Growth hormone-, alpha-subunit and thyrotrophin-cosecreting pituitary adenoma in familial setting of pituitary tumour.

T P Links, J F Monkelbaan, R P Dullaart, T W van Haeften
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引用次数: 14

Abstract

A patient with acromegaly and hyperthyroidism due to a growth hormone-, thyrotrophin- and alpha-subunit-secreting pituitary adenoma is described. His decreased father had suffered from a pituitary tumour, and was likely to have had acromegaly as well. Plasma growth hormone and insulin-like growth factor I concentrations were elevated, with levels between 10 and 20 micrograms/l and 4.4 and 7.3 kU/l, respectively. In spite of hyperthyroidism (free thyroxine, 45 pmol/l; free triiodothyronine, 24 pmol/l), plasma thyrotrophin remained at 2.8 mU/l without any response to thyrotrophin-releasing hormone and could not be suppressed with exogenous administration of triiodothyronine. Plasma alpha-subunits were raised to 3.3-3.7 U/l (normal 0.4-1.1 U/l). Pathological examination of the surgically removed tumour showed a pituitary adenoma with the immunohistochemical presence of growth hormone, thyrotrophin, prolactin and alpha-subunit. This is the first report of a growth hormone-, thyrotrophin- and alpha-subunit-producing pituitary adenoma, which occurred in a familial setting.

垂体瘤家族性背景下的生长激素、α亚基和促甲状腺激素共分泌垂体腺瘤。
患者肢端肥大症和甲状腺机能亢进由于生长激素,促甲状腺素和α -亚单位分泌垂体腺瘤被描述。他日渐衰弱的父亲患有脑垂体瘤,很可能也患有肢端肥大症。血浆生长激素和胰岛素样生长因子I浓度升高,分别在10 ~ 20微克/升和4.4 ~ 7.3微克/升之间。尽管甲状腺机能亢进(游离甲状腺素,45 pmol/l;游离三碘甲状腺原氨酸,24 pmol/l),血浆促甲状腺素维持在2.8 mU/l,对促甲状腺素释放激素无反应,外源性三碘甲状腺原氨酸不能抑制。血浆α亚单位升高至3.3 ~ 3.7 U/l(正常为0.4 ~ 1.1 U/l)。手术切除肿瘤的病理检查显示垂体腺瘤,免疫组织化学存在生长激素,促甲状腺素,催乳素和α -亚基。这是第一个报告的生长激素,促甲状腺素和α -亚单位产生垂体腺瘤,这发生在一个家族设置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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