Bergin D J, Johnson T E, Spencer W H, McCord C D
Department of Surgery, Letterman Army Medical Center, Presidio of San Francisco.
Am J Ophthalmol. 1988 Feb 15;105(2):146-9. doi: 10.1016/0002-9394(88)90177-8.
We examined a 15-year-old boy who had a ganglioglioma involving the left optic nerve, which caused proptosis, decreased vision, and optic atrophy. Computed tomography demonstrated an intraconal mass along the course of the orbital portion of the optic nerve. The only evidence of systemic neurofibromatosis was axillary freckling. The patient underwent a combined medial and lateral orbitotomy and excision of the tumor. Histologic examination demonstrated a mass composed of neurons and glial cells characteristic of ganglioglioma. After a one-year follow-up period, we have found no evidence of recurrence.
我们检查了一名15岁男孩，他患有累及左侧视神经的神经节胶质瘤，导致眼球突出、视力下降和视神经萎缩。计算机断层扫描显示沿视神经眶部走行的肌锥内肿块。系统性神经纤维瘤病的唯一证据是腋窝雀斑。患者接受了内侧和外侧眶切开术联合肿瘤切除术。组织学检查显示肿块由神经节胶质瘤特有的神经元和神经胶质细胞组成。经过一年的随访，我们未发现复发迹象。
