Swinson Bradley M, Friedman William A, Yachnis Anthony T
Department of Neurosurgery, University of Florida, Gainesville 32610, USA.
Neurosurgery. 2006 May;58(5):E990; discussion E990. doi: 10.1227/01.NEU.0000210213.12847.1E.
Neurocytomas are typically located within the supratentorial ventricular system. Extraventricular neurocytomas are very rare, and this is only the second reported case of a pontine neurocytoma. We discuss the clinical presentation, histology, and treatment of these rare tumors.
A 58-year-old man presented with a 4-month history of headache and unilateral facial and distal extremity paresthesia. Magnetic resonance imaging (MRI) scans demonstrated a 2.6 x 2.2-cm ring-enhancing cystic mass in the right pons.
MRI-guided stereotactic biopsy yielded a diagnosis of atypical neurocytoma. Because of the location and malignant histological features of the tumor, the patient was initially treated with external beam radiation therapy. Several months later, MRI scans demonstrated tumor progression. The patient then underwent three rounds of temozolomide chemotherapy, during and after which his symptoms worsened. Aggressive subtotal resection of the tumor was achieved via a right suboccipital craniectomy.
Twenty-eight months postoperatively, the patient is symptom free, and MRI scans demonstrate no evidence of residual or recurrent tumor.
神经细胞瘤通常位于幕上脑室系统内。脑室外神经细胞瘤非常罕见,这是第二例报道的桥脑神经细胞瘤。我们讨论这些罕见肿瘤的临床表现、组织学及治疗方法。
一名58岁男性,有4个月的头痛及单侧面部和远端肢体感觉异常病史。磁共振成像(MRI)扫描显示右桥脑有一个2.6×2.2厘米的环形强化囊性肿块。
MRI引导下立体定向活检确诊为非典型神经细胞瘤。由于肿瘤的位置及恶性组织学特征,患者最初接受了外照射放疗。几个月后,MRI扫描显示肿瘤进展。患者随后接受了三轮替莫唑胺化疗,化疗期间及化疗后症状加重。通过右枕下开颅手术对肿瘤进行了积极的次全切除。
术后28个月,患者无症状,MRI扫描未显示残留或复发肿瘤的迹象。