首页> 外文期刊>Endocrine journal >Adrenal Insufficiency after Incomplete Resection of Pituitary Macrocorticotropinoma of Cushing's Disease: Role of High Molecular Weight ACTH
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Adrenal Insufficiency after Incomplete Resection of Pituitary Macrocorticotropinoma of Cushing's Disease: Role of High Molecular Weight ACTH

机译:库欣病的垂体大促肾上腺皮质激素瘤不完全切除后的肾上腺功能不全:高分子量ACTH的作用

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摘要

A 15-year-old girl with Cushing's disease exhibited adrenal insufficiency following incomplete trans- sphenoidal resection of a large pituitary corticotropinoma, approximately 35 mm in diameter. Within two weeks following surgery, her plasma ACTH level decreased from 42 to 13 pmol/l, while, her plasma cortisol levels and urinary excretion of free cortisol decreased from 607 nmol/l and 1112 nmol/day to 94 nmol/l and 55 nmol/day, respectively. Immunoreactive ACTH was characterized in plasma using Sephadex Go75 column chromatography and measuring ACTH with immunoradiometric assay (IRMA) and radioimmunoassay (RIA) to determine additional peaks, other than the one demonstrated for 1-39 ACTH.
机译:一名患有库欣病的15岁女孩在经大直径脑垂体肾上腺皮质激素瘤的经蝶窦切除术不完全后表现出肾上腺功能不全。手术后两周内,血浆ACTH水平从42 pmol / l降至13 pmol / l,而血浆皮质醇水平和游离皮质醇的尿排泄从607 nmol / l和1112 nmol / day降至94 nmol / l和55 nmol /天。使用Sephadex Go75柱色谱法在血浆中表征免疫反应性ACTH,并用免疫放射测定法(IRMA)和放射免疫测定法(RIA)测量ACTH以确定其他峰,但1-39 ACTH所证实的峰除外。

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