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巨大泌乳素腺瘤:196 例成人病例的详细分析。

Giant prolactinomas, a detailed analysis of 196 adult cases.

机构信息

Department of Endocrinology, Diabetology & Metabolism, Faculty of Medicine, Antwerp University Hospital, Drie Eikenstraat 655, Edegem, B-2650, Belgium.

Department of Nephrology, Antwerp University Hospital, Edegem, B-2650, Belgium.

出版信息

Pituitary. 2023 Oct;26(5):529-537. doi: 10.1007/s11102-023-01337-0. Epub 2023 Aug 7.

Abstract

PURPOSE

Giant prolactinomas are a rare entity, representing approximately 5% of all prolactinomas. A systematic review of 196 adult cases was performed. A comparison of the clinical, biochemical and radiological characteristics, management and therapeutic outcomes in men versus women is made.

METHODS

A structured search was conducted using the term 'giant prolactinoma'. Following inclusion criteria were used: diameter ≥ 40 mm, prolactin levels > 1000 ng/ml and no concomitant GH/ ACTH secretion.

RESULTS

196 cases were included [age: 38 (28-50) years, F/M ratio: 1/3.6]. Median tumor diameter was 53 (43-69) mm. Pituitary deficiency was present in 91% of cases, with hypogonadotropic hypogonadism being the most frequent. Most common presenting symptoms were visual impairment (73%) and headache (50%) in men and amenorrhea (58%) in women. 82% of cases were treated with a dopamine agonist (DA) as first-line treatment which led to normoprolactinemia, tumor shrinkage and visual improvement in 51%, 88% and 85% of cases, respectively. Surgery was performed in 29% of cases and all showed tumor remnant and persistent hyperprolactinemia. Women had a lower prolactin level and a smaller tumor diameter at diagnosis but pituitary deficiencies were more frequent and outcome was worse.

CONCLUSION

Giant prolactinomas are rare and have a male predominance. Visual impairment is the most frequent presenting symptom in men and amenorrhea in women. The gender-related difference in tumor size and level of prolactin was confirmed in this analysis where men had a larger diameter and a higher baseline prolactin level. DAs are the treatment of choice, irrespective of tumor size and presence of visual impairment. As only half of the cases achieved normoprolactinemia we do not, in contrast to previous literature, state giant prolactinomas to be exquisitely sensitive to DAs. Patient characteristics associated with persistent hyperprolactinemia after treatment with a DA were female gender, higher baseline prolactin and larger tumor size . This analysis did show TSH- and ACTH-deficiency to be more frequent after surgery which was not seen for LH/FSH deficiency.

摘要

目的

巨大泌乳素瘤是一种罕见的实体瘤,约占所有泌乳素瘤的 5%。对 196 例成年病例进行了系统回顾。对男性和女性的临床、生化和影像学特征、治疗方法和治疗结果进行了比较。

方法

使用术语“巨大泌乳素瘤”进行了结构化搜索。使用的纳入标准为:直径≥40mm,泌乳素水平>1000ng/ml,无同时分泌 GH/ACTH。

结果

纳入 196 例病例[年龄:38(28-50)岁,男女比例:1/3.6]。肿瘤直径中位数为 53(43-69)mm。91%的病例存在垂体功能减退,其中促性腺激素释放激素缺乏性性腺功能减退最常见。最常见的首发症状是男性的视力障碍(73%)和头痛(50%),女性的闭经(58%)。82%的病例采用多巴胺激动剂(DA)作为一线治疗,导致 51%、88%和 85%的病例泌乳素正常、肿瘤缩小和视力改善。29%的病例进行了手术,所有病例均有肿瘤残余和持续性高泌乳素血症。女性在诊断时的泌乳素水平和肿瘤直径较小,但垂体功能减退更常见,且结局更差。

结论

巨大泌乳素瘤罕见,男性多见。男性最常见的首发症状是视力障碍,女性是闭经。在这项分析中,男性的肿瘤直径和泌乳素基础水平较大,证实了性别相关的肿瘤大小和泌乳素水平差异。无论肿瘤大小和是否存在视力损害,DA 都是治疗的首选。由于只有一半的病例达到泌乳素正常,我们与以前的文献不同,并不认为巨大泌乳素瘤对 DA 极其敏感。DA 治疗后持续高泌乳素血症与患者特征相关,包括女性性别、较高的基础泌乳素和较大的肿瘤大小。该分析确实表明,与 LH/FSH 缺乏相比,手术后 TSH 和 ACTH 缺乏更为常见。

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