首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Surgical management of clinically silent thyrotropin pituitary adenomas: A single center series of 20 patients
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Surgical management of clinically silent thyrotropin pituitary adenomas: A single center series of 20 patients

机译:临床沉默甲状腺醇垂体腺瘤的手术管理:单中心系列20例患者

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Silent thyrotropin pituitary adenomas (TSHomas) are defined by absence of hyperthyroidism despite TSH immunopositivity. Data pertaining to clinical and surgical characteristics of silent TSHomas remains limited. We aim to describe the clinical presentation, pathological characteristics, and outcomes in silent TSHoma patients treated at a tertiary pituitary center. We retrospectively identified patients with histologically-proven silent TSHoma who underwent transsphenoidal resection at our center between 2000 and 2016 (n = 1244 total patients). Patients with preoperative hyperthyroidism or thyroidectomy were excluded. Twenty patients with silent TSHomas were included (1.6% of surgically treated PAs), of which 35% were reoperations. Presenting symptoms included vision loss (45%) and headache (40%). Preoperative pituitary dysfunction included hypothyroidism (40%), hypogonadotropic hypogonadism (30%), and panhypopituitarism (15%). Nineteen patients (95%) had macroadenomas (mean diameter 29.9 mm). Extrasellar growth was identified in 17 patients (85%) and 65% had cavernous sinus invasion. Immunostaining for alpha-subunit was positive in 19 patients (95%), and 75% of tumors expressed immunopositivity for hormones other than TSH. Gross total tumor resection was achieved in 9 patients (45%) on follow-up MRI. Major postoperative complications included hydrocephalus (1 patient) and cerebrospinal fluid leak with meningitis (1 patient). Tumor progression and recurrence occurred in 1 patient each (10% total) over the follow-up period (median 18.5 months). Silent TSHomas tend to be large, invasive tumors. In addition to TSH, a majority express immunopositivity for alpha-subunit and gonadotropins, thereby potentially supporting a primitive adenoma lineage and subtype. Despite reoperation in several patients, good overall outcomes with low complication rates were achieved. (C) 2019 Elsevier Ltd. All rights reserved.
机译:沉默的甲状腺激素垂体腺瘤(TShomas)通过缺乏甲状腺功能亢进而定义,尽管免疫阳性。与静音Tshomas的临床和外科特征有关的数据仍然有限。我们的目标是描述在初级垂体中心治疗的静音Tshoma患者中的临床介绍,病理特征和结果。我们回顾性地鉴定了在2000年至2016年至2016年期间在我们的中心接受过分离子切除术的组织学过的沉默Tshoma(N = 1244例)。术前甲状腺功能亢进或甲状腺切除术的患者被排除在外。包括二十个沉默TShomas患者(1.6%的手术治疗PAS),其中35%是重新进展。呈现症状包括视力丧失(45%)和头痛(40%)。术前垂体功能障碍包括甲状腺功能亢进(40%),低血糖增生性腺性腺低因素(30%)和胰腺炎术(15%)。 19名患者(95%)具有Macroadenomas(平均直径29.9 mm)。在17名患者(85%)和65%患者中鉴定了外壳生长,并且患有海绵窦入侵。 α-亚基的免疫染色于19名患者(95%),75%的肿瘤表达了TSH以外的激素的免疫阳性。在后续MRI上的9例患者(45%)中达到总肿瘤切除术。主要的术后并发症包括脑膜(1例患者)和脑脊液泄漏脑膜炎(1例患者)。肿瘤进展和复发发生在1例患者(总共10%)上发生在后续期间(中位数18.5个月)。沉默的Tshomas往往是大,侵入性的肿瘤。除了TSH之外,对于α-亚基和促性腺激素的大多数表达免疫阳性,从而潜在地支持原始腺瘤谱系和亚型。尽管在几名患者中重新进食,但实现了良好的并发率的整体结果。 (c)2019年elestvier有限公司保留所有权利。

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