Kleinman G M, Schoene W C, Walshe T M, Richardson E P
J Neurosurg. 1978 Jul;49(1):111-8. doi: 10.3171/jns.1978.49.1.0111.
The authors give follow-up information on Case 59 of Cushing's 1931 series of cerebellar astrocytomas. The patient died with a malignant cerebellar astrocytoma 48 years after partial removal of a previously benign astrocytoma at the same site. Including the present one, there have been only five reported cases in which this has occurred. Ordinarily, juvenile pilocytic astrocytomas are of extremely genign character, and it is well established that even with incomplete resections patients have survived for years without progression of the tumor. Not all of the cases so reported can be wholly accepted as respresenting malignant transformation of the tumor, but may instead be instances of recurrence of an inherently benign glioma since the presence of features such as endothelial hyperplasia or nuclear atypicality in a juvenile pilocytic astrocytoma does not warrant is being classified as malignant. Features truly suggestive of malignancy are hypercellularity, frequent mitoses, necrosis, and, in some instances, a diffusely infiltrative growth pattern; all of these features were found in the present case.
作者提供了库欣1931年系列小脑星形细胞瘤病例59的随访信息。该患者在同一部位先前的良性星形细胞瘤部分切除48年后死于恶性小脑星形细胞瘤。包括本病例在内,仅有5例此类情况的报道。通常,青少年毛细胞型星形细胞瘤具有极低的恶性特征,而且即使切除不完全,患者也能存活数年而肿瘤不进展,这一点已得到充分证实。并非所有如此报道的病例都能完全被视为肿瘤发生了恶性转化,而可能是原本良性的胶质瘤复发,因为青少年毛细胞型星形细胞瘤中出现内皮细胞增生或核异型性等特征并不足以将其归类为恶性。真正提示恶性的特征是细胞增多、频繁的有丝分裂、坏死,在某些情况下还有弥漫性浸润性生长模式;本病例中发现了所有这些特征。