Asari J, Yamanobe K, Sasaki T, Yamao N, Kodama N
Department of Neurosurgery, Fukushima Medical School, Japan.
No Shinkei Geka. 1987 Dec;15(12):1313-8.
A surgical case of prolactinoma associated with craniopharyngioma is reported. A 47-year-old man was admitted to some neurosurgical clinic on October 12, 1982, because of visual disturbance, general fatigue and impotence. Laboratory study revealed hyperprolactinemia (360 ng/ml) and slight enlargement of sella turcica indicated the pituitary adenoma. Transsphenoidal surgery was performed to remove the tumor on November 20, 1982. Histopathological examination revealed chromophobe adenoma, and prolactin was stained in the tumor cells by means of immunoperoxidase staining. Though the clinical symptoms had been improved after surgery, visual disturbance became worse about one month later. At that time empty sella syndrome was suspected and the second operation (interhemispheric approach) was performed on January 21, 1983. No pathological changes were observed at all. On July 13, 1983, he was transferred to our clinic, because his visual acuity was deteriorating. At this time we reviewed the previous CT scan and noticed a suprasellar mass. It was supposed that the lesion had been overlooked and was the cause of the visual disturbance. On August 1, 1983, a bifrontal craniotomy was performed and the suprasellar tumor was removed. Pathological examination of the tumor revealed craniopharyngioma. So it was supposed that pituitary adenoma and craniopharyngioma had been coexisting since onset. Except for cases with von Recklinghausen's disease, multiple primary intracranial tumors of different cell types are relatively rare. A review of literature revealed 94 cases until 1986. The most frequent combination of multiple tumors was meningioma and glioma. But we could not find any case of pituitary adenoma associated with craniopharyngioma in the literature.(ABSTRACT TRUNCATED AT 250 WORDS)
本文报告了一例与颅咽管瘤相关的泌乳素瘤手术病例。1982年10月12日,一名47岁男性因视力障碍、全身乏力和阳痿入住某神经外科诊所。实验室检查发现高泌乳素血症(360 ng/ml),蝶鞍轻度增大提示垂体腺瘤。1982年11月20日进行经蝶窦手术切除肿瘤。组织病理学检查显示为嫌色性腺瘤,通过免疫过氧化物酶染色在肿瘤细胞中检测到泌乳素。虽然术后临床症状有所改善,但约一个月后视力障碍加重。当时怀疑有空蝶鞍综合征,并于1983年1月21日进行了第二次手术(经半球间入路),未观察到任何病理变化。1983年7月13日,因其视力恶化转至我院。此时我们复查了之前的CT扫描,发现鞍上有一肿块。推测该病变之前被漏诊,是视力障碍的原因。1983年8月1日,进行双额开颅手术,切除鞍上肿瘤。肿瘤病理检查显示为颅咽管瘤。因此推测垂体腺瘤和颅咽管瘤自发病起就并存。除了冯·雷克林豪森病患者外,不同细胞类型的多发性原发性颅内肿瘤相对少见。文献回顾显示,截至1986年共有94例。最常见的多发性肿瘤组合是脑膜瘤和胶质瘤。但我们在文献中未找到任何垂体腺瘤与颅咽管瘤相关的病例。(摘要截短至250字)