Dysplastic Gangliocytoma: A Rare Example of Cerebellar Tumor with An Evident Genetic Profile (Cowden Syndrome)

J. O. Rodríguez-Parets, Luis Miguel Chinchilla Tábora, Enrique Montero Mateos, E. M. Torres, M. Cruz
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引用次数: 0

Abstract

Objective: To describe the histological and immunohistochemical findings observed when studying a dysplastic cerebellar gangliocytoma observed in a 33-year-old man with a history of Thyroid Cancer. Material and Methods: Radiological images (MRI) and histological and immunohistochemical preparations obtained from the cerebellar tissue were received in our laboratory. Results: A neoplasm constituted by aberrant-looking mature neurons was observed that showed negativity for the immunohistochemical markers of the PTEN protein, expression of the activity of the PTEN gene. Conclusions: Verify the diagnosis of a rare entity, clearly related in scientific publications with Cowden’s Syndrome.
发育不良神经节细胞瘤:一例具有明显遗传特征的罕见小脑肿瘤(考登综合征)
目的:描述在研究一名33岁有甲状腺癌病史的男性小脑神经节细胞瘤的组织学和免疫组织化学结果。材料和方法:在我们的实验室接受了小脑组织的放射学图像(MRI)和组织学和免疫组织化学准备。结果:观察到由外观异常的成熟神经元构成的肿瘤,PTEN蛋白免疫组化标记物、PTEN基因活性表达均呈阴性。结论:证实了一个罕见的实体的诊断,在科学出版物与考登综合征明确相关。
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