原发性色素沉着性结节性肾上腺皮质病所致的家族性库欣综合征。50年后的再次研究。 - Suppr

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超能文献

Familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease. Reinvestigation 50 years later.

作者信息

Young W F, Carney J A, Musa B U, Wulffraat N M, Lens J W, Drexhage H A

机构信息

Division of Endocrinology, Metabolism, and Internal Medicine, Mayo Clinic, Rochester, Minn 55905.

出版信息

N Engl J Med. 1989 Dec 14;321(24):1659-64. doi: 10.1056/NEJM198912143212407.

DOI:10.1056/NEJM198912143212407

PMID:2586567

Abstract

摘要

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Familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease. Reinvestigation 50 years later.原发性色素沉着性结节性肾上腺皮质病所致的家族性库欣综合征。50年后的再次研究。

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Carney complex, a familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease: a case report.卡尼综合征，一种由原发性色素沉着性结节性肾上腺皮质疾病引起的家族性库欣综合征：病例报告。

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Bilateral adrenal Cushing's syndrome: macronodular adrenal hyperplasia and primary pigmented nodular adrenocortical disease.双侧肾上腺库欣综合征：大结节性肾上腺增生和原发性色素性结节性肾上腺皮质疾病。

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[Combination of heart myxoma with primary nodular adrenal cortex dysplasia, spot-shaped skin pigmentation and myxoma-like tumors in other locations--a rare familial symptom complex ("Swiss syndrome")].

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Adrenocorticotropic hormone-independent Cushing's syndrome.促肾上腺皮质激素非依赖性库欣综合征

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Familial Cushing's syndrome due to nodular adrenocortical dysplasia is an inherited disease of immunological origin.

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