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[垂体腺瘤结构与功能新知识的实用价值]

[Practical value of new knowledge on the structure and function of pituitary adenomas].

作者信息

Landolt A M

出版信息

Schweiz Med Wochenschr. 1978 Oct 7;108(40):1521-35.

PMID:212827
Abstract

The usual classification of pituitary adenomas into eosinophilic, basophilic, and chromophobe types is no longer sufficient to correlate the histologic findings with the increasing number of clinical syndromes described in recent years. Some histologic forms are observed in several clinical syndromes, whereas some clinical entities may be caused by several histologic types. A new classification is mandatory. Recent endocrine, ultrastructural and histo-immunologic research has shown that the endocrine inactive adenoma, which has usually been related to the "chromophobe" adenoma, represents only a small group of the pituitary neoplasms. A more critical evaluation shows that 3 out of 4 patients present clinical or endocrine signs and findings of increased hormone secretion. Several authors have therefore suggested that pituitary adenomas be classified according to their secretory characteristics, which can be determined either by clinical and endocrine examination or by immunohistology and electron microscopy. Abnormally increased hormone secretion allows early detection of the neoplasm when the remaining normal gland is still able to recover its normal function and the endocrine symptoms therefore are fully reversible. The therapy of pituitary adenomas must normalize the hormone hypersecretion without causing new endocrine deficits, and must at the same time reverse neurological compression symptoms. The treatment may be either surgical excision, irradiation, medical inhibition of abnormal secretion, substitution of insufficient hormones or a combination of these methods. The prognosis of the endocrine symptoms is significantly better in small adenomas and full restoration of sexual function is even observed in an increasing number of patients.

摘要

垂体腺瘤通常分为嗜酸性、嗜碱性和嫌色细胞型,这种分类已不足以将组织学发现与近年来描述的越来越多的临床综合征联系起来。一些组织学形式见于多种临床综合征,而一些临床实体可能由多种组织学类型引起。必须要有新的分类。最近的内分泌、超微结构和组织免疫研究表明,通常与“嫌色细胞”腺瘤相关的内分泌无活性腺瘤仅占垂体肿瘤的一小部分。更严格的评估显示,四分之三的患者出现临床或内分泌体征以及激素分泌增加的表现。因此,几位作者建议根据垂体腺瘤的分泌特征进行分类,这可以通过临床和内分泌检查或免疫组织学和电子显微镜来确定。当剩余的正常腺体仍能恢复其正常功能且内分泌症状因此完全可逆时,激素分泌异常增加可使肿瘤早期被发现。垂体腺瘤的治疗必须使激素分泌过多恢复正常,同时不引起新的内分泌缺陷,并且必须同时缓解神经压迫症状。治疗方法可以是手术切除、放疗、药物抑制异常分泌、补充不足的激素或这些方法的联合使用。小腺瘤的内分泌症状预后明显较好,越来越多的患者甚至出现性功能完全恢复。

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