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[鞍区神经内分泌联合肿瘤]

[Combined neuronal and endocrine tumors of the sellar region].

作者信息

Saeger W, Lüdecke D K, Losa M

机构信息

Institut für Pathologie, Marienkrankenhauses Hamburg.

出版信息

Pathologe. 1997 Nov;18(6):419-24. doi: 10.1007/s002920050236.

Abstract

Gangliocytomas or gangliogliomas of the sellar region are very rare tumors. In a great proportion of those cases an adenoma of the anterior pituitary develops from the cell type that is hyperstimulated by the releasing hormone produced from the gangliocytoma. Five GHRH secreting gangliocytomas are reported. Four of these were localized adjacent to a GH secreting adenoma. In one case, no adenoma tissue was found beside the ganglicytoma. As only the adenomas can secrete GH, the adenomas and not the gangliocytomas are directly responsible for acromegaly so that such an adenoma has to be present in cases of acromegaly. A CRH secreting gangliocytoma was combined with an ACTH cell adenoma that had induced Cushing's disease. A ganglioglioma of the posterior pituitary had led to an inappropriate secretion of Vasopressin. The morphology of the different tumors is presented.

摘要

鞍区神经节细胞瘤或神经节胶质瘤是非常罕见的肿瘤。在这些病例中,很大一部分垂体前叶腺瘤由神经节细胞瘤产生的释放激素过度刺激的细胞类型发展而来。报告了5例分泌生长激素释放激素(GHRH)的神经节细胞瘤。其中4例位于分泌生长激素(GH)的腺瘤附近。在1例中,神经节细胞瘤旁未发现腺瘤组织。由于只有腺瘤能分泌GH,所以腺瘤而非神经节细胞瘤直接导致肢端肥大症,因此肢端肥大症患者必须存在这样的腺瘤。1例分泌促肾上腺皮质激素释放激素(CRH)的神经节细胞瘤与诱发库欣病的促肾上腺皮质激素(ACTH)细胞腺瘤合并。垂体后叶的神经节胶质瘤导致了抗利尿激素的不适当分泌。介绍了不同肿瘤的形态。

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