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伴有原发性肾上腺皮质微腺瘤病(原发性肾上腺皮质结节性发育异常)的家族性库欣综合征

Familial Cushing's syndrome with primary adrenocortical microadenomatosis (primary adrenocortical nodular dysplasia).

作者信息

Schweizer-Cagianut M, Froesch E R, Hedinger C

出版信息

Acta Endocrinol (Copenh). 1980 Aug;94(4):529-35. doi: 10.1530/acta.0.0940529.

Abstract

Cushing's syndrome was found in 2 of 4 siblings all of which also had other malformations. After bilateral adrenalectomy no hyperpigmentation was noted. Morphologically the adrenals of both siblings with Cushing's syndrome showed the typical lesions of the so-called microadenomatosis or primary adrenocortical nodular dysplasia with foci of eosinophilic giant cells. This is a new form of Cushing's syndrome due to an inborn error of the adrenals and no hypothalamic-pituitary dysfunction.

摘要

在4名兄弟姐妹中有2人被发现患有库欣综合征,他们均还伴有其他畸形。双侧肾上腺切除术后未发现色素沉着。从形态学上看,两名患有库欣综合征的兄弟姐妹的肾上腺均显示出所谓的微腺瘤病或原发性肾上腺皮质结节性发育异常的典型病变,并伴有嗜酸性巨细胞灶。这是一种由肾上腺先天性缺陷引起的新型库欣综合征,不存在下丘脑 - 垂体功能障碍。

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