Urinary 5-HIAA excretion is not increased in patients with head and neck paragangliomas.

作者: Leonie T. Van Hulsteijn , Nicolette Van Duinen , Johannes A. Romijn , Johannes W.A. Smit , Eleonora P.M. Corssmit

DOI: 10.5301/JBM.2012.9312

关键词: Internal medicineEpinephrineNormetanephrineEndocrinologyReference rangeUrinary systemUrineMetanephrineHormoneMedicineExcretion

摘要: Background: Case reports have documented carcinoid-like features in head and neck paragangliomas (HNPGLs), which, addition to catecholamine storing granules, may also contain granules with serotonin. Serotonin is metabolized 5-hydroxyindoleacetic acid (5-HIAA). Aim: To assess the urinary excretion rates of 5-HIAA catecholamines HNPGL patients.Methods: In 114 consecutive patients, normetanephrine, metanephrine, norepinephrine, epinephrine, VMA, dopamine, 3-methoxytyramine were measured two 24-hour samples. Increased defined as an increase average hormone rate 2 urine samples above reference range. all patients excess, intrathoracic abdominal excluded by 123I-MIBG scintigraphy, MRI and/or CT. Genetic screening for mutations genes succinate dehydrogenase (SDH) family was performed. Results: Mean 14+/-9 mumol/24 hours (reference range 10-44 hours). Urinary slightly increased only 1 patient (48 None 50 (44%) their metabolites had elevated excretion.Conclusion: within normal almost patients. Therefore, this parameter has no clinical relevance routine assessment

参考文章(16)
Nicolette van Duinen, Ido P. Kema, Johannes A. Romijn, Eleonora P.M. Corssmit, Plasma chromogranin A levels are increased in a small portion of patients with hereditary head and neck paragangliomas Clinical Endocrinology. ,vol. 74, pp. 160- 165 ,(2011) , 10.1111/J.1365-2265.2010.03914.X
Ido P. Kema, Gert Meiborg, Gijs T. Nagel, Gerrie J. Stob, Frits A.J. Muskiet, Isotope dilution ammonia chemical ionization mass fragmentographic analysis of urinary 3-O-methylated catecholamine metabolites: Rapid sample clean-up by derivatization and extraction of lyophilized samples Journal of Chromatography B: Biomedical Sciences and Applications. ,vol. 617, pp. 181- 189 ,(1993) , 10.1016/0378-4347(93)80486-N
Jay B. Farrior, James T. Packer, Glomus tumors of the temporal bone: electron microscopic and immunohistochemical evaluation. Otolaryngology-Head and Neck Surgery. ,vol. 104, pp. 24- 28 ,(1991) , 10.1177/019459989110400106
Aaron I Vinik, Eugene A Woltering, Richard RP Warner, Martyn Caplin, Thomas M O'Dorisio, Gregory A Wiseman, Domenico Coppola, Vay Liang W Go, None, NANETS Consensus Guidelines for the Diagnosis of Neuroendocrine Tumor Pancreas. ,vol. 39, pp. 713- 734 ,(2010) , 10.1097/MPA.0B013E3181EBAFFD
RF Badenhop, JC Jansen, Paul Anthony Fagan, RSA Lord, ZG Wang, WJ Foster, PR Schofield, The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical features Journal of Medical Genetics. ,vol. 41, pp. 1- 5 ,(2004) , 10.1136/JMG.2003.011551
N. van Duinen, D. Steenvoorden, I. P. Kema, J. C. Jansen, A. H. J. T. Vriends, J. P. Bayley, J. W. A. Smit, J. A. Romijn, E. P. M. Corssmit, Increased Urinary Excretion of 3-Methoxytyramine in Patients with Head and Neck Paragangliomas The Journal of Clinical Endocrinology and Metabolism. ,vol. 95, pp. 209- 214 ,(2010) , 10.1210/JC.2009-1632
Peter E.M. Taschner, Jeroen C. Jansen, Bora E. Baysal, Anne Bosch, Efraim H. Rosenberg, Annette H.J.T. Bröcker-Vriends, Andel G.L. van der Mey, Gert-Jan B. van Ommen, Cees J. Cornelisse, Peter Devilee, Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene Genes, Chromosomes and Cancer. ,vol. 31, pp. 274- 281 ,(2001) , 10.1002/GCC.1144
Wim G Meijer, Ido P Kema, Marcel Volmer, Pax H B Willemse, Elisabeth G E de Vries, Discriminating Capacity of Indole Markers in the Diagnosis of Carcinoid Tumors Clinical Chemistry. ,vol. 46, pp. 1588- 1596 ,(2000) , 10.1093/CLINCHEM/46.10.1588
Karel Pacak, Graeme Eisenhofer, Håkan Ahlman, Stefan R Bornstein, Anne-Paule Gimenez-Roqueplo, Ashley B Grossman, Noriko Kimura, Massimo Mannelli, Anne Marie McNicol, Arthur S Tischler, Pheochromocytoma: recommendations for clinical practice from the First International Symposium Nature Clinical Practice Endocrinology & Metabolism. ,vol. 3, pp. 92- 102 ,(2007) , 10.1038/NCPENDMET0396