Anthoney D A, Dunlop D J, Connell J M, Kaye S B
Beatson Oncology Centre, Glasgow, U.K.
Eur J Cancer. 1995 Nov;31A(12):2109-12. doi: 10.1016/0959-8049(95)00388-6.
A 57-year-old woman developed features of Cushing's syndrome after resection of a Duke's C adenocarcinoma of the sigmoid colon. Biochemical and endocrine investigation indicated ectopic production of adrenocorticotrophic hormone (ACTH) as the cause for her condition. Hepatic metastases were detected by computed tomography (CT) scan. Histology of the original tumour displayed neuroendocrine characteristics but no definite evidence of ACTH synthesis. Treatment was instituted to control her hypercortisolism, and chemotherapy initiated to reduce the production of ectopic hormone. A clinical, biochemical and radiological response was obtained with complete resolution of her Cushing's syndrome. The tumour relapsed after several months with distant metastases, but no further endocrine abnormality was noted. A review of ectopic ACTH producing adenocarcinoma is given along with a discussion of the major pathological and therapeutic features of the case.
一名57岁女性在乙状结肠杜克C期腺癌切除术后出现库欣综合征的症状。生化和内分泌检查表明,促肾上腺皮质激素(ACTH)异位分泌是导致其病情的原因。通过计算机断层扫描(CT)检测到肝转移。原发肿瘤的组织学检查显示具有神经内分泌特征,但未发现明确的ACTH合成证据。采取治疗措施控制其高皮质醇血症,并开始化疗以减少异位激素的产生。患者的库欣综合征得到完全缓解,获得了临床、生化和影像学方面的改善。几个月后肿瘤复发并伴有远处转移,但未发现进一步的内分泌异常。本文对异位分泌ACTH的腺癌进行了综述,并讨论了该病例的主要病理和治疗特征。