Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Hum Pathol. 2010 Mar;41(3):443-6. doi: 10.1016/j.humpath.2009.08.017. Epub 2009 Dec 1.
Primary central nervous system tumors with signet-ring morphology are exceedingly rare. We report an unusual case of glioblastoma with signet-ring cell features in an 81-year-old woman. Microscopic examination revealed a highly anaplastic tumor, with a prominent proportion of tumor cells exhibiting signet-ring appearance characterized by classic round cytoplasmic inclusions and eccentrically positioned nuclei. The tumor cells were immunoreactive for glial fibrillary acidic protein and S100, and negative for cytokeratins, confirming their glial origin. Ultrastructurally, the tumor cells were noted to contain intermediate filaments, and by fluorescence in-situ hybridization analysis, they demonstrated intact 1p/19q. The presence of signet-ring cells in the central nervous system should immediately raise the suspicion of metastatic carcinoma, particularly from the upper gastrointestinal tract. In the present case, however, the morphological and immunohistochemical features were diagnostic of a malignant primary glial neoplasm (glioblastoma). This case highlights the diagnostic difficulties that can arise in such instances, given the rarity of signet-ring morphology in primary central nervous system tumors.
原发中枢神经系统具有印戒细胞形态的肿瘤极其罕见。我们报告了一例 81 岁女性具有印戒细胞特征的胶质母细胞瘤的不典型病例。显微镜检查显示为高度间变肿瘤,其中相当比例的肿瘤细胞呈现出典型的圆形胞质内包涵体和偏心性核的印戒外观。肿瘤细胞对胶质纤维酸性蛋白和 S100 呈免疫反应性,而对细胞角蛋白呈阴性,证实其为神经胶质起源。超微结构检查发现肿瘤细胞含有中间丝,荧光原位杂交分析显示 1p/19q 完整。中枢神经系统中出现印戒细胞应立即怀疑转移性癌,特别是来自上消化道的癌。然而,在本例中,形态学和免疫组化特征诊断为恶性原发性神经胶质肿瘤(胶质母细胞瘤)。鉴于原发中枢神经系统肿瘤中出现印戒细胞形态非常罕见,这种情况突出了在这种情况下可能出现的诊断困难。