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[A case of deoxycorticosterone-producing adrenal tumor].

作者信息

Komura T, Uekado Y, Suzuki A, Miyai M

机构信息

Department of Urology, Wakayama Medical College.

出版信息

Hinyokika Kiyo. 1993 Feb;39(2):145-9.

PMID:8465688
Abstract

We present a case of a 11-deoxycorticosterone (DOC)-producing adrenocortical tumor. A 55-year-old female was admitted to our hospital with the chief complaints of sustained hypertension and weakness of lower extremities. A laboratory study revealed a decrease in the serum potassium level and plasma renin activity, a normal level of plasma aldosterone and a significant elevation of plasma DOC and 18-OH-DOC levels. The plasma DOC level was increased by ACTH stimulation and was not suppressed by dexamethasone. The tumor appeared at a low intensity of the T1 weighted image of magnetic resonance imaging (MRI) and at a high intensity on the T2 weighted image. Left adrenalectomy was performed and histological examination revealed a benign adrenal adenoma. Postoperatively, the abnormal blood pressure, serum potassium level and plasma level of DOC and 18-OH-DOC became normal.

摘要

相似文献

1
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Hinyokika Kiyo. 1993 Feb;39(2):145-9.
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Response of several adrenal steroids to ACTH stimulation in essential hypertension.原发性高血压患者几种肾上腺类固醇对促肾上腺皮质激素刺激的反应。
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Intern Med. 1996 Feb;35(2):123-8. doi: 10.2169/internalmedicine.35.123.
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引用本文的文献

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11-Deoxycorticosterone Producing Adrenal Hyperplasia as a Very Unusual Cause of Endocrine Hypertension: Case Report and Systematic Review of the Literature.11-脱氧皮质酮产生的肾上腺增生症作为一种非常罕见的内分泌性高血压病因:病例报告及文献系统回顾。
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