Alwani R A, Neggers S J C M M, van der Klift M, Baggen M G A, van Leenders G J L H, van Aken M O, van der Lely A J, de Herder W W, Feelders R A
Department of Internal Medicine, Endocrine Section, Rotterdam, The Netherlands.
Pituitary. 2009;12(3):280-3. doi: 10.1007/s11102-008-0100-z.
Ectopic adrenocorticotropin (ACTH) secretion accounts for less than 10% of all causes of endogenous Cushing's syndrome (CS) and is usually associated with neuroendocrine tumors and small cell carcinoma of the lung. We report the case of a 62-year-old man with CS due to ectopic ACTH production by small cell carcinoma of the prostate. He presented with severe hypercortisolism and associated symptoms. Plasma neuron specific enolase (NSE) was grossly elevated. Despite performing a laparoscopic bilateral adrenalectomy, the patient died as a result of sepsis with multi-organ failure. Post-mortem immunohistochemical staining of prostate tumor tissue showed ACTH expression. ACTH staining was also performed in four additional patients with small cell carcinoma of the urinary tract without CS. None of these additional cases showed a positive staining for ACTH. Although a rare cause of ectopic ACTH production, neuroendocrine prostate carcinoma should be considered in male patients with Cushing's syndrome, in particular in those with an occult source of ACTH overproduction.
异位促肾上腺皮质激素(ACTH)分泌占内源性库欣综合征(CS)所有病因的比例不到10%,通常与神经内分泌肿瘤和肺小细胞癌有关。我们报告了一例62岁男性因前列腺小细胞癌异位分泌ACTH导致CS的病例。他表现出严重的皮质醇增多症及相关症状。血浆神经元特异性烯醇化酶(NSE)显著升高。尽管进行了腹腔镜双侧肾上腺切除术,但患者因败血症伴多器官衰竭死亡。前列腺肿瘤组织的尸检免疫组化染色显示有ACTH表达。对另外四名无CS的尿路小细胞癌患者也进行了ACTH染色。这些额外病例均未显示ACTH染色阳性。尽管异位ACTH分泌是一种罕见病因,但对于患有库欣综合征的男性患者,尤其是那些ACTH分泌过多来源不明的患者,应考虑神经内分泌前列腺癌。