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临床综述65. 垂体偶发瘤患者的评估与治疗

Clinical review 65. Evaluation and treatment of the patient with a pituitary incidentaloma.

作者信息

Molitch M E

机构信息

Center for Endocrinology, Metabolism, and Molecular Medicine, Northwestern University Medical School, Chicago, Illinois 60611.

出版信息

J Clin Endocrinol Metab. 1995 Jan;80(1):3-6. doi: 10.1210/jcem.80.1.7829630.

DOI:10.1210/jcem.80.1.7829630
PMID:7829630
Abstract

Incidental pituitary adenomas are being found commonly with our improved neuroradiological imaging procedures. Screening for hormone oversecretion by these tumors appears to be warranted. For patients with macroadenomas, patients should also be screened for hypopituitarism. In the absence of visual field abnormalities or hypothalamic/stalk compression, it may be appropriate to observe such patients carefully with repeated CT or MRI scans. A limited amount of data suggests that significant tumor enlargement will occur in less than 15% of patients with microadenomas (7). However, all macroadenomas must start out as microadenomas, so periodic follow-up is indicated to assess this possibility. Macroadenomas, by their very existence at the time of detection, have already indicated a propensity for growth. Over the limited period of follow-up in the two series reported, significant growth occurred in almost one third of patients with macroadenomas (7, 8). Hemorrhage into such tumors is uncommon, but anticoagulation may predispose to this complication. When there is no evidence of visual field deficits, an attempt at medical therapy with a dopamine agonist is reasonable, realizing that only about 10% of such patients will respond with a decrease in tumor size. Surgery is indicated if there is evidence of tumor enlargement, especially when such growth is accompanied by compression of the optic chiasm, cavernous sinus invasion, or the development of pituitary hormone deficiencies.

摘要

随着神经放射成像技术的改进,偶然发现的垂体腺瘤越来越常见。对这些肿瘤进行激素分泌过多的筛查似乎是必要的。对于患有大腺瘤的患者,还应筛查垂体功能减退。在没有视野异常或下丘脑/垂体柄受压的情况下,通过重复CT或MRI扫描仔细观察此类患者可能是合适的。有限的数据表明,微腺瘤患者中不到15%会出现明显的肿瘤增大(7)。然而,所有大腺瘤最初都必定是微腺瘤,因此需要定期随访以评估这种可能性。大腺瘤在被发现时的存在本身就已经表明有生长的倾向。在所报道的两个系列的有限随访期内,几乎三分之一的大腺瘤患者出现了明显的生长(7, 8)。此类肿瘤出血并不常见,但抗凝治疗可能会引发这种并发症。当没有视野缺损的证据时,尝试使用多巴胺激动剂进行药物治疗是合理的,但要意识到只有约10%的此类患者会出现肿瘤缩小。如果有肿瘤增大的证据,特别是当这种生长伴有视交叉受压、海绵窦侵犯或垂体激素缺乏的发生时,就需要进行手术治疗。

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