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嗜铬细胞瘤与对侧无功能肾上腺皮质腺瘤的独特关联。

Unique association of pheochromocytoma with contralateral nonfunctioning adrenal cortical adenoma.

作者信息

Morimoto S, Sasaki S, Moriguchi J, Miki S, Kawa T, Nakamura K, Fujita H, Itoh H, Nakata T, Takeda K, Nakagawa M

机构信息

Second Department of Medicine, Kyoto Prefectural University of Medicine, Japan.

出版信息

Am J Hypertens. 1998 Jan;11(1 Pt 1):117-21. doi: 10.1016/s0895-7061(97)00369-5.

Abstract

A 57-year-old woman complaining of hypertensive attacks associated with headache and palpitation was admitted to our hospital for examination of bilateral adrenal tumors in 1985. After right pheochromocytoma was diagnosed, right adrenalectomy was performed. The left adrenal tumor was small; thus, the left adrenal tumor was preserved to avoid adrenal insufficiency, although left adrenal pheochromocytoma could not be denied. In 1995, she was referred to our clinic again because of recurrent headache and palpitation, and enlargement of the left adrenal tumor. Although pheochromocytoma was suspected again, the enlarged left adrenal turned out to be a nonfunctioning cortical adenoma. This case was interesting, not only because of difficulty in identifying the left adrenal tumor, but also because of the rare coexistence of a pheochromocytoma and a nonfunctioning adrenal cortical tumor.

摘要

一名57岁女性因伴有头痛和心悸的高血压发作前来就诊,于1985年入住我院以检查双侧肾上腺肿瘤。在诊断为右侧嗜铬细胞瘤后,实施了右侧肾上腺切除术。左侧肾上腺肿瘤较小;因此,尽管不能排除左侧肾上腺嗜铬细胞瘤,但为避免肾上腺功能不全,保留了左侧肾上腺肿瘤。1995年,她因复发性头痛和心悸以及左侧肾上腺肿瘤增大再次转诊至我院门诊。尽管再次怀疑为嗜铬细胞瘤,但增大的左侧肾上腺结果是一个无功能的皮质腺瘤。该病例很有意思,不仅因为难以识别左侧肾上腺肿瘤,还因为嗜铬细胞瘤与无功能肾上腺皮质肿瘤罕见共存。

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