Baas J M, Kapiteijn E, Pereira A M, Nortier J W R
Department of Clinical Oncology, Leiden University Medical Centre, Leiden, the Netherlands.
Neth J Med. 2010 Jun;68(6):265-7.
We present an atypical case of Cushing's syndrome caused by ectopic adrenocorticotropic hormone (ACTH) secretion in a patient with a metastasised adenocarcinoma of the oesophagus. After chemotherapy and surgery the patient developed generalised oedema, hyperpigmentation and dysphagia. Laboratory tests showed hypokalaemia, normal urinary potassium, increased 24-hour urinary free cortisol excretion and serum ACTH within the normal reference range. The diagnosis of ACTH-dependent Cushing's syndrome was made, most probably caused by ectopic production of ACTH. In addition to combined chemotherapy, treatment with ketoconazole sufficiently reduced urinary cortisol excretion and relieved the symptoms.
我们报告了一例由异位促肾上腺皮质激素(ACTH)分泌引起的库欣综合征的非典型病例,患者为一名患有转移性食管癌的患者。化疗和手术后,患者出现全身性水肿、色素沉着和吞咽困难。实验室检查显示低钾血症、尿钾正常、24小时尿游离皮质醇排泄增加以及血清ACTH在正常参考范围内。诊断为ACTH依赖性库欣综合征,很可能是由ACTH的异位产生引起的。除联合化疗外,酮康唑治疗充分降低了尿皮质醇排泄并缓解了症状。