Cooper D S, Wenig B M
Division of Endocrinology, Sinai Hospital of Baltimore, Maryland 21215, USA.
Thyroid. 1996 Aug;6(4):337-43. doi: 10.1089/thy.1996.6.337.
A woman developed what appeared to be typical Graves' disease in 1965 at the age of 45 years. After 9 years of antithyroid drug therapy, she was treated with radioiodine. Ten years later (1985) she developed postablative hypothyroidism. Despite replacement doses of thyroxine that resulted in thyroid hormone levels that were in the hyperthyroid range, TSH levels remained elevated. Initial biochemical studies, including a high alpha-subunit to TSH ratio, suggested a pituitary TSH-secreting tumor, but a CT scan of the sella turcica was normal. In 1994, while undergoing an otolaryngologic examination, the patient was found to have a nasopharyngeal mass lesion, which was ultimately shown histologically and immunohistochemically to be an ectopic pituitary tumor. Resection of the mass restored TSH and alpha-subunit levels to normal. This patient probably represents the first ectopic TSH-secreting pituitary tumor to be reported.
一名女性在1965年45岁时患上了看似典型的格雷夫斯病。经过9年的抗甲状腺药物治疗后,她接受了放射性碘治疗。10年后(1985年),她出现了放射性碘治疗后甲状腺功能减退。尽管给予了替代剂量的甲状腺素,使甲状腺激素水平处于甲状腺功能亢进范围,但促甲状腺激素(TSH)水平仍升高。最初的生化研究,包括高α亚基与TSH比值,提示存在垂体分泌TSH的肿瘤,但蝶鞍的计算机断层扫描(CT)正常。1994年,该患者在接受耳鼻喉科检查时,发现有鼻咽部肿块病变,最终经组织学和免疫组织化学检查证实为异位垂体肿瘤。切除肿块后,TSH和α亚基水平恢复正常。该患者可能是首例报道的异位分泌TSH的垂体肿瘤。