Ono N, Nakamura M, Inoue H K, Tamura M, Murata M
Department of Neurosurgery, Gunma University School of Medicine, Japan.
Childs Nerv Syst. 1990 Nov;6(7):416-20. doi: 10.1007/BF00302231.
A mixed glioma and sarcoma in a 3-month-old infant is presented as a rare case of gliosarcoma with a good response to treatment. This congenital case is quite different from those in adults: the tumor cells were mainly composed of sarcomatous elements; glial components were not anaplastic without obvious endothelial hyperplasia, but presented as reticulin-free islands, mimicking a reactive glioma in a sarcoma. It may be termed "sarcoglioma" to distinguish from a classic gliosarcoma. The origin of the rare mixed tumor may be related to a dysgenesis of both mesenchymal and glial elements.
本文报告了一例3个月大婴儿的混合性胶质瘤和肉瘤,这是一例罕见的胶质肉瘤,对治疗反应良好。这个先天性病例与成人病例有很大不同:肿瘤细胞主要由肉瘤成分组成;胶质成分无间变,无明显内皮细胞增生,而是呈无网状纤维的岛状,类似肉瘤中的反应性胶质瘤。为与经典的胶质肉瘤相区分,可将其称为“肉瘤样胶质瘤”。这种罕见混合性肿瘤的起源可能与间充质和胶质成分的发育异常有关。