Hoffman H J
Can J Neurol Sci. 1985 Nov;12(4):348-52. doi: 10.1017/s0317167100035514.
A review has been carried out of those patients with a craniopharyngioma who were treated initially in our institution and had a microsurgical excision of their tumour during the period of time when newer and sophisticated modalities of investigation and treatment were available. Twenty-nine patients with craniopharyngioma were treated initially by microsurgical excision of their tumour at the Hospital for Sick Children from January 1976 to June 1985. In 21 a total removal of the tumour was performed, and there has been no clinical evidence of recurrence. No deaths were recorded in any of the 29 patients. The principal morbidity has resulted from endocrine deficits that these patients exhibit.
对那些最初在我们机构接受治疗的颅咽管瘤患者进行了回顾性研究，这些患者在有更新、更先进的检查和治疗方式的时期接受了肿瘤的显微手术切除。1976年1月至1985年6月期间，29例颅咽管瘤患者最初在儿童医院接受了肿瘤显微手术切除。其中21例患者的肿瘤被完全切除，且无复发的临床证据。29例患者均无死亡记录。主要的发病率是由这些患者出现的内分泌缺陷导致的。
