Dahl I
Acta Pathol Microbiol Scand A. 1977 Nov;85(6):812-8. doi: 10.1111/j.1699-0463.1977.tb03896.x.
A clinical and light microscopic study of 11 patients with ancient neurilemmoma is presented. Ancient neurilemmoma is a cellular form of ordinary neurilemmoma, showing nuclear polymorphism and hyperchromasia. Seven patients were female and 4 were male; their ages ranged between 37 years and 81 years, with a median of 59 years. Seven tumours were 2.5 cm or larger in the widest diameter, and had been slowly enlarging for one year or more. All tumours were solitary, encapsulated showing nuclear polymorphism and hyperchromasia without any mitotic activity. The differential diagnosis is discussed. Follow-up information available on all patients confirmed that the clinical course is benign.
本文对11例陈旧性神经鞘瘤患者进行了临床及光镜研究。陈旧性神经鞘瘤是普通神经鞘瘤的一种细胞形态,表现为核多形性和核深染。7例为女性,4例为男性;年龄在37岁至81岁之间,中位数为59岁。7个肿瘤最大直径为2.5 cm或更大,且已缓慢增大一年或更长时间。所有肿瘤均为单发,有包膜,表现为核多形性和核深染,无任何有丝分裂活性。文中讨论了鉴别诊断。所有患者的随访信息证实临床病程为良性。