PDF(Pubmed)
Abstract：
Adrenal incidentaloma (AI) is rare and found in approximately 2-4% of abdominal computed tomography scans. Up to 10% of patients with AI have autonomous secretion of adrenal hormones. If not quickly diagnosed and adequately treated, the outcome may be devastating to the patient. On very rare occasions, a pheochromocytoma may, in addition to the production of catecholamine, produce adrenocorticotropic hormone causing Cushing disease. We present a case of a patient with pheochromocytoma and Cushing syndrome.
摘要：
肾上腺偶发瘤（AI）很少见，在大约2-4％的腹部计算机断层扫描中发现。高达10%的AI患者自主分泌肾上腺激素。如果不能迅速诊断和充分治疗，结果可能会给病人带来毁灭性的打击.在非常罕见的情况下，嗜铬细胞瘤，除了生产儿茶酚胺，产生促肾上腺皮质激素引起库欣病。我们介绍了一例嗜铬细胞瘤和库欣综合征的患者。
