Matheny Leslee N, Wilson Jessica R, Baum Howard B A
Vanderbilt University Medical Center, Nashville, TN, USA.
J Investig Med High Impact Case Rep. 2016 Apr 8;4(2):2324709616643989. doi: 10.1177/2324709616643989. eCollection 2016 Apr-Jun.
Medullary thyroid carcinoma (MTC) has been described as a source of ectopic ACTH secretion in patients with Cushing's syndrome. This is an infrequent association, occurring in less than 1% of MTC cases. Among these, it is even more unusual for an initial diagnosis of hypercortisolism to lead to the discovery of underlying MTC. Here we present a case of a patient with weakness, diarrhea, and hypokalemia who was found first to have Cushing's syndrome and later diagnosed with metastatic MTC. The patient was treated initially with oral agents to control his hypercortisolism, then with an etomidate infusion after experiencing intestinal perforation. He also received vandetanib therapy targeting his underlying malignancy, as this has been shown to reverse clinical signs of Cushing's syndrome in patients with MTC and subsequent ectopic ACTH secretion. Bilateral adrenalectomy was ultimately required. Medullary thyroid carcinoma should be considered in patients presenting with Cushing's syndrome due to ectopic ACTH secretion, and a multimodality treatment approach is often required.
甲状腺髓样癌(MTC)被描述为库欣综合征患者异位促肾上腺皮质激素(ACTH)分泌的来源。这种关联并不常见,在不到1%的MTC病例中出现。其中,因皮质醇增多症的初始诊断而发现潜在MTC的情况更为罕见。在此,我们报告一例患者,该患者有乏力、腹泻和低钾血症,最初被诊断为库欣综合征,后来被诊断为转移性MTC。患者最初接受口服药物治疗以控制皮质醇增多症,在出现肠穿孔后接受依托咪酯输注治疗。他还接受了针对其潜在恶性肿瘤的凡德他尼治疗,因为已证明这种治疗可逆转MTC及随后异位ACTH分泌患者的库欣综合征临床体征。最终需要进行双侧肾上腺切除术。对于因异位ACTH分泌而出现库欣综合征的患者,应考虑甲状腺髓样癌,且通常需要采取多模式治疗方法。