Tajika Y, Kubo O, Takeshita M, Tajika T, Shimizu T, Kitamura K
Department of Neurosurgery, Tokyo Women's Medical College.
No Shinkei Geka. 1989 Dec;17(12):1181-6.
The authors report a rare case of collision tumor composed of intrasellar gangliocytoma and pituitary adenoma. The patient was a 56-year-old woman, who had a mild acromegalic feature and slightly elevated plasma GH level. But she had no abnormal neurological findings. Transsphenoidal microsurgery was performed and an intrasellar tumor was totally removed. After the operation, plasma GH level decreased to within normal level. She was discharged with no neurological deficit. Histological examination showed two components. One of them was gangliocytoma composed of many large, and often binucleated cells with Nissl substance. The other had the appearance of chromophobe adenoma. In this part, some of the cells showed positive stain for GH. The clinical and histological features of this lesion are discussed and compared with 31 other cases of intrasellar ganglioglioma or gangliocytoma.
作者报告了一例罕见的由鞍内神经节细胞瘤和垂体腺瘤组成的碰撞瘤病例。患者为一名56岁女性,有轻度肢端肥大症特征,血浆生长激素(GH)水平略有升高。但她没有异常的神经系统表现。进行了经蝶窦显微手术,鞍内肿瘤被完全切除。术后,血浆GH水平降至正常范围内。她出院时没有神经功能缺损。组织学检查显示有两个成分。其中之一是神经节细胞瘤,由许多大的、通常为双核且含有尼氏体的细胞组成。另一个具有嫌色性腺瘤的外观。在这部分中,一些细胞对GH呈阳性染色。本文讨论了该病变的临床和组织学特征,并与其他31例鞍内神经节胶质瘤或神经节细胞瘤病例进行了比较。