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垂体结石:两例分泌促甲状腺素的垂体腺瘤致密钙化病例

Pituitary stone: two cases of densely calcified thyrotrophin-secreting pituitary adenomas.

作者信息

Webster J, Peters J R, John R, Smith J, Chan V, Hall R, Scanlon M F

机构信息

Department of Medicine, University of Wales College of Medicine, Heath Park, Cardiff, UK.

出版信息

Clin Endocrinol (Oxf). 1994 Jan;40(1):137-43. doi: 10.1111/j.1365-2265.1994.tb02456.x.

Abstract

Calcification is a well recognized but relatively uncommon feature of prolactin-secreting, growth hormone-secreting and non-functional pituitary tumours. It varies in extent, but rarely exceeds a tiny amount histologically or radiologically. Thyrotroph adenomas are the rarest of the secretory pituitary tumours, accounting for less than 1% of cases, and partial calcification of such lesions has been reported in only three cases. We describe two patients in whom the clinical and biochemical features indicated the presence of a TSH-secreting adenoma and radiology demonstrated a large 'pituitary stone'. One patient, a 59-year-old female, initially presented with hyperthyroidism, aged 18, and was rendered euthyroid by two subtotal thyroidectomies before a pituitary lesion was suspected, over 20 years later. Autonomous secretion of thyrotrophin was demonstrated by dynamic tests, and the failure of exogenous T3 to reduce the serum TSH. In the absence of tumour expansion and compressive symptoms, pituitary surgery was not undertaken. At the age of 56, she developed symptoms of intermittent ataxia and diplopia, culminating in a focal seizure, and was found on CT scan to have, in addition to the pituitary lesion, a parasagittal meningioma. This was successfully removed at craniotomy. In the second patient, a 42-year-old male, the finding of hyperthyroidism in association with an elevated TSH concentration led to the discovery of a pituitary stone which was removed transethmoidally, together with surrounding adenomatous tissue which stained positively for TSH on immunocytochemistry.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

钙化是一种已被充分认识但相对不常见的泌乳素分泌型、生长激素分泌型和无功能垂体瘤的特征。其程度各异,但在组织学或放射学上很少超过微量。促甲状腺素细胞腺瘤是分泌型垂体瘤中最罕见的,占病例不到1%,仅3例报告过此类病变的部分钙化情况。我们描述了两名患者,其临床和生化特征提示存在促甲状腺素分泌腺瘤,放射学检查显示有巨大的“垂体结石”。一名59岁女性患者,18岁时最初表现为甲状腺功能亢进,在怀疑有垂体病变的20多年前,经两次甲状腺次全切除术后甲状腺功能恢复正常。动态试验证实促甲状腺素自主分泌,外源性T3未能降低血清促甲状腺素。由于无肿瘤扩大和压迫症状,未进行垂体手术。56岁时,她出现间歇性共济失调和复视症状,最终发生局灶性癫痫发作,CT扫描发现除垂体病变外,还有矢状窦旁脑膜瘤。开颅手术成功切除了该脑膜瘤。第二名患者是一名42岁男性,因甲状腺功能亢进伴促甲状腺素浓度升高而发现垂体结石,经筛窦入路切除了垂体结石及周围免疫细胞化学染色促甲状腺素呈阳性的腺瘤组织。(摘要截短于250字)

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