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艾迪生病与垂体增大

Addison's Disease and Pituitary Enlargement.

作者信息

Winters Stephen J, Vitaz Todd, Nowacki Michael R, Craddock Durrett C, Silverman Craig

机构信息

Division of Endocrinology, Metabolism and Diabetes (SJW), University of Louisville School of Medicine, Louisville, Kentucky; Department of Radiation Oncology (CS), University of Louisville School of Medicine, Louisville, Kentucky; Brain Tumor Center (TV), Norton Neuroscience Institute; and Departments of Pathology (MRN), Radiology (DCC), Norton Health Care, Louisville, Kentucky.

出版信息

Am J Med Sci. 2015 Jun;349(6):526-9. doi: 10.1097/MAJ.0000000000000305.

Abstract

A 60-year-old man with Addison's disease, primary hypothyroidism and type 2 diabetes mellitus who was treated with stable doses of hydrocortisone and fludrocortisone developed increasing skin pigmentation and a bitemporal hemianopia. The plasma ACTH level was 14,464 pg/mL, and an invasive pituitary macroadenoma with suprasellar extension was found on magnetic resonance imaging leading to transnasal-transsphenoidal adenomectomy. The tumor demonstrated features of an eosinophilic adenoma and stained uniformly for ACTH. Residual tumor was treated with stereotactic radiotherapy. This case and the 13 cases published previously indicate that primary adrenal failure may predispose to corticotroph hyperplasia, and in some patients to the development of an invasive corticotroph adenoma. The ACTH level should be measured, and a pituitary magnetic resonance imaging is indicated when skin pigmentation increases in a patient with primary adrenal failure who is receiving customary treatment with glucocorticoids and mineralocorticoids.

摘要

一名60岁男性,患有艾迪生病、原发性甲状腺功能减退症和2型糖尿病,正在接受稳定剂量的氢化可的松和氟氢可的松治疗,却出现了皮肤色素沉着加重和双颞侧偏盲。血浆促肾上腺皮质激素(ACTH)水平为14464 pg/mL,磁共振成像发现有鞍上扩展的侵袭性垂体大腺瘤,遂行经鼻-经蝶窦腺瘤切除术。肿瘤表现为嗜酸性腺瘤特征,ACTH染色均匀。残留肿瘤接受立体定向放射治疗。该病例及之前发表的13例病例表明,原发性肾上腺功能衰竭可能易患促肾上腺皮质激素细胞增生,在某些患者中还易发展为侵袭性促肾上腺皮质激素腺瘤。对于正在接受糖皮质激素和盐皮质激素常规治疗的原发性肾上腺功能衰竭患者,当皮肤色素沉着增加时,应检测ACTH水平,并进行垂体磁共振成像检查。

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