Loh K C, Gupta R, Shlossberg A H
Division of Endocrinology and Metabolism, Dalhousie University, Halifax, Canada.
Eur J Endocrinol. 1996 Oct;135(4):440-3. doi: 10.1530/eje.0.1350440.
A young female adult with Cushing's syndrome arising from ectopic production of corticotropin (ACTH) from an adrenal pheochromocytoma showed spontaneous clinical and biochemical remission of hypercortisolism after a brief period of ketoconazole administration. Despite continued remission of the hypercortisolism over the next 18 months, there was progressive catecholamine hypersecretion with significant morbidity as a result of the pheochromocytoma. Surgical resection of the left adrenal gland revealed a pheochromocytoma showing focal cytoplasmic immunostaining for ACTH and marked diffuse compact cell hyperplasia in the adrenocortical tissue. To our knowledge this is the first reported case of spontaneous clinical and biochemical remission of ectopic ACTH production from a pheochromocytoma. The pathogenesis of the remission remains unknown.
一名年轻成年女性因肾上腺嗜铬细胞瘤异位分泌促肾上腺皮质激素(ACTH)而患有库欣综合征,在短期服用酮康唑后,出现了高皮质醇血症的自发临床和生化缓解。尽管在接下来的18个月中高皮质醇血症持续缓解,但嗜铬细胞瘤导致儿茶酚胺分泌进行性增多,并伴有明显的发病率。左侧肾上腺手术切除显示为嗜铬细胞瘤,其ACTH呈局灶性细胞质免疫染色,肾上腺皮质组织有明显弥漫性致密细胞增生。据我们所知,这是首例报道的嗜铬细胞瘤异位ACTH分泌自发临床和生化缓解的病例。缓解的发病机制尚不清楚。