Schwartz A M, Ghatak N R, Laine F J
Department of Pathology, Medical College of Virginia, Richmond 23298.
Clin Neuropathol. 1990 Mar-Apr;9(2):55-9.
An infant with bilateral familial retinoblastomas was found at age 6 months to have a large mass within the region of the sella turcica. The histology, immunoreactivity and ultrastructure of the tumor showed primitive neuroectodermal cells. A small number of cells showed positive immunostaining to retinal S antigen. This represents a rare form of so-called trilateral retinoblastoma. In most cases of trilateral retinoblastoma, the intracranial non-metastatic tumor is within the pineal gland. The occurrence of such a tumor in the region of sella turcica is very unusual and its possible significance is discussed in regard to our current understanding of the susceptibility to carcinogenesis conferred by inheritance of the mutant retinoblastoma gene, Rb-1.
一名患有双侧家族性视网膜母细胞瘤的婴儿在6个月大时被发现蝶鞍区域有一个大肿块。肿瘤的组织学、免疫反应性和超微结构显示为原始神经外胚层细胞。少数细胞对视网膜S抗原呈阳性免疫染色。这代表了一种罕见的所谓三边性视网膜母细胞瘤形式。在大多数三边性视网膜母细胞瘤病例中,颅内非转移性肿瘤位于松果体。这种肿瘤出现在蝶鞍区域非常罕见,本文结合我们目前对由突变视网膜母细胞瘤基因Rb-1遗传所赋予的致癌易感性的理解,讨论了其可能的意义。