Neuroendocrine Unit, Department of Medicine, Massachusetts General Hospital, Zero Emerson Place # 112, Boston, MA 02114, USA.
Pituitary. 2013 Sep;16(3):287-93. doi: 10.1007/s11102-012-0419-3.
Patients with thyrotropin-secreting pituitary adenomas may present with mass effect, hypopituitarism, and/or hyperthyroidism. The spectrum of pathologic and clinical features of patients whose tumors demonstrate β-thyrotropin immunoreactivity (β-TSH IR) has not been characterized. To characterize the phenotype of patients with pituitary adenomas with positive β-TSH IR, we conducted a retrospective analysis of patient records of all adult patients (n = 1,223) undergoing pituitary surgery in our institution over one decade (1999-2009). The search identified 166 adults with tumors which had β-TSH IR. These patients were individually matched to 166 patients whose tumors revealed no β-TSH IR. Clinical, pathological, imaging and biochemical data were extracted. 332 patients, aged 51.4 ± 15.1 years [150 women (45 %) and 182 men (55 %)], with pituitary adenomas (mean tumor diameter ± SD: 22.7 ± 9.0 mm) were studied. The degree of β-TSH IR was associated with the presence of central hyperthyroidism (p < 0.0001) or goiter (p = 0.0217). Patients whose tumors expressed more extensive β-TSH IR were less likely to develop pituitary apoplexy than those without β-TSH IR (p = 0.0428). In addition, the degree of β-TSH IR correlated with the presence of immunoreactivity for β-FSH (p < 0.0001), β-LH (p < 0.0001), alpha subunit (p < 0.0001), and GH (p = 0.0036).
Pituitary adenomas expressing β-TSH IR were more likely to demonstrate immunoreactivity for β-FSH, β-LH, GH or alpha subunit. Patients with such tumors were more likely to exhibit hyperthyroidism and goiter, but less likely to develop pituitary apoplexy than patients without β-TSH IR. These findings suggest that β-TSH IR is associated with specific phenotypic features in patients with pituitary adenomas.
促甲状腺素分泌性垂体腺瘤患者可能出现肿块效应、垂体功能减退和/或甲状腺功能亢进。具有β-促甲状腺素免疫反应性(β-TSH IR)的肿瘤患者的病理和临床特征谱尚未确定。为了描述具有β-TSH IR 的垂体腺瘤患者的表型,我们对我院 10 年内(1999-2009 年)接受垂体手术的所有成年患者(n=1223)的患者记录进行了回顾性分析。检索确定了 166 名患有具有β-TSH IR 的肿瘤的成年人。这些患者与 166 名肿瘤未显示β-TSH IR 的患者进行了个体匹配。提取了临床、病理、影像学和生化数据。研究了 332 名年龄为 51.4±15.1 岁[150 名女性(45%)和 182 名男性(55%)]的患有垂体腺瘤(平均肿瘤直径±SD:22.7±9.0mm)的患者。β-TSH IR 的程度与中枢性甲状腺功能亢进(p<0.0001)或甲状腺肿(p=0.0217)的存在相关。与无β-TSH IR 的患者相比,肿瘤表达更广泛β-TSH IR 的患者更不可能发生垂体卒中(p=0.0428)。此外,β-TSH IR 的程度与β-FSH(p<0.0001)、β-LH(p<0.0001)、α亚单位(p<0.0001)和 GH(p=0.0036)的免疫反应性存在相关。
表达β-TSH IR 的垂体腺瘤更有可能表现出β-FSH、β-LH、GH 或α亚单位的免疫反应性。与无β-TSH IR 的患者相比,具有此类肿瘤的患者更有可能出现甲状腺功能亢进和甲状腺肿,但发生垂体卒中的可能性较小。这些发现表明,β-TSH IR 与垂体腺瘤患者的特定表型特征相关。