Endocr Pract. 2018 Jan;24(1):78-90. doi: 10.4158/EP-2017-0057. Epub 2017 Nov 16.
Pheochromocytomas and paragangliomas (PPGLs) are neuroendocrine tumors derived from adrenal or extra-adrenal locations, respectively. Upon suspicion of PPGL, specific metabolomic, molecular, biochemical, imaging, and histopathologic studies are performed to prove, localize, treat, and monitor disease progression. Improved diagnostic tools allow physicians to accurately diagnose PPGL, even in patients presenting with small (<1 cm) or biochemically silent tumors, which previously delayed proper detection and treatment.
This review outlines the most updated approach to PPGL patients and presents a new diagnostic protocol for physicians to increase earlier tumor identification and accurately assess metastatic behavior.
We present the most recent advances in genetics, epigenetics, metabolomics, biochemical, and imaging diagnoses of this rare tumor to properly assess disease, decide treatment options, and manage follow-up. We also elaborate on new therapeutic perspectives in these very rare neoplastic entities.
ATRX = ATRX chromatin remodeler; ccRCC = clear cell renal cell carcinoma; c-MYC = MYC proto oncognene; CT = computed tomography; DOTATATE = DOTA-octreotate; EGLN1/2 = egl-9 family hypoxia inducible factor 1/2; EGLN2/PHD1 = egl-9 family hypoxia inducible factor 2; EPAS1/HIF2A = endothelial PAS domain protein 2/hypoxia-inducible factor 2α; ERK = extracellular signal-regulated kinase; HIFs = hypoxia-inducible factors; HIF-α = hypoxia-inducible factor alpha; HNPGLs = head and neck paragangliomas; Lu-DOTATATE = lutetium octreotate; MAX = myc-associated factor X; MDH2 = malate dehydrogenase; MIBG = metaiodobenzylguanidine; MN = metanephrine; MRI = magnetic resonance imaging; mTOR = mammalian target of rapamycin; NETs = neuroendocrine tumors; NF1 = neurofibromin 1; NMN = normetanephrine; PHD = prolyl hydroxylase domain protein; PI3K = phosphoinositide 3-kinase; PPGLs = pheochromocytoma and paragangliomas; PRRT = peptide receptor radionuclide therapy; Pvhl = von Hippel-Lindau protein; RAS = rat sarcoma oncogene; RET = rearranged during transfection proto-oncogene; SDH = succinate dehydrogenase; SDHA, -B, -C, -D = succinate dehydrogenase subunits A, B, C, D; SDHAF2 = succinate dehydrogenase complex assembly factor 2; SDHB, C, D = succinate dehydrogenase subunits B, C, D; SDHx = succinate dehydrogenase subunits; SSTRs = somatostatin receptors; VHL = von Hippel-Lindau.
嗜铬细胞瘤和副神经节瘤(PPGLs)分别起源于肾上腺或肾上腺外部位的神经内分泌肿瘤。怀疑患有 PPGL 时,需要进行特定的代谢组学、分子、生化、影像学和组织病理学研究,以证实、定位、治疗和监测疾病进展。改进的诊断工具使医生能够准确诊断 PPGL,即使是在有小(<1cm)或生化无明显表现的肿瘤的患者中,这些肿瘤以前会延迟适当的检测和治疗。
本综述概述了 PPGL 患者的最新方法,并提出了一种新的诊断方案,以提高肿瘤的早期识别能力,并准确评估转移行为。
我们介绍了这种罕见肿瘤在遗传学、表观遗传学、代谢组学、生化和影像学诊断方面的最新进展,以便对疾病进行适当评估、决定治疗选择并进行随访管理。我们还详细阐述了这些非常罕见的肿瘤实体中新的治疗前景。
ATRX = ATRX 染色质重塑剂;ccRCC = 透明细胞肾细胞癌;c-MYC = MYC 原癌基因;CT = 计算机断层扫描;DOTATATE = DOTA-奥曲肽;EGLN1/2 = egl-9 家族缺氧诱导因子 1/2;EGLN2/PHD1 = egl-9 家族缺氧诱导因子 2;EPAS1/HIF2A = 内皮 PAS 结构域蛋白 2/缺氧诱导因子 2α;ERK = 细胞外信号调节激酶;HIFs = 缺氧诱导因子;HIF-α = 缺氧诱导因子 alpha;HNPGLs = 头颈部副神经节瘤;Lu-DOTATATE = 镥奥曲肽;MAX = myc 相关因子 X;MDH2 = 苹果酸脱氢酶 2;MIBG = 间碘苄胍;MN = 间甲肾上腺素;MRI = 磁共振成像;mTOR = 哺乳动物雷帕霉素靶蛋白;NETs = 神经内分泌肿瘤;NF1 = 神经纤维瘤蛋白 1;NMN = 去甲肾上腺素;PHD = 脯氨酰羟化酶结构域蛋白;PI3K = 磷酸肌醇 3-激酶;PPGLs = 嗜铬细胞瘤和副神经节瘤;PRRT = 肽受体放射性核素治疗;Pvhl = 血管母细胞瘤蛋白;RAS = 大鼠肉瘤癌基因;RET = 转染重排原癌基因;SDH = 琥珀酸脱氢酶;SDHA、-B、-C、-D = 琥珀酸脱氢酶亚基 A、B、C、D;SDHAF2 = 琥珀酸脱氢酶复合物组装因子 2;SDHB、C、D = 琥珀酸脱氢酶亚基 B、C、D;SDHx = 琥珀酸脱氢酶亚基;SSTRs = 生长抑素受体;VHL = 血管母细胞瘤蛋白。