Streuli Regina, Krull Ina, Brändle Michael, Kolb Walter, Stalla Günter, Theodoropoulou Marily, Enzler-Tschudy Annette, Bilz Stefan
Division of Endocrinology and Diabetes, Department of Internal Medicine.
Department of Surgery, Kantonsspital St Gallen, St GallenSwitzerland.
Endocrinol Diabetes Metab Case Rep. 2017 Jun 16;2017. doi: 10.1530/EDM-17-0058. eCollection 2017.
Ectopic ACTH/CRH co-secreting tumors are a very rare cause of Cushing's syndrome and only a few cases have been reported in the literature. Differentiating between Cushing's disease and ectopic Cushing's syndrome may be particularly difficult if predominant ectopic CRH secretion leads to pituitary corticotroph hyperplasia that may mimic Cushing's disease during dynamic testing with both dexamethasone and CRH as well as bilateral inferior petrosal sinus sampling (BIPSS). We present the case of a 24-year-old man diagnosed with ACTH-dependent Cushing's syndrome caused by an ACTH/CRH co-secreting midgut NET. Both high-dose dexamethasone testing and BIPSS suggested Cushing's disease. However, the clinical presentation with a rather rapid onset of cushingoid features, hyperpigmentation and hypokalemia led to the consideration of ectopic ACTH/CRH-secretion and prompted a further workup. Computed tomography (CT) of the abdomen revealed a cecal mass which was identified as a predominantly CRH-secreting neuroendocrine tumor. To the best of our knowledge, this is the first reported case of an ACTH/CRH co-secreting tumor of the cecum presenting with biochemical features suggestive of Cushing's disease.
The discrimination between a Cushing's disease and ectopic Cushing's syndrome is challenging and has many caveats.Ectopic ACTH/CRH co-secreting tumors are very rare.Dynamic tests as well as BIPSS may be compatible with Cushing's disease in ectopic CRH-secretion.High levels of CRH may induce hyperplasia of the corticotroph cells in the pituitary. This could be the cause of a preserved pituitary response to dexamethasone and CRH.Clinical features of ACTH-dependent hypercortisolism with rapid development of Cushing's syndrome, hyperpigmentation, high circulating levels of cortisol with associated hypokalemia, peripheral edema and proximal myopathy should be a warning flag of ectopic Cushing's syndrome and lead to further investigations.
异位促肾上腺皮质激素(ACTH)/促肾上腺皮质激素释放激素(CRH)共分泌肿瘤是库欣综合征非常罕见的病因,文献中仅报道了少数病例。如果主要的异位CRH分泌导致垂体促肾上腺皮质激素细胞增生,在使用地塞米松和CRH进行动态试验以及双侧岩下窦采血(BIPSS)时,可能会模拟库欣病,那么区分库欣病和异位库欣综合征可能特别困难。我们报告一例24岁男性,诊断为ACTH/CRH共分泌的中肠神经内分泌肿瘤(NET)所致的ACTH依赖性库欣综合征。高剂量地塞米松试验和BIPSS均提示库欣病。然而,临床表现为库欣样特征迅速出现、色素沉着和低钾血症,促使考虑异位ACTH/CRH分泌,并促使进一步检查。腹部计算机断层扫描(CT)显示盲肠肿块,经鉴定为主要分泌CRH的神经内分泌肿瘤。据我们所知,这是首例报告的盲肠ACTH/CRH共分泌肿瘤,其生化特征提示库欣病。
区分库欣病和异位库欣综合征具有挑战性且有许多注意事项。异位ACTH/CRH共分泌肿瘤非常罕见。在异位CRH分泌时,动态试验以及BIPSS可能与库欣病相符。高水平的CRH可能诱导垂体促肾上腺皮质激素细胞增生。这可能是垂体对地塞米松和CRH仍有反应的原因。ACTH依赖性皮质醇增多症的临床特征为库欣综合征迅速发展、色素沉着、皮质醇循环水平高伴低钾血症、外周水肿和近端肌病,应警惕异位库欣综合征,并促使进一步检查。