Sohár Gábor, Györkös Andrea, Dóczi Tamás, Kajtár Béla, Piski Zalán, Kovács Mónika
I. Belgyógyászati és Infektológiai Osztály,Zala Megyei Szent Rafael KórházZalaegerszeg, Zrínyi M. út 1., 8900.
Általános Orvostudományi Kar, Klinikai Központ, Idegsebészeti Klinika,Pécsi TudományegyetemPécs.
Orv Hetil. 2020 Mar;161(12):474-478. doi: 10.1556/650.2020.31697.
Thyrotropin-secreting pituitary tumors are rare causes of hyperthyroidism and account for less than 1% of all pituitary adenomas. The number of reported cases increased over the last few years as a consequence of the routine use of ultrasensitive immunometric assays for measuring thyrotropin levels. In the clinical practice, thyrotropin secreting adenomas must be considered in case of inappropriately normal to elevated thyrotropin in the presence of elevated free serum thyroid hormone levels. The authors present the case history of a middle aged female patient, who suffered from hyperthyreodism caused by a thyrotropin-secreting pituitary macroadenoma. After transient thyreostatic treatment, radical neurosurgical removal of the tumor was performed. The pituitary surgery was effective in restoring the patient's euthyreodism. The postoperative pituitary function remained intact. During follow-up, the recurrence of the disease was not detected. In our case report, the difficulties in the differential diagnoses are also discussed. Orv Hetil. 2020; 161(12): 474-478.
促甲状腺素分泌型垂体瘤是甲状腺功能亢进症的罕见病因,占所有垂体腺瘤的比例不到1%。由于常规使用超敏免疫测定法来检测促甲状腺素水平,过去几年报告的病例数量有所增加。在临床实践中,当游离血清甲状腺激素水平升高而促甲状腺素水平正常或升高不适当的情况下,必须考虑促甲状腺素分泌腺瘤。作者介绍了一名中年女性患者的病史,该患者因促甲状腺素分泌型垂体大腺瘤而患有甲状腺功能亢进症。经过短暂的甲状腺功能抑制治疗后,对肿瘤进行了根治性神经外科切除。垂体手术有效地恢复了患者的甲状腺功能正常。术后垂体功能保持完好。在随访期间,未检测到疾病复发。在我们的病例报告中,还讨论了鉴别诊断中的困难。《匈牙利医学周报》。2020年;161(12):474 - 478。