Cerda-Nicolas M, Kepes J J
Department of Pathology, Faculty of Medicine, University of Valencia, Spain.
Acta Neuropathol. 1993;85(4):349-61. doi: 10.1007/BF00334444.
The presence of connective tissue elements in gliomas necessitates in every case a thorough analysis of the character and derivation of such elements to allow the formulation of an appropriate diagnosis. Four cases are presented in this paper. In cases 1 and 2 (anaplastic astrocytomas in two children, 9 and 4 years old, respectively) all the neoplastic elements were astrocytes and their ability to produce or indirectly promote the production of reticulin and collagen fibers accounted for the presence of such elements in close association with the tumor cells. The term "gliofibroma" has been coined for such tumors, but "desmoplastic astrocytoma", (low grade or anaplastic) or in highly malignant cases "desmoplastic glioblastoma", as the case may be, also seem to be appropriate terms for such neoplasms. In contrast, cases 3 and 4 represented composite tumors in adults (66 and 58 years old, respectively) and the neoplasms of these patients consisted of glioblastoma and sarcoma, the latter component demonstrably being of vascular origin. This is the type of tumor usually referred to as gliosarcoma or "Feigin tumor". Although some apparent similarities between the two groups may exist at times, the histogenesis of the latter group's sarcomatous or sarcoma-like portions is different from that of the first group and, therefore, warrants separate diagnostic terms and placement in brain tumor classification.
胶质瘤中结缔组织成分的存在,使得在每种情况下都必须对这些成分的特征和来源进行全面分析,以便做出恰当的诊断。本文介绍了4个病例。在病例1和病例2中(分别为两名儿童,年龄为9岁和4岁的间变性星形细胞瘤),所有肿瘤成分均为星形胶质细胞,它们产生或间接促进网状纤维和胶原纤维生成的能力,解释了这些成分与肿瘤细胞紧密相关的原因。已经为这类肿瘤创造了“胶质纤维瘤”这一术语,但“促结缔组织增生性星形细胞瘤”(低级别或间变性),或者在高度恶性的病例中,视情况而定的“促结缔组织增生性胶质母细胞瘤”,似乎也是这类肿瘤的合适术语。相比之下,病例3和病例4代表成人(分别为66岁和58岁)的复合性肿瘤,这些患者的肿瘤由胶质母细胞瘤和肉瘤组成,后者成分显然起源于血管。这就是通常被称为胶质肉瘤或“费金瘤”的肿瘤类型。尽管两组之间有时可能存在一些明显的相似之处,但后一组肉瘤样或肉瘤部分的组织发生与第一组不同,因此,需要有单独的诊断术语,并在脑肿瘤分类中进行归类。