Trukhina D A, Przhiyalkovskaya E G, Belaya Zh E, Grigoriev A Yu, Azizyan V N, Mamedova E O, Rozhinskaya L Ya, Lapshina A M, Pigarova E A, Dzeranova L K, Platonova N M, Troshina E A, Melnichenko G A
Endocrinology Research Centre.
Probl Endokrinol (Mosk). 2023 Sep 27;70(2):23-36. doi: 10.14341/probl13325.
Thyrotropin-secreting pituitary adenomas (TSH-PA) are a rare cause of thyrotoxicosis and account for 0.5-2% of all pituitary adenomas. Taking into account the rarity of the disease, it is extremely important to analyze each case of TSH-PA.
To analyze the clinical characteristics and treatment outcomes of patients with TSH-PA, as well as to determine preoperative and early postoperative factors that predict long-term remission.
In a single-center retrospective study we analyzed clinical signs, laboratory and instrumental studies, as well as the treatment outcomes of patients with TSH-PA from 2010 to 2023. Preoperative factors, as well as TSH level measured on day 3 postoperatively, were evaluated for their ability to predict long-term remission when comparing groups of patients with and without remission.
The study included 45 patients with TSH-PA (14 men, 31 women), with a median age of 45 years [30; 57]. The most common clinical manifestations of TSH-PA were: cardiac arrhythmia in 37 (82.2%) patients, thyroid pathology in 27 (60%), neurological disorders in 24 (53.35%). Most PAs were macroadenomas (n=35, 77.8%). Preoperatively, 28 (77.8%) patients received somatostatin analogs, and 20 (71.4%) patients were euthyroid at the time of surgery. Surgical treatment was performed in 36 (80%) patients, postoperative remission was achieved in 31 cases (86.1%). Administration of somatostatin analogues to patients with no remission/relapse after surgery lead to the remission in 100% of cases (4/4). A 1 mm increase in PA size raised the odds of recurrence/no remission by 1.15-fold,and PA invasion during surgery - by 5.129 fold. A TSH level on day 3 postoperatively above 0.391 mIU/L (AUC, 0.952; 95% CI 0.873-1.000; standard error 0.04; p<0.001) identifies patients with relapse/absence of remission after surgical treatment (sensitivity = 100%, specificity = 88.9%).
The TSH-PA in the structure of PAs is extremely rare, and as a result, most of them are misdiagnosed and detected already at the stage of macroadenoma. The most effective method of treatment is transnasal transsphenoidal adenomectomy. Somatostatin analogues can be used as second-line therapy if surgical treatment is ineffective. We have proposed a possible model for postoperative TSH levels (>0.391 mU/l) to predict recurrence of TSH-PA, which requires validation on an expanded number of cases.
促甲状腺素分泌型垂体腺瘤(TSH-PA)是甲状腺毒症的罕见病因,占所有垂体腺瘤的0.5%-2%。鉴于该疾病的罕见性,分析每一例TSH-PA病例极为重要。
分析TSH-PA患者的临床特征和治疗结果,以及确定预测长期缓解的术前和术后早期因素。
在一项单中心回顾性研究中,我们分析了2010年至2023年TSH-PA患者的临床体征、实验室和影像学检查结果以及治疗结果。在比较缓解和未缓解患者组时,评估术前因素以及术后第3天测得的TSH水平预测长期缓解的能力。
该研究纳入了45例TSH-PA患者(14例男性,31例女性),中位年龄为45岁[30;57]。TSH-PA最常见的临床表现为:37例(82.2%)患者出现心律失常,27例(60%)患者有甲状腺病变,24例(53.35%)患者有神经功能障碍。大多数垂体腺瘤为大腺瘤(n=35,77.8%)。术前,28例(77.8%)患者接受了生长抑素类似物治疗,20例(71.4%)患者在手术时甲状腺功能正常。36例(80%)患者接受了手术治疗,31例(86.1%)患者术后实现缓解。对术后未缓解/复发的患者给予生长抑素类似物治疗,100%的病例(4/4)实现缓解。垂体腺瘤大小每增加1mm,复发/未缓解的几率增加1.15倍,手术中垂体腺瘤侵袭则增加5.129倍。术后第3天TSH水平高于0.391 mIU/L(AUC,0.952;95%CI 0.873-1.000;标准误差0.04;p<0.001)可识别手术治疗后复发/未缓解的患者(敏感性=100%,特异性=88.9%)。
在垂体腺瘤结构中,TSH-PA极为罕见,因此大多数病例在大腺瘤阶段才被误诊和发现。最有效的治疗方法是经鼻蝶窦腺瘤切除术。如果手术治疗无效,生长抑素类似物可作为二线治疗药物。我们提出了一个术后TSH水平(>0.391 mU/l)预测TSH-PA复发的可能模型,这需要在更多病例中进行验证。