Young William F
Division of Endocrinology, Diabetes, Metabolism, Nutrition, and Internal Medicine, Mayo Clinic, 200 First Street S.W. Rochester, MN 55905, USA.
Ann N Y Acad Sci. 2006 Aug;1073:21-9. doi: 10.1196/annals.1353.002.
Paragangliomas are rare tumors that arise from extra-adrenal paraganglia. The effective diagnosis and management of the paraganglioma patient involves the close collaboration of endocrinologists, endocrine surgeons, anesthesiologists, geneticists, laboratory specialists, radiologists, oncologists, and pathologists. Paragangliomas are diagnosed in the following clinical settings: signs and symptoms related to catecholamine hypersecretion, mass effect symptoms (e.g., with head and neck paragangliomas), incidental finding on imaging, or family screening for hereditary paraganglioma. Paragangliomas that hypersecrete catecholamines may cause signs and symptoms identical to those in patients with hyperfunctioning adrenal pheochromocytoma. When a catecholamine-secreting tumor is suspected in a patient because of paroxysmal symptoms, biochemical documentation of catecholamine and fractionated metanephrine hypersecretion should precede any form of imaging study. Catecholamine-secreting paragangliomas are found where chromaffin tissue is located (e.g., along the para-aortic sympathetic chain, or within the organs of Zuckerkandl at the origin of the inferior mesenteric artery, the wall of the urinary bladder, and the sympathetic chain in the neck or mediastinum). As many as 50% of paragangliomas are hereditary and may be associated with familial paraganglioma, neurofibromatosis Type 1, von Hippel-Lindau disease, the Carney triad, and, rarely, with multiple endocrine neoplasia Type 2. Genetic testing should be considered in all patients with paraganglioma. The treatment of choice for paraganglioma is surgical resection; most tumors are benign and can be excised totally. Following surgical cure, annual biochemical testing assesses for metastatic disease, tumor recurrence or delayed appearance of multiple primary tumors.
副神经节瘤是起源于肾上腺外副神经节的罕见肿瘤。副神经节瘤患者的有效诊断和管理需要内分泌学家、内分泌外科医生、麻醉师、遗传学家、实验室专家、放射科医生、肿瘤学家和病理学家密切合作。副神经节瘤在以下临床情况下被诊断出来:与儿茶酚胺分泌过多相关的体征和症状、占位效应症状(如头颈部副神经节瘤)、影像学检查偶然发现,或遗传性副神经节瘤的家族筛查。分泌过多儿茶酚胺的副神经节瘤可能导致与功能性肾上腺嗜铬细胞瘤患者相同的体征和症状。当因阵发性症状怀疑患者患有分泌儿茶酚胺的肿瘤时,在进行任何形式的影像学检查之前,应先进行儿茶酚胺和分馏甲氧基肾上腺素分泌过多的生化记录。分泌儿茶酚胺的副神经节瘤位于嗜铬组织所在的部位(如腹主动脉旁交感神经链沿线,或肠系膜下动脉起始处的祖克坎德尔器官内、膀胱壁以及颈部或纵隔的交感神经链内)。多达50%的副神经节瘤是遗传性的,可能与家族性副神经节瘤、1型神经纤维瘤病、冯·希佩尔-林道病、卡尼三联征以及罕见的2型多发性内分泌肿瘤有关。所有副神经节瘤患者都应考虑进行基因检测。副神经节瘤的首选治疗方法是手术切除;大多数肿瘤是良性的,可以完全切除。手术治愈后,每年进行生化检测以评估是否有转移性疾病、肿瘤复发或多原发性肿瘤的延迟出现。