Lucas C, Benderitter T, Choux M
Arch Fr Pediatr. 1982 May;39(5):303-7.
17 children presenting with craniopharyngioma were studied from 1970 to 1980. Presenting symptoms were usually reflecting endocrine dysfunction (13 of 17 cases), such as growth retardation, weight abnormalities, diabetes insipidus and hypothyroidism. Unfortunately, these signs were most often misinterpreted (10 of 13 cases) so that when diagnosis was made dissociated hypopituitarism was present. Further impairment of endocrine function always followed surgical excision. In most children pituitary insufficiency becomes complete and permanent. These results are similar whatever the tumor site and surgical procedure. Growth goes on and puberty occurs without treatment in a few cases but in the majority of them substitutive therapy is necessary.
1970年至1980年期间对17例颅咽管瘤患儿进行了研究。首发症状通常反映内分泌功能障碍(17例中有13例),如生长发育迟缓、体重异常、尿崩症和甲状腺功能减退。不幸的是,这些症状最常被误诊(13例中有10例),以至于确诊时已出现分离性垂体功能减退。内分泌功能的进一步损害总是在手术切除后出现。在大多数儿童中,垂体功能不全变得完全且永久。无论肿瘤部位和手术方式如何,结果都是相似的。少数病例未经治疗仍能继续生长并进入青春期,但大多数病例需要替代治疗。