Montini M, Pagani G, Gianola D, Pagani M D, Salmoiraghi M, Ferrari L, Lancranjan I
J Clin Endocrinol Metab. 1986 Jul;63(1):266-8. doi: 10.1210/jcem-63-1-266.
Since Corenblum reported in 1975 the first documented reduction of tumor size in two patients with macroprolactinoma, evidence has accumulated that bromocriptine causes shrinkage of PRL-secreting adenomas in most patients. Recently a long-acting form of bromocriptine (bromocriptine LA) was developed. A single dose of 50 mg i.m. decreases basal and sleep-related PRL secretion in normal subjects for 28 days. We treated 13 patients (8 women, 5 men) with PRL secreting tumors (5 macroadenomas and 8 microadenomas) with a single dose (50 mg) of bromocriptine LA. In the 5 patients with macroprolactinomas plasma PRL levels decreased markedly within 12 hours, reaching normal levels in only one patient. In all patients the suppression of PRL secretion lasted at least 28 days and the tumor size was reduced by 20% to 59% within 21 days after the injection. Visual fields improved in all 3 patients with abnormal vision prior to the injection. In one patient with bitemporal hemianopsia an almost normalization of the visual field was noted 24 hours after bromocriptine LA administration. In 7/8 patients with microprolactinomas plasma PRL levels decreased to within the normal range within 12 hours after the administration of bromocriptine LA. The normalization of PRL secretion lasted for at least 28 days. Menses resumed in all 6 women 7 to 41 days after the injection, galactorrhea disappeared in all 4 patients, and libido and potency become normal in both men with microprolactinomas. Patients treated with bromocriptine LA reported only short-lasting (1 hour - 2 days) mild or moderate adverse effects, consisting of dizziness (4 patients) and nausea (4 patients). Long-acting bromocriptine should be considered as the initial management for patients with PRL-secreting tumors. The use of bromocriptine LA could also overcome the compliance problems that occur in many patients soon after the initiation of oral bromocriptine therapy.
自1975年科伦布卢姆报告首例有记录的两名大泌乳素瘤患者肿瘤体积缩小以来,已有越来越多的证据表明,溴隐亭可使大多数泌乳素分泌腺瘤患者的肿瘤缩小。最近研制出了一种长效溴隐亭(长效溴隐亭)。单次肌肉注射50毫克可使正常受试者的基础泌乳素分泌及与睡眠相关的泌乳素分泌在28天内减少。我们用单次剂量(50毫克)的长效溴隐亭治疗了13例泌乳素分泌肿瘤患者(8名女性,5名男性)(5例大腺瘤和8例微腺瘤)。在5例大泌乳素瘤患者中,血浆泌乳素水平在12小时内显著下降,仅1例患者达到正常水平。所有患者的泌乳素分泌抑制至少持续28天,注射后21天内肿瘤大小缩小20%至59%。所有3例注射前视力异常的患者视力均有改善。1例双颞侧偏盲患者在注射长效溴隐亭后24小时视野几乎恢复正常。在8例微泌乳素瘤患者中的7例,血浆泌乳素水平在注射长效溴隐亭后12小时内降至正常范围。泌乳素分泌正常化至少持续28天。所有6名女性在注射后7至41天月经恢复,所有4例患者的溢乳消失,2例微泌乳素瘤男性患者的性欲和性功能恢复正常。接受长效溴隐亭治疗的患者仅报告有短暂(1小时至2天)的轻度或中度不良反应,包括头晕(4例患者)和恶心(4例患者)。长效溴隐亭应被视为泌乳素分泌肿瘤患者的初始治疗方法。使用长效溴隐亭还可克服许多患者在开始口服溴隐亭治疗后不久出现的依从性问题。