Yang Yang, Fang Jingyi, Li D A, Wang Liang, Ji Nan, Zhang Junting
Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, P.R. China.
Department of Neuropathology, Beijing Neurosurgical Institute, Capital Medical University, Beijing 100050, P.R. China.
Oncol Lett. 2016 May;11(5):3395-3402. doi: 10.3892/ol.2016.4386. Epub 2016 Mar 29.
Neurenteric cysts (NCs) are uncommon congenital cystic lesions. Malignantly transformed NCs are extremely rare. The present study reports the case of a recurrent foramen magnum NC with a malignant transformation and reviews 8 previously reported cases. A 58-year-old woman with a 5-month history of occasional headaches, dizziness and vomiting presented to the Beijing Tiantan Hospital (Beijing, China) with palsy of the left cranial IX and X nerves, decreased sensation in the limbs on the right side and an ataxic gait. Magnetic resonance imaging (MRI) scans revealed a cystic mass in the left side of the foramen magnum, positioned anteriolaterally to the medulla oblongata. Surgery using a left suboccipital retrosigmoid approach was performed. The lesion was partially resected and was histopathologically diagnosed as an NC with focal hyperplasia of the epithelial cells. Additional MRI scans that were performed 25 months later revealed a solid lesion posterior to the medullar oblongata. Therefore, surgery using a suboccipital midline approach was performed. The solid lesion was sub-totally removed and was histopathologically diagnosed as a well-differentiated papillary adenocarcinoma. At 1 month post-surgery, the patient's condition worsened, eventually resulting in mortality due to respiratory failure. Based on the findings of the present case and previous literature, strict criteria for malignant-transformed NCs were created. The location distribution of malignant-transformed NCs does not coincide with the location distribution of all NCs, and malignantly transformed NCs usually occur in adult patients and present as atypical radiological features. Surgery is the optimal treatment for malignantly transformed NCs, and the effectiveness of adjuvant therapy requires additional studies.
神经肠囊肿(NCs)是罕见的先天性囊性病变。恶性转化的神经肠囊肿极为罕见。本研究报告了一例复发性枕骨大孔神经肠囊肿发生恶性转化的病例,并回顾了8例先前报道的病例。一名58岁女性,有5个月偶尔头痛、头晕和呕吐的病史,因左侧Ⅸ、Ⅹ颅神经麻痹、右侧肢体感觉减退和共济失调步态就诊于北京天坛医院(中国北京)。磁共振成像(MRI)扫描显示枕骨大孔左侧有一个囊性肿块,位于延髓前外侧。采用左枕下乙状窦后入路进行手术。病变部分切除,组织病理学诊断为神经肠囊肿伴上皮细胞局灶性增生。25个月后进行的额外MRI扫描显示延髓后方有一个实性病变。因此,采用枕下中线入路进行手术。实性病变次全切除,组织病理学诊断为高分化乳头状腺癌。术后1个月,患者病情恶化,最终因呼吸衰竭死亡。基于本病例的发现和既往文献,制定了恶性转化神经肠囊肿的严格标准。恶性转化神经肠囊肿的部位分布与所有神经肠囊肿的部位分布不一致,恶性转化神经肠囊肿通常发生在成年患者中,并表现出非典型的影像学特征。手术是恶性转化神经肠囊肿的最佳治疗方法,辅助治疗的有效性需要进一步研究。