Service d'Endocrinologie, Centre Hospitalier Universitaire de Mont-Godinne, Université Catholique de Louvain, B-5530 Mont-sur-Meuse, Belgium.
Eur J Endocrinol. 2013 Nov 22;170(1):31-8. doi: 10.1530/EJE-13-0503. Print 2014 Jan.
To characterise distinctive clinical features of giant prolactinomas in women.
A multicentre, retrospective case series and literature review.
We collected data from 15 female patients with a pituitary tumour larger than 4 cm and prolactin levels above 1000 μg/l and identified 19 similar cases from the literature; a gender-based comparison of the frequency and age distribution was obtained from a literature review.
The initial PubMed search using the term 'giant prolactinomas' identified 125 patients (13 women) responding to the inclusion criteria. The female:male ratio was 1:9. Another six female patients were found by extending the literature search, while our own series added 15 patients. The median age at diagnosis was 44 years in women compared with 35 years in men (P<0.05). All cases diagnosed before the age of 15 years were boys. In women (n=34), we observed a minor peak incidence during the third decade of life and a major peak during the fifth decade. Amenorrhoea was a constant feature with seven cases of primary amenorrhoea. In eight women with onset of secondary amenorrhoea before the age of 40 years, the diagnosis was made 2-31 years later (median 9 years) and in all but one because of tumour pressure symptoms. The prolactin levels were above 10,000 μg/l in 15/34 and misdiagnosis due to 'hook effect' occurred in two of them. Eighteen patients were treated with cabergoline; standard doses (<2.0 mg/week) were able to normalise prolactin in only 4/18 patients, and 7/18 patients were resistant to weekly doses ranging from 3.0 to 7.0 mg.
Giant prolactinomas are rare in women, often resistant to dopamine agonists and seem to be distributed in two age groups, with a larger late-onset peak.
描述女性巨大泌乳素瘤的独特临床特征。
一项多中心、回顾性病例系列研究和文献回顾。
我们从 15 名垂体瘤大于 4 厘米且泌乳素水平高于 1000μg/l 的女性患者中收集数据,并从文献中确定了 19 例相似病例;从文献回顾中获得了基于性别的频率和年龄分布比较。
最初使用术语“巨大泌乳素瘤”在 PubMed 上进行的搜索确定了符合纳入标准的 125 名患者(13 名女性)。女性与男性的比例为 1:9。通过扩展文献搜索发现了另外 6 名女性患者,而我们自己的系列增加了 15 名患者。女性患者的中位诊断年龄为 44 岁,而男性为 35 岁(P<0.05)。所有在 15 岁之前诊断的病例均为男孩。在女性(n=34)中,我们观察到第三个十年有一个较小的发病高峰,第五个十年有一个较大的发病高峰。闭经是一个常见特征,有 7 例原发性闭经。在 8 名 40 岁前发生继发性闭经的女性中,诊断时间为 2-31 年后(中位时间为 9 年),且除 1 例外均因肿瘤压迫症状而诊断。34 例患者中,有 15 例泌乳素水平高于 10,000μg/l,其中 2 例因“钩状效应”导致误诊。18 例患者接受卡麦角林治疗;标准剂量(<2.0mg/周)仅能使 4/18 例患者的泌乳素恢复正常,7/18 例患者对每周 3.0-7.0mg 的剂量均有耐药性。
女性巨大泌乳素瘤罕见,常对多巴胺激动剂耐药,似乎分布在两个年龄组,有一个较大的迟发性发病高峰。