Graves病伴嗜铬细胞瘤1例报告

Jin Hwa Kim, Sang Jun Lee, J. Shin, M. You, Jae Sik Jung, Sang Yong Kim, H. Bae
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引用次数: 1

摘要

我们报告一例罕见的格雷夫斯病合并嗜铬细胞瘤,患者尿和血清中儿茶酚胺及其代谢物水平正常。一位45岁的女性因胸部计算机断层扫描发现的右肾上腺偶发瘤而被转介至我院。1个月前,她被诊断为格雷夫斯病。患者无高血压等嗜铬细胞瘤症状,也无高血压发作史。连续两个24小时的尿样被送到实验室测量儿茶酚胺,两个样本都显示正常水平的肾上腺素和香草扁桃酸(VMA)。右肾上腺切除术后,最终病理诊断为肾上腺嗜铬细胞瘤。本病例提示Graves病的发病可能与嗜铬细胞瘤分泌过量儿茶酚胺有关。此外,虽然检测嗜铬细胞瘤的常规方法是确定尿儿茶酚胺的增加,但医生应该意识到这种检测可能出现假阴性。(韩国博士
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Graves' Disease Accompanied by Pheochromocytoma: Report of a Case
We present here a rare case of Graves' disease accompanied by pheochromocytoma, and the patient showed normal urine and serum levels of catecholamines and their metabolites. A 45-year-old woman was referred to our hospital for the evaluation of a right adrenal incidentaloma that was detected by chest computed tomography. She had been diagnosed with Graves' disease 1 month previously. She had no symptoms of pheochromocytoma such as hypertension or a history of hypertension attack. Two consecutive 24-hour urine samples were sent to the lab for measurement of the catecholamines, and both samples showed normal levels of metanephrine and vanillylmandelic acid (VMA). After right adrenalectomy was performed, the final pathological diagnosis was adrenal pheochromocytoma. This case suggests that the onset of Graves' disease may be associated with excess catecholamine secreted by a pheochromocytoma. In addition, although the conventional method for detecting pheochromocytoma is to identify an increase of the urine catecholamines, physicians should be aware of the possibility of false negativity on this test. (J Korean Endocr Soc
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