Santos Antonio Benigno A, França Mariana M, Hirosawa Renata M, Marivo Mônica, Zanini Marco A, Nunes Vania S
Department of Clinical Medicine, Botucatu Medical School, Universidade Estadual Paulista, SP, Brazil.
Arq Bras Endocrinol Metabol. 2011 Jun;55(5):345-8. doi: 10.1590/s0004-27302011000500008.
Pituitary tumor apoplexy is a rare neuroendocrine syndrome resulting, in most cases, from hemorrhage or infarctation of a pre-existing pituitary adenoma. Treatment recommendations vary; some authors advocate urgent surgical decompression of the tumor, whereas others suggest that conservative management can lead to recovery of neuro-ophthalmologic function. We describe two patients with pituitary tumor apoplexy who had clinically non-functioning macroadenomas and hypopituitarism, including hypogonadism. They were treated conservatively without surgery, and achieved tumor remission.
垂体瘤卒中是一种罕见的神经内分泌综合征,在大多数情况下,由先前存在的垂体腺瘤出血或梗死引起。治疗建议各不相同;一些作者主张对肿瘤进行紧急手术减压,而另一些人则认为保守治疗可使神经眼科功能恢复。我们描述了两名患有垂体瘤卒中的患者,他们患有临床上无功能的大腺瘤和垂体功能减退,包括性腺功能减退。他们接受了非手术保守治疗,并实现了肿瘤缓解。