Division of Endocrinology and Metabolism, University of Toronto Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Endocr Pract. 2012 Sep-Oct;18(5):e121-6. doi: 10.4158/EP12033.CR.
To describe the case of a patient with an unusual plurihormonal pituitary adenoma with immunoreactivity for thyroid-stimulating hormone (TSH), growth hormone, follicle-stimulating hormone, prolactin, and α-subunit.
We report the clinical, laboratory, imaging, and pathology findings of a patient symptomatic from a plurihormonal pituitary adenoma and describe her outcome after surgical treatment.
A 60-year-old woman presented to the emergency department with headaches, blurry vision, fatigue, palpitations, sweaty hands, and weight loss. Her medical history was notable for hyperthyroidism, treated intermittently with methimazole. Magnetic resonance imaging disclosed a pituitary macroadenoma (2.3 by 2.2 by 2.0 cm), and preoperative blood studies revealed elevated levels of TSH at 6.11 mIU/L, free thyroxine at 3.6 ng/dL, and free triiodothyronine at 6.0 pg/mL. She underwent an uncomplicated transsphenoidal resection of the pituitary adenoma. Immunostaining of tumor tissue demonstrated positivity for not only TSH but also growth hormone, follicle-stimulating hormone, prolactin, and α-subunit. The Ki-67 index of the tumor was estimated at 2% to 5%, and DNA repair enzyme O6-methylguanine-DNA methyltransferase immunostaining was mostly negative. Electron microscopy showed the ultrastructural phenotype of a glycoprotein-producing adenoma. Postoperatively, her symptoms and hyperthyroidism resolved.
Thyrotropin-secreting pituitary adenomas are rare. Furthermore, recent reports suggest that 31% to 36% of adenomas may show evidence of secretion of multiple pituitary hormones. This case emphasizes the importance of considering pituitary causes of thyrotoxicosis and summarizes the clinical and pathology findings in a patient with a plurihormonal pituitary adenoma.
描述一例罕见的多激素垂体腺瘤病例,该腺瘤对促甲状腺激素(TSH)、生长激素、卵泡刺激素、催乳素和α亚单位具有免疫反应性。
我们报告了一例多激素垂体腺瘤患者的临床、实验室、影像学和病理学发现,并描述了她在手术治疗后的结果。
一名 60 岁女性因头痛、视力模糊、疲劳、心悸、手汗和体重减轻而到急诊就诊。她的病史值得注意,曾间歇性地用甲巯咪唑治疗甲状腺功能亢进症。磁共振成像显示垂体大腺瘤(2.3×2.2×2.0 cm),术前血液检查显示 TSH 水平升高至 6.11 mIU/L、游离甲状腺素为 3.6ng/dL 和游离三碘甲状腺原氨酸为 6.0pg/mL。她接受了经蝶窦切除术治疗垂体腺瘤。肿瘤组织的免疫染色不仅显示 TSH 阳性,还显示生长激素、卵泡刺激素、催乳素和α亚单位阳性。肿瘤的 Ki-67 指数估计为 2%至 5%,DNA 修复酶 O6-甲基鸟嘌呤-DNA 甲基转移酶免疫染色大多为阴性。电子显微镜显示糖蛋白分泌性腺瘤的超微结构表型。术后,她的症状和甲状腺功能亢进症得到缓解。
促甲状腺素分泌性垂体腺瘤较为罕见。此外,最近的报告表明,31%至 36%的腺瘤可能显示出分泌多种垂体激素的证据。本病例强调了考虑甲状腺毒症的垂体病因的重要性,并总结了一名多激素垂体腺瘤患者的临床和病理学发现。