Thyrotrophs in PIT1-lineage Pituitary Neuroendocrine Tumours Without Syndrome of Inappropriate Secretion of Thyrotropin Stimulating Hormone

IF 2.4 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Eri Kasuga, Naoko Inoshita, Noriaki Tanabe, Atsushi Ishida, Masataka Kato, Haruko Yoshimoto, Hideki Shiramizu, Go Matsuoka, Koji Takano, Shozo Yamada, Rimei Nishimura
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Abstract

Objective

Many patients with pituitary neuroendocrine tumours (PitNETs) containing beta (β) thyroid-stimulating hormone (TSH)-immunopositive cells, without syndrome of inappropriate secretion of TSH (SITSH), show a significant reduction in TSH levels following surgical removal of the tumour-like functioning thyrotroph PitNET. We evaluated the pathophysiological and clinical characteristics of TSH-positive cells in PIT1-lineage PitNETs in patients without the syndrome of inappropriate secretion of TSH.

Design

Retrospective cohort study.

Patients and Mesurements

Overall, 165 patients diagnosed with PIT1-lineage PitNETs without SITSH between April 2018 and July 2023 at Moriyama Memorial Hospital were reviewed. They were categorised into three groups based on the rate of βTSH-immuno-positive cells in their PitNETs: strongly positive group with 10% or more βTSH-immuno-positive cells, weakly positive group with less than 10%, and negative group. Clinical data from these groups were compared.

Results

Patient age, sex, and tumour size did not differ significantly among the groups. Most of the weakly positive cases had acromegaly, whereas many of the strongly positive cases had clinically nonfunctioning tumours. Preoperative TSH levels were slightly higher in strongly positive cases than in the other groups but fell within the normal range postoperatively, whereas postoperative TSH levels were significantly lower across all groups. The degree of TSH reduction postoperatively was significantly higher in the strongly positive group.

Conclusions

In the strongly positive group, TSH levels decreased significantly after surgery, whereas no such decrease was observed in the other two groups, suggesting that thyrotrophs in strongly positive PitNETs are TSH-producing, similar to clinically functioning thyrotroph PitNETs.

无促甲状腺激素分泌异常综合征的pit1系垂体神经内分泌肿瘤中的促甲状腺激素。
目的:许多垂体神经内分泌肿瘤(PitNETs)患者含有β (β)促甲状腺激素(TSH)免疫阳性细胞,没有TSH不适当分泌综合征(SITSH),在手术切除肿瘤样功能甲状腺激素PitNET后,TSH水平显著降低。我们评估了没有TSH不适当分泌综合征的患者中pit1谱系PitNETs中TSH阳性细胞的病理生理和临床特征。设计:回顾性队列研究。患者和测量:总体而言,2018年4月至2023年7月在森山纪念医院诊断为pit1谱系PitNETs的165例患者无SITSH。根据其PitNETs中β tsh免疫阳性细胞的比例将其分为三组:β tsh免疫阳性细胞10%或以上的强阳性组,小于10%的弱阳性组和阴性组。比较两组的临床资料。结果:患者年龄、性别和肿瘤大小在组间无显著差异。大多数弱阳性病例有肢端肥大症,而许多强阳性病例有临床无功能肿瘤。强阳性病例术前TSH水平略高于其他组,但术后TSH水平均在正常范围内,而所有组术后TSH水平均显著低于其他组。强阳性组术后TSH降低程度明显高于对照组。结论:在强阳性组中,手术后TSH水平显著下降,而在其他两组中没有观察到这种下降,这表明强阳性PitNETs中的促甲状腺激素产生TSH,类似于临床功能的促甲状腺PitNETs。
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来源期刊
Clinical Endocrinology
Clinical Endocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
3.10%
发文量
192
审稿时长
1 months
期刊介绍: Clinical Endocrinology publishes papers and reviews which focus on the clinical aspects of endocrinology, including the clinical application of molecular endocrinology. It does not publish papers relating directly to diabetes care and clinical management. It features reviews, original papers, commentaries, correspondence and Clinical Questions. Clinical Endocrinology is essential reading not only for those engaged in endocrinological research but also for those involved primarily in clinical practice.
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