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儿童和青少年高泌乳素血症与泌乳素瘤病例的长期随访结果:单中心经验。

Hyperprolactinemia in children and adolescents and longterm follow-up results of prolactinoma cases: a single-centre experience.

机构信息

Department of Pediatric Endocrinology, Ankara University Faculty of Medicine, Ankara, Türkiye.

出版信息

Turk J Pediatr. 2022;64(5):892-899. doi: 10.24953/turkjped.2021.4639.

Abstract

BACKGROUND

Hyperprolactinaemia refers to increased circulating prolactin and is divided into functional and pathological hyperprolactinaemia. Prolactinoma is the most common cause of severe hyperprolactinaemia. Prolactinomas are rare in children. Treatment outcomes and long-term follow-up data in children are insufficient. Dopamine agonists are the first step in the treatment of prolactinomas. There are no recommendations supported by a high level of evidence regarding the dose and duration of cabergoline treatment.

METHODS

Patients with hyperprolactinaemia were evaluated for etiological, clinical, and follow-up characteristics. The case files of patients with high prolactin levels who were followed up in our clinic between 2001 and 2019 were reviewed retrospectively.

RESULTS

27 cases (20 female, 7 male) with hyperprolactinemia were detected. The median age of the cases was 15 years (0.3-17.4). Prolactinoma was detected in 40.7% of the cases (n=11). Among these cases, six were macroadenomas. The median prolactin level was 118 ng/mL (34-4340) in those with prolactinoma and 60 ng/mL (22-200) in the hyperprolactinaemia group (p=0.007). In the prolactinoma group, the median age at presentation in macroadenoma cases (13.8 years) was lower than in microadenoma cases (17 years) (p=0.06). There was a negative correlation between prolactin level and height SDS (r=-0.770, p=0.06). In all cases, the median initial cabergoline dose was 0.5 mg/week, and prolactin levels returned to normal within an average of 2.6±2.4 months. Cabergoline treatment achieved a 50% reduction in adenoma size in the first year of treatment without high doses.

CONCLUSIONS

Prolactinoma consists of an important group among hyperplolactinemia in children. In our study, prolactinoma was detected in 40.7% of children with hyperplolactinemia, and children with prolonged use (over 4 years) tolerated cabergoline well and prolactin levels normalized without high doses. Follow-up is required for relapse after discontinuing the treatment.

摘要

背景

高催乳素血症是指循环催乳素升高,分为功能性和病理性高催乳素血症。催乳素瘤是引起严重高催乳素血症的最常见原因。催乳素瘤在儿童中很少见。儿童的治疗结果和长期随访数据不足。多巴胺激动剂是治疗催乳素瘤的第一步。卡麦角林治疗的剂量和持续时间没有得到高水平证据支持的建议。

方法

对高催乳素血症患者的病因、临床和随访特征进行评估。回顾性分析了 2001 年至 2019 年在我院接受随访的高催乳素血症患者的病例资料。

结果

共检测到 27 例(20 例女性,7 例男性)高催乳素血症患者。病例的中位年龄为 15 岁(0.3-17.4)。催乳素瘤占 40.7%(n=11)。这些病例中有 6 例为大腺瘤。催乳素瘤患者的催乳素水平中位数为 118ng/ml(34-4340),高催乳素血症组为 60ng/ml(22-200)(p=0.007)。催乳素瘤组中,大腺瘤病例的发病年龄(13.8 岁)低于微腺瘤病例(17 岁)(p=0.06)。催乳素水平与身高 SDS 呈负相关(r=-0.770,p=0.06)。所有患者的初始卡麦角林剂量中位数为 0.5mg/周,平均 2.6±2.4 个月后催乳素水平恢复正常。卡麦角林治疗在第一年可使腺瘤体积缩小 50%,无需高剂量。

结论

催乳素瘤是儿童高催乳素血症的重要组成部分。在我们的研究中,儿童高催乳素血症中催乳素瘤的检出率为 40.7%,儿童长期(超过 4 年)使用卡麦角林耐受良好,且在无需高剂量的情况下催乳素水平正常化。治疗停止后需要随访以防止复发。

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