Chiarini V, Graziano E, Cremonini N, Frank G, Zampa G A
Neurochirurgia (Stuttg). 1987 Mar;30(2):61-3. doi: 10.1055/s-2008-1053658.
We report a 28-year-old male with persistent clinical and laboratory findings of hyperthyroidism associated with marked elevated serum levels of TSH and no response to TRH despite hemithyroidectomy and subsequent antithyroid drug therapy two years previous to admission to our hospital. Subsequent skull X-rays, CT scans and angiographic findings demonstrated the presence of a pituitary tumour. After operation and radiation therapy T3, T4 and TSH levels returned to normal values. Seven years later the patient is still euthyroid. We conclude that hyperthyroidism in our patient was due to excessive secretion of TSH by the pituitary tumour.
我们报告一例28岁男性患者,尽管在入院前两年已行甲状腺次全切除术及随后的抗甲状腺药物治疗,但仍有持续的甲状腺功能亢进的临床和实验室检查结果,伴有血清促甲状腺激素(TSH)水平显著升高,且对促甲状腺激素释放激素(TRH)无反应。随后的头颅X线、CT扫描及血管造影检查结果显示存在垂体肿瘤。手术及放疗后,T3、T4及TSH水平恢复至正常范围。七年后,该患者甲状腺功能仍正常。我们得出结论,该患者的甲状腺功能亢进是由于垂体肿瘤分泌过多TSH所致。