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具有不典型组织学特征的垂体细胞瘤。

Pituicytoma with unusual histological features.

机构信息

Department of Pathology, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Seoul, South Korea.

出版信息

Pathol Int. 2011 Oct;61(10):598-602. doi: 10.1111/j.1440-1827.2011.02708.x. Epub 2011 Aug 4.

DOI:10.1111/j.1440-1827.2011.02708.x
PMID:21951670
Abstract

Pituicytoma is a rare low-grade glial neoplasm that originates in the neurohypophysis or infundibulum. Because of its rare occurrence, the morphology and differentiation of pituicytoma have not been fully clarified. Here, we report a case of pituicytoma with unusual histological features mimicking ependymoma, but exhibiting the diverse morphology and differentiation of pituicytoma. The 1.4 cm-sized suprasellar mass was incidentally found in the magnetic resonance image of a 42-year-old Korean woman who had had a traffic accident. Four years later, she presented with symptoms of hypopituitarism and the follow-up images revealed slight enlargement of the mass. After gross total resection, microscopic examination revealed oval to elongated cells with abundant eosinophilic cytoplasm arranged in a perivascular pseudorosette pattern and short interlacing fascicles. Pleomorphic tumor cells and Herring bodies were diffusely distributed within the tumor. Neither Rosenthal fibers nor eosinophilic granular bodies were identified. The tumor cells were immunohistochemically positive for glial fibrillary acidic protein, vimentin and S-100 protein, but negative for synaptophysin and adenohypophyseal hormones. The epithelial membrane antigen and CD99 were expressed with a paranuclear dot-like or membranous pattern in some tumor cells. Ultrastructural examination revealed that the tumor cells with intermediate filaments were closely apposed with intercellular junctions and frequent basal lamina production.

摘要

垂体细胞瘤是一种起源于神经垂体或漏斗的罕见低级别神经胶质瘤。由于其罕见性,垂体细胞瘤的形态和分化尚未完全阐明。在此,我们报告一例具有不典型组织学特征的垂体细胞瘤,类似于室管膜瘤,但表现出垂体细胞瘤的多种形态和分化。一位 42 岁的韩国女性因交通事故行磁共振成像检查时偶然发现 1.4cm 大小的鞍上肿块,4 年后出现垂体功能减退症状,随访图像显示肿块略有增大。大体全切除后,显微镜下观察到肿瘤内排列呈血管周围假玫瑰花结样和短交织束状的椭圆形至长形细胞,具有丰富的嗜酸性细胞质。多形性肿瘤细胞和 Herring 小体弥漫分布于肿瘤内。未见 Rosenthal 纤维和嗜酸性颗粒小体。肿瘤细胞免疫组化显示胶质纤维酸性蛋白、波形蛋白和 S-100 蛋白阳性,突触素和腺垂体激素阴性。上皮膜抗原和 CD99 在一些肿瘤细胞中呈核周点状或膜状表达。超微结构检查显示,具有中间丝的肿瘤细胞紧密贴合,细胞间连接频繁,基底膜产生频繁。

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