Kasantikul V, Palmer J O, Netsky M G, Glasscock M E, Hays J W
Arch Otolaryngol. 1980 Aug;106(8):456-9. doi: 10.1001/archotol.1980.00790320008003.
We report a case of astrocytoma of the acoustic nerve. Most gliomas arise from the brainstem, and seldom originate in the acoustic or other "true" cranial and spinal nerves. Clinical features of this rare acoustic tumor differ from those of brainstem gliomas, but are indistinguishable from typical acoustic neurilemoma. We discuss the diagnosis and histogenesis of glioma arising in the eighth cranial nerve. Demonstration of glial fibrillary acid protein, an antigen specific for astrocytes, is a new method of verifying the diagnosis. Review of the literature indicates that a few cases of epithelial-like tumors of peripheral nerves may have been of neuroepithelial origin. The evidence, however, generally is not sufficient to exclude the possibility of metastatic neoplasms or other tumors such as malignant schwannoma and melanoma. Most of these putative gliomas contained gland-like tissue, and did not have the morphologic appearance of astrocytoma, as in approximately five reported examples, and in our case.
我们报告一例听神经星形细胞瘤。大多数胶质瘤起源于脑干,很少起源于听神经或其他“真正的”颅神经和脊神经。这种罕见的听神经肿瘤的临床特征与脑干胶质瘤不同,但与典型的听神经鞘瘤难以区分。我们讨论了起源于第八颅神经的胶质瘤的诊断和组织发生。胶质纤维酸性蛋白(一种星形胶质细胞特异性抗原)的检测是验证诊断的新方法。文献回顾表明,少数周围神经上皮样肿瘤可能起源于神经上皮。然而,证据通常不足以排除转移性肿瘤或其他肿瘤(如恶性神经鞘瘤和黑色素瘤)的可能性。这些所谓的胶质瘤大多含有腺样组织,并不具有星形细胞瘤的形态学表现,如大约五个已报道的病例以及我们的病例所示。