Katsetos C D, Burger P C
Department of Pathology, Hahnemann University, Philadelphia, PA 19102-1192.
Semin Diagn Pathol. 1994 May;11(2):85-97.
The histogenetic approach to the classification of embryonal tumors of the central nervous system has historically received wide acceptance as a scheme for histologic typing and nosologic definition. Medulloblastoma is a paradigm of a neuroblastic neoplasm whose origins and differentiation potential are traceable to cerebellar embryogenesis. Medulloblastomas show unequivocal neuroblastic maturational changes evidenced by neuritogenesis and expression of neuronal cytoskeletal and other neuronal differentiation-associated antigenic determinants. In addition, ganglion cells form in some lesions. Based on differential patterns of immunoreactivity for calbindin-D28k (a ventricular matrix (VM)-associated neuronal calcium binding protein, which is not expressed in the external granule layer (EGL) or its progeny) and the class III beta-tubulin isotype (beta III) (expressed metachronously in the neuronal descendants of both neuroepithelia), it is possible that distinct subsets of medulloblastomas may implicate clonally-related neuroblasts from two sources: VM for classic medulloblastomas and the EGL for desmoplastic (nodular) medulloblastomas. However, the possibility of two separate origins for the classic medulloblastomas cannot be entirely excluded. Origin from the VM is suggested for the rare subset of medulloblastomas with ganglion cells. It is, however, unclear whether these ganglion cells are neoplastic (products of terminal neuronal differentiation), or dysplastic (entrapped preexisting elements of cerebellar heterotopias). Glial differentiation (gliomatous transformation) in medulloblastomas is at issue but is documented in rare cases of classic medulloblastomas (presumed heteroclones of cotransformed VM glial precursors), or desmoplastic medulloblastomas (probable stromal glial transformation-induction). Astrocytic proliferations in desmoplastic medulloblastomas may be stroma-derived (neuronal differentiation-associated), analogous to Schwann cell contributions during maturation of peripheral neuroblastomas.
中枢神经系统胚胎性肿瘤的组织发生学分类方法,在历史上作为一种组织学分型和疾病分类定义的方案已被广泛接受。髓母细胞瘤是一种神经母细胞瘤的范例,其起源和分化潜能可追溯到小脑胚胎发育过程。髓母细胞瘤表现出明确的神经母细胞成熟变化,表现为神经突形成以及神经元细胞骨架和其他与神经元分化相关的抗原决定簇的表达。此外,在一些病变中会形成神经节细胞。基于钙结合蛋白-D28k(一种与脑室基质(VM)相关的神经元钙结合蛋白,在外颗粒层(EGL)或其后代中不表达)和III类β-微管蛋白亚型(βIII)(在两种神经上皮的神经元后代中同步表达)的免疫反应性差异模式,有可能不同亚型的髓母细胞瘤可能涉及来自两个来源的克隆相关神经母细胞:经典髓母细胞瘤的VM和促纤维增生性(结节性)髓母细胞瘤的EGL。然而,经典髓母细胞瘤有两个独立起源的可能性不能完全排除。具有神经节细胞的罕见髓母细胞瘤亚群提示起源于VM。然而,尚不清楚这些神经节细胞是肿瘤性的(终末神经元分化产物)还是发育异常的(陷入的小脑异位预先存在的成分)。髓母细胞瘤中的胶质分化(胶质瘤转化)存在争议,但在罕见的经典髓母细胞瘤病例(推测为共转化的VM胶质前体的异源克隆)或促纤维增生性髓母细胞瘤(可能是基质胶质转化诱导)中有记录。促纤维增生性髓母细胞瘤中的星形细胞增殖可能是基质来源的(与神经元分化相关),类似于外周神经母细胞瘤成熟过程中施万细胞的贡献。