A Case Report of Cortisol-Secreating Adrenal Adenoma Causing Cushing Syndrome

H. Radhi
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Abstract

Cushing syndrome is a state of prolonged exposure to excess cortisol production. Causes can be varied ranging from exogenous intake or endogenous production from a pituitary source due to overproduction of adrenocorticotropic hormone (ACTH) or due to over secretion from unilateral or bilateral adrenal glands. Cushing syndrome in an adult can present with proximal muscle weakness, facial plethora, wasting of the extremities with increased fat in the abdomen and face, wide purplish striae, bruising with no obvious trauma, and supraclavicular fat pads. Here, we report a 38 year old male who presented with suspicion of having Cushing syndrome due to his clinical manifestations and high cortisol levels. He presented to the clinic with new onset diabetes, severe hypertension, chronic abdominal pain and distension which was being investigating by different specialties. The patient underwent CT scan of the abdomen which show right adrenal adenoma and on examination, he was found to have proximal weakness and purple striae. Laboratory data showed high morning cortisol, 24 urine free cortisol and ACTH levels which were strongly suggestive of ACTH independent Cushing syndrome.
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肾上腺皮质醇分泌腺瘤致库欣综合征1例报告
库欣综合征是一种长期暴露于过量皮质醇产生的状态。原因可以是多种多样的,从外源性摄入或内源性产生的垂体源由于过量生产促肾上腺皮质激素(ACTH)或由于过度分泌从单侧或双侧肾上腺。成人库欣综合征可表现为近端肌肉无力,面部过多,四肢消瘦,腹部和面部脂肪增加,宽紫色条纹,无明显创伤的瘀伤,锁骨上脂肪垫。在此,我们报告一位38岁男性,因其临床表现和高皮质醇水平而怀疑患有库欣综合征。他以新发糖尿病、严重高血压、慢性腹痛和腹胀就诊,正在接受不同专科的调查。患者行腹部CT扫描,显示右侧肾上腺腺瘤,检查时发现近端无力及紫色条纹。实验室数据显示早晨皮质醇、24尿游离皮质醇和ACTH水平高,强烈提示ACTH非依赖性库欣综合征。
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