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垂体腺瘤合并神经组织迷离瘤:2例罕见病例报告

Pituitary adenoma with neuronal choristoma: a report of two rare cases.

作者信息

Sharma M C, Karak A K, Mahapatra A K, Sarkar C

机构信息

Department of Pathology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi.

出版信息

Clin Neurol Neurosurg. 1999 Jun;101(2):128-32. doi: 10.1016/s0303-8467(99)00018-9.

Abstract

Two rare cases of pituitary adenoma with neuronal choristoma are described. Both patients were female and presented with features of acromegaly with elevated growth hormone and prolactin levels. Radiologically, both lesions were predominantly intrasellar in location with extension into suprasellar region, but hypothalamus was not involved. Histopathological examination revealed a mixture of chromophobe pituitary adenoma cells and neuronal cells. In both cases, the adenoma component was positive for growth hormone and prolactin. Interestingly, immunopositivity for alpha-subunit, cytokeratin and prolactin was seen in the adenoma and neuronal cells in one case. Our findings support the hypothesis that the neuronal cells possibly arise from adenoma cells as a result of metaplasia.

摘要

本文描述了两例伴有神经组织错构瘤的垂体腺瘤罕见病例。两名患者均为女性,表现为肢端肥大症特征,生长激素和催乳素水平升高。影像学检查显示,两个病变主要位于鞍内,并延伸至鞍上区域,但未累及下丘脑。组织病理学检查发现嫌色性垂体腺瘤细胞和神经细胞混合存在。在两例病例中,腺瘤成分的生长激素和催乳素均呈阳性。有趣的是,在其中一例病例中,腺瘤和神经细胞的α亚基、细胞角蛋白和催乳素均呈免疫阳性。我们的研究结果支持这样一种假说,即神经细胞可能是化生的结果,由腺瘤细胞产生。

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