Miyagi Atsushi, Katayama Yoichi
Department of Neurosurgery, Shirahigebashi Hospital, Tokyo, Japan.
Neurosurgery. 2007 Jan;60(1):E203-4; discussion E204. doi: 10.1227/01.NEU.0000249255.71170.C0.
Supratentorial neurenteric cysts (NC) are rare; only 16 cases were reported previously, the majority of which were located in the anterior fossa or in the deep midline structure. We report a case of NC arising in the high convexity parietal lesion and briefly discuss the histogenesis of NC in such an unusual location.
A 63-year-old man presented with a 1-month history of progressive headache and dizziness. Computed tomographic and magnetic resonance imaging scans demonstrated a 4 x 5 x 5 cm extra-axial cystic lesion in the right parietal convexity adjacent to the sagittal sinus without contrast enhancement. A translucent thin-walled cyst containing a milky-white fluid was partially excised via a right parietal craniotomy.
The cyst wall was composed of a thin fibroconnective tissue lined by a single layer of ciliated columnar epithelial cells and pseudostratified columnar epithelium. Mucous-secreting goblet cells of epithelial lining reacted to periodic acid-Shiff staining. The internal epithelial cells were immunoreactive to cytokeratin and epithelial membrane antigen, but not to carcinoembryonic antigen, glial fibrillary acidic protein, or S-100 protein. A follow-up magnetic resonance imaging scan taken 6 months later showed resolution of mass effect without evidence of cyst recurrence. The patient was discharged home in excellent condition.
A case of NC arising in the high convexity parietal lesion is described. Supratentorial NCs located far from the location of the primitive endoderm suggest the possibility that NCs could arise from ectopic endodermal tissue through an undetermined process of anomalous differentiation. Total surgical excision of the cyst wall and contents is the best treatment for the symptomatic cases. Subtotal or partial resection without injury to important neurovascular structures are reasonable alternatives, but long-term careful follow-up magnetic resonance imaging or computed tomography is necessary to monitor for recurrence of any residual lesion.
幕上神经肠囊肿(NC)较为罕见;此前仅报道过16例,其中大多数位于前颅窝或深部中线结构。我们报告1例发生于高凸部顶叶病变的NC病例,并简要讨论NC在如此不寻常位置的组织发生。
一名63岁男性,有1个月进行性头痛和头晕病史。计算机断层扫描和磁共振成像扫描显示,在右侧顶叶凸部矢状窦旁有一个4×5×5 cm的轴外囊性病变,无强化。通过右顶叶开颅手术部分切除了一个含有乳白色液体的半透明薄壁囊肿。
囊肿壁由一层薄的纤维结缔组织构成,内衬单层纤毛柱状上皮细胞和假复层柱状上皮。上皮内衬的黏液分泌杯状细胞对过碘酸-希夫染色有反应。内部上皮细胞对细胞角蛋白和上皮膜抗原呈免疫反应,但对癌胚抗原、胶质纤维酸性蛋白或S-100蛋白无反应。6个月后进行的随访磁共振成像扫描显示占位效应消失,无囊肿复发迹象。患者出院时情况良好。
描述了1例发生于高凸部顶叶病变的NC病例。位于远离原始内胚层位置的幕上NC提示,NC可能通过未确定的异常分化过程起源于异位内胚层组织。对于有症状的病例,完整切除囊肿壁和内容物是最佳治疗方法。在不损伤重要神经血管结构的情况下进行次全或部分切除是合理的替代方案,但需要长期仔细的随访磁共振成像或计算机断层扫描以监测任何残留病变的复发情况。