Tyson D, Reggiardo D, Sklar C, David R
Department of Pediatrics, New York University Medical Center, New York 10016.
Am J Dis Child. 1993 Oct;147(10):1057-61. doi: 10.1001/archpedi.1993.02160340043011.
To report five cases of prolactin (PRL)-secreting macroadenomas in adolescents, including their presentations and responses to bromocriptine mesylate treatment.
Five adolescents (three females and two males) aged between 12.5 and 17 years were diagnosed as having PRL-secreting macroadenomas at the pediatric endocrine service at New York University Medical Center between 1987 and 1989. Presenting complaints included visual field deficits, gynecomastia, and amenorrhea, both primary and secondary. All patients demonstrated some feature of hypogonadism or pubertal arrest. Diagnostic criteria included an elevated serum PRL level (mean, 1670 micrograms/L; range, 610 to 3700 micrograms/L) and visualization of a pituitary tumor that measured greater than 1 cm by either a computed tomographic scan or magnetic resonance imaging (mean size, 2.7 cm; range, 1.4 to 4 cm).
Each patient was treated with bromocriptine mesylate at an oral dose of 7.5 mg/d. The patients continued with that treatment for the duration of the study period.
Anterior pituitary function was evaluated in four of five patients before treatment. All four were growth hormone deficient. Three patients were also gonadotropin deficient. Thyrotropin (thyroid-stimulating hormone) and corticotropin (adrenocorticotropic hormone) deficiencies were demonstrated in three patients who had multiple pituitary deficits. Follow-up testing included serial PRL measurements and radiographic imaging of tumor size. All patients demonstrated a marked decrease in PRL levels, as well as in tumor size (mean shrinkage, 70%). The three patients who initially had visual field deficits showed significant improvement of vision with bromocriptine therapy. Follow-up study of anterior pituitary function showed significant improvement with bromocriptine treatment in three patients.
Bromocriptine was quite effective in the shrinkage of PRL-secreting macroadenomas in all our patients. It is a noninvasive treatment that can preserve and restore vision, as well as pituitary function, which is integral to continued growth and sexual maturation of the adolescent. Bromocriptine is preferable to surgery or radiation in the treatment of PRL-secreting macroadenomas in the adolescent.
报告5例青少年催乳素(PRL)分泌型大腺瘤病例,包括其临床表现及对甲磺酸溴隐亭治疗的反应。
1987年至1989年间,纽约大学医学中心儿科内分泌科诊断出5名年龄在12.5至17岁之间的青少年(3名女性和2名男性)患有PRL分泌型大腺瘤。主要症状包括视野缺损、男性乳房发育以及原发性和继发性闭经。所有患者均表现出性腺功能减退或青春期停滞的某些特征。诊断标准包括血清PRL水平升高(平均1670微克/升;范围610至3700微克/升),以及通过计算机断层扫描或磁共振成像显示垂体肿瘤直径大于1厘米(平均大小2.7厘米;范围1.4至4厘米)。
每位患者均接受口服甲磺酸溴隐亭治疗,剂量为7.5毫克/天。在研究期间,患者持续接受该治疗。
5名患者中有4名在治疗前接受了垂体前叶功能评估。所有4名患者均生长激素缺乏。3名患者还存在促性腺激素缺乏。3名存在多种垂体功能缺陷的患者表现出促甲状腺激素和促肾上腺皮质激素缺乏。随访检查包括连续PRL测量和肿瘤大小的影像学检查。所有患者的PRL水平以及肿瘤大小均显著下降(平均缩小70%)。最初有视野缺损的3名患者在接受溴隐亭治疗后视力有显著改善。垂体前叶功能的随访研究显示,3名患者在接受溴隐亭治疗后有显著改善。
溴隐亭对我们所有患者的PRL分泌型大腺瘤缩小非常有效。它是一种非侵入性治疗方法,可保留并恢复视力以及垂体功能,而垂体功能对于青少年的持续生长和性成熟至关重要。在青少年PRL分泌型大腺瘤的治疗中,溴隐亭优于手术或放疗。