摘要
目的探讨垂体细胞增生的诊断与治疗。方法男性2例,女性42例,平均年龄28.7岁,平均病程2.4年。临床表现和内分泌检查符合闭经泌乳综合征13例,库欣综合征11例,巨人症1例,无内分泌功能紊乱19例。蝶鞍MRI正常3例,垂体上缘膨隆30例,蝶鞍内信号不均匀26例,垂体柄偏斜17例。44例均行经口鼻蝶窦显微外科垂体探查术。结果44例术后病理均为垂体前叶细胞增生,随访3个月至5年。闭经泌乳患者术后改善12例,复发1例。库欣综合征患者术后改善8例,稳定1例,复发2例。巨人症患者术后无改善。无内分泌功能紊乱症状患者术后改善14例。结论垂体细胞增生在术前很难明确诊断,手术疗效较垂体腺瘤差,易复发。
Objective To discuss the diagnosis and treatment of the pituitary hyperplasia. Methods Among the 44 patients with pituitary hyperplasia, 2 cases were male and 42 were female. Mean age was 28. 7 yrs old and mean history was 2. 4 years. Among them, 13 ( 29. 5% ) had amenorrhea-galactorrhea syndrome, 11 (25%) had Cushing's syndrome, 1 (2.3%) had gigantism, and 19 (43.2%) didn't have symptoms of endocrine disturbance. MRI showed normal in 3 cases, increase of the height of pituitary in 30 cases, hypointensity on Tl-weighted images in 26 cases, and deviation of the pituitary pedicle in 17 cases. All patients underwent trans-spheniod hypophysectomy. Results Pathology showed pituitary hyperplasia in all 44 cases. Postoperative follow-up were 3 months to 5 years. Among 13 amenorrhea-galactorrhea syndrome, 12 improved, 1 recurred. Among 11 Cushing's syndrome, 8 improved, 1 stabled, 2 recurred. 1 gigantism didn't improve. Among 19 other non-endocrine symptoms, 14 improved. Conclusion Preoperation diagnosis of pituitary hyperplasia was difficult. The effect of hypophysectomy and the prognosis were not as good as pituitary adenoma.
出处
《中华神经外科杂志》
CSCD
北大核心
2007年第6期432-434,共3页
Chinese Journal of Neurosurgery