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一名患有先天性17α-羟化酶缺乏症女性的肾上腺髓质脂肪瘤。

Adrenal myelolipoma in a woman with congenital 17-hydroxylase deficiency.

作者信息

Condom E, Villabona C M, Gómez J M, Carrera M

出版信息

Arch Pathol Lab Med. 1985 Dec;109(12):1116-7.

PMID:3878142
Abstract

A case of adrenal myelolipoma, which to our knowledge is the first case to be associated with 17-hydroxylase deficiency, is reported. This rare, benign lesion is known to occur in association with other endocrinopathies. Discussion focuses on the possible role of continued stimulation by corticotropin and/or steroids as pathogenic factors. The present case adds evidence supporting this view.

摘要

据我们所知,本文报告了一例肾上腺髓质脂肪瘤,该病例为第一例与17-羟化酶缺乏相关的病例。这种罕见的良性病变已知与其他内分泌疾病有关。讨论聚焦于促肾上腺皮质激素和/或类固醇持续刺激作为致病因素的可能作用。本病例为支持这一观点增添了证据。

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