作者: Nicolette van Duinen , Ido P. Kema , Johannes A. Romijn , Eleonora P.M. Corssmit
DOI: 10.1111/J.1365-2265.2010.03914.X
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摘要: Summary Context The majority of patients with head and neck paragangliomas (HNPGL) have biochemically silent tumours. Chromogranin A (CgA) is a tumour marker for neuroendocrine tumours. Objective To assess the role CgA as in hereditary HNPGL. Patients Methods We included 95 consecutive HNPGL screening plasma levels catecholamine excess by measurement 24-h urinary excretion (nor)metanephrine, (nor)adrenaline, VMA, dopamine 3-methoxytyramine. In all excess, abdominal/intrathoracic were excluded 123I-MIBG scintigraphy, MRI and/or CT. Results Plasma increased only 15 (16%). Thirty-three (35%) had rates catecholamines. Six these 33 (18%) levels. Nine 62 (15%) tumour, i.e. no catecholamines or their metabolites, Increased positively correlated noradrenaline (r = 0·68, P = 0·005) normetanephrine P = 0·005). There was positive correlation between maximal diameter 57 single (r = 0·57, P = 0·001). Conclusions are small portion limited additional value to combination radiological routine biochemical assessment HNPGL. associated noradrenergic activity size