Kurozumi Kazuhiko, Tabuchi Akira, Ono Yasuhiro, Tamiya Takashi, Ohmoto Takashi, Furuta Tomohisa, Hamasaki Shuji
Department of Neurological Surgery, Field of Neuroscience, Branch of Biophysical Science, Graduate School of Medicine and Dentistry, Okayama University, 2-5-1 Shikada-cho, Okayama-city, 700-8558, Japan.
No Shinkei Geka. 2002 Jul;30(7):741-5.
A case of pituitary adenoma associated is neurofibromatosis type 1 is reported. On June 6, 2000, a 49-year-old man was admitted to the Department of Neurological Surgery, Okayama University Hospital, for bitemporal hemianopsia. Twenty-nine years previously, he had been operated on for a left inguinal tumor that proved to be a neurofibroma. Based on the presence of other manifestations, such as café-au-lait spots and subcutaneous nodules, he had been diagnosed with neurofibromatosis type 1, the same as his father, sister, and daughter. Computed tomography and magnetic resonance imaging demonstrated an intrasellar mass lesion with a cystic portion in the suprasellar region. Endocrinologically, almost all of his basic hormone levels were normal. A right front-temporal craniotomy was performed for a preoperative diagnosis of craniopharyngioma, and total intracapsular tumor extirpation was achieved. The histological diagnosis was clinically silent corticotroph pituitary adenoma. Neurofibromatosis is sometimes associated with neoplasms of the central nervous system, usually optic gliomas. Associations between pituitary adenomas and NF 1 are very rare and have been reported in only four cases, including the present case.
报告了一例与1型神经纤维瘤病相关的垂体腺瘤病例。2000年6月6日,一名49岁男性因双颞侧偏盲入住冈山大学医院神经外科。29年前,他曾因左侧腹股沟肿瘤接受手术,术后病理证实为神经纤维瘤。基于其存在咖啡斑和皮下结节等其他表现,他被诊断为1型神经纤维瘤病,与他的父亲、姐姐和女儿相同。计算机断层扫描和磁共振成像显示鞍内有一肿块病变,鞍上区域有囊性部分。内分泌方面,他几乎所有的基础激素水平均正常。为术前诊断颅咽管瘤进行了右额颞开颅手术,并实现了肿瘤囊内全切。组织学诊断为临床无功能的促肾上腺皮质激素细胞垂体腺瘤。神经纤维瘤病有时与中枢神经系统肿瘤相关,通常为视神经胶质瘤。垂体腺瘤与1型神经纤维瘤病之间的关联非常罕见,仅报道过4例,包括本病例。