Iizuka H, Nojima T, Kadoya S
Department of Neurosurgery, Kanazawa Medical University.
Noshuyo Byori. 1996 Nov;13(2):95-8.
This report concerns the unusual case of a germinoma primarily arising from the right optic nerve. The patient is a 31-year-old male who presented with progressive loss of vision, but with no clinical evidence suggestive of hypothalamic-pituitary dysfunction, including diabetes insipidus. The neuroimaging studies disclosed a tumor in the right optic nerve, but no intracranial tumors. Histologically, the tumor consisted of proliferating large clear cells with lymphocytic infiltration. The immunohistochemical studies revealed that the tumor cells expressed placental alkaline phosphatase. Perusal of the literature revealed that germinomas arising from the optic nerve have not been described heretofore. The histogenesis of the optic nerve germinoma is considered in relation to the proposed theory on the genesis of intracranial germ cell tumors.
本报告涉及一例罕见的主要起源于右侧视神经的生殖细胞瘤病例。患者为一名31岁男性,表现为进行性视力丧失,但无临床证据提示下丘脑 - 垂体功能障碍,包括尿崩症。神经影像学研究显示右侧视神经有肿瘤,但无颅内肿瘤。组织学上,肿瘤由增生的大透明细胞和淋巴细胞浸润组成。免疫组化研究显示肿瘤细胞表达胎盘碱性磷酸酶。查阅文献发现,此前尚未有起源于视神经的生殖细胞瘤的描述。结合颅内生殖细胞肿瘤发生的理论,对视神经生殖细胞瘤的组织发生进行了探讨。