed for all cases of PEM at MDACC. Demographic features, symptoms, tumor location, histological grade, and patient outcome were assessed in all cases. A comprehensive literature search identified 168 PEMs in 142 patients reported during the CT era. These reports were also analyzed for common features. Tumors for both data sets were classified as purely extracalvarial (Type I), purely calvarial (Type II), and calvarial with extracalvarial extension (Type III). Type II and Type III tumors were further categorized as convexity (C) or skull base (B) lesions. The incidence of PEMs at MDACC was 1.6%, which was consistent with the rate reported in the literature. In both data sets, the male/female ratio was nearly 1:1. The most common presenting symptom was a gradually expanding mass. The age of patients at diagnosis of PEM was bimodal, peaking during the second decade and during the fifth to seventh decades. In all MDACC cases and in 90% of those reported in the literature the PEMs were located in the head and neck. The majority of tumors originated in the skull (70%). In the MDACC series and in the literature review, the majority (67% and 89%, respectively) of tumors were histologically benign. Although fewer PEMs were malignant or atypical (33% at MDACC and 11% in the literature), their incidence was higher than that observed for primary intracranial meningiomas. Distant metastasis was not a common feature reported for patients with PEMs (6% in the literature). Outcome data were available in 96 of the cases culled from the CT-era literature. The combination of the MDACC data and the data obtained from the literature demonstrated that patients with benign Type IIB or Type IIIB lesions were more likely to experience recurrence than patients with benign Type IIC or Type IIIC tumors (26% compared with 0%, p < 0.05). The more aggressive atypical and malignant tumors were associated with a statistically significant higher death rate (29%) relative to benign tumors (4.8% death rate, p < 0.004).
Defining a tumor as a PEM is dependent on the tumor's relation to the dura mater and the extent and direction of its growth. Classification of PEMs as calvarial or extracalvarial and as convexity or skull base lesions correlates well with clinical outcome.
起源于颅内腔隙之外的原发性脑膜瘤(原发性硬膜外脑膜瘤[PEMs])是罕见肿瘤。为了更好地了解这些肿瘤并为其建立一个全面的分类方案,作者分析了在MD安德森癌症中心(MDACC)接受治疗的一系列患者,并回顾了自计算机断层扫描(CT)开始应用以来英文文献中报道的所有病例。
对MDACC所有PEM病例的临床记录、影像学研究结果和组织学切片进行回顾。评估所有病例的人口统计学特征、症状、肿瘤位置、组织学分级和患者预后。全面的文献检索确定了CT时代报道的142例患者中的168例PEM。还对这些报告的共同特征进行了分析。两个数据集的肿瘤分为单纯颅外(I型)、单纯颅骨(II型)和颅骨伴颅外扩展(III型)。II型和III型肿瘤进一步分为凸面(C)或颅底(B)病变。MDACC的PEM发病率为1.6%,与文献报道的发病率一致。在两个数据集中,男女比例接近1:1。最常见的首发症状是逐渐增大的肿块。PEM诊断时患者年龄呈双峰分布,在第二个十年以及第五至第七个十年达到峰值。在MDACC的所有病例以及文献报道的90%的病例中,PEM位于头颈部。大多数肿瘤起源于颅骨(70%)。在MDACC系列和文献综述中,大多数肿瘤(分别为67%和89%)在组织学上是良性的。虽然恶性或非典型PEM较少(MDACC为33%,文献中为11%),但其发病率高于原发性颅内脑膜瘤。远处转移不是PEM患者常见的特征(文献中为6%)。从CT时代文献中筛选出的96例病例有预后数据。MDACC数据与文献数据相结合表明,与良性IIC型或IIIC型肿瘤患者相比,良性IIB型或IIIB型病变患者更易复发(分别为26%和0%,p<0.05)。与良性肿瘤(死亡率4.8%)相比,侵袭性更强的非典型和恶性肿瘤的死亡率在统计学上显著更高(29%,p<0.004)。
将肿瘤定义为PEM取决于肿瘤与硬脑膜的关系及其生长范围和方向。将PEM分类为颅骨或颅外以及凸面或颅底病变与临床预后密切相关。