Carrasco Moro Rodrigo, Jiménez Zapata Herbert D, Pian Arias Héctor, Martínez San Millán Juan S, Martínez Rodrigo María A, Pascual Garvi José M
Servicio de Neurocirugía, H. U. Ramón y Cajal, Madrid, España.
Servicio de Neurocirugía, H. U. Ramón y Cajal, Madrid, España.
Neurocirugia (Engl Ed). 2019 Jan-Feb;30(1):1-10. doi: 10.1016/j.neucir.2018.08.002. Epub 2018 Sep 25.
Meningiomas associating prominent cystic changes (CM) have challenged neurosurgeons since the beginning of this surgical discipline. We present the experience in the diagnostic and therapeutic management of this entity in our institution.
A review of our patient database was carried out, searching for those CM that were operated on in the last 15 years. Relevant clinical data were recorded and analyzed for each case, with special emphasis in the correlation of radiological and pathological findings. Cystic changes were classified according to the scheme proposed by Nauta et al. RESULTS: A total of 11 patients were gathered, which represents 1.8% of the meningiomas operated on in our department during the period studied. All were adults, predominantly female patients (8 cases). Among the clinical symptoms a high rate of epileptic seizures was observed while only one patient developed acute intracranial hypertension. Morphologically, most tumors corresponded to type 2 CMs, followed by types 1, 3 and 4. In only five patients an unequivocal radiological diagnosis of meningioma could be made. All neoplasms were surgically removed and there were no records of recurrence (mean follow-up: 52.8 months). Microscopic findings were consistent with the pathological diagnosis of atypical meningioma in 4 cases, while the remaining tumors corresponded to OMS grade I neoplasms with variable microscopic patterns.
Meningiomas can exceptionally associate cystic changes, both intra and/or extratumoral, in variable number and size. When cystic changes become too prominent (a large number or big-sized cysts), a serious preoperative diagnostic dilemma may arise. The surgical management of those CMs displaying a peripheral, thin-walled cyst (types 2 and 3) is especially complex, as contrast enhancement of the tumor wall did not correlate strictly with neoplastic invasion; even in the absence of this feature free floating islands of meningothelial cells intermixed with cyst fluid can be found. Consequently both surgical biopsy of every suspicious tissue and copious irrigation of the surgical cavity are strongly recommended for these CM types.
自神经外科这一手术学科创立之初,伴有显著囊性改变(CM)的脑膜瘤就一直困扰着神经外科医生。我们在此介绍本机构对该实体疾病的诊断和治疗经验。
对我们的患者数据库进行了回顾,筛选出过去15年内接受手术治疗的CM患者。记录并分析了每个病例的相关临床数据,特别强调了放射学和病理学结果的相关性。根据Nauta等人提出的方案对囊性改变进行分类。结果:共收集到11例患者,占我们科室在研究期间所手术治疗的脑膜瘤患者的1.8%。所有患者均为成年人,以女性患者为主(8例)。在临床症状中,癫痫发作的发生率较高,而只有1例患者出现急性颅内高压。形态学上,大多数肿瘤符合2型CM,其次是1型、3型和4型。只有5例患者能够通过放射学明确诊断为脑膜瘤。所有肿瘤均通过手术切除,且无复发记录(平均随访时间:52.8个月)。显微镜检查结果显示,4例符合非典型脑膜瘤的病理诊断,其余肿瘤为I级脑膜瘤,具有不同的显微镜下表现。
脑膜瘤可罕见地伴有瘤内和/或瘤外的囊性改变,其数量和大小各不相同。当囊性改变过于显著(大量或大尺寸囊肿)时,术前可能会出现严重的诊断困境。对于那些表现为周边薄壁囊肿(2型和3型)的CM,手术治疗尤其复杂,因为肿瘤壁的强化与肿瘤侵袭并不严格相关;即使没有这种特征,也可在囊液中发现游离的脑膜上皮细胞岛。因此,对于这些CM类型,强烈建议对每个可疑组织进行手术活检,并对手术腔进行大量冲洗。