Literature DB >> 19189136

Malignant paraganglioma associated with succinate dehydrogenase subunit B in an 8-year-old child: the age of first screening?

Tamara Prodanov1, Bas Havekes, Katherine L Nathanson, Karen T Adams, Karel Pacak.   

Abstract

Several studies have shown that patients with succinate dehydrogenase subunit B (SDHB) mutations have a very high risk for developing malignant paragangliomas. However, there is no consensus of what age screening for paragangliomas should start. We report a case of an 8-year-old white girl with a 3-year history of catecholamine excess-related complaints who was diagnosed with a malignant SDHB-associated mediastinal paraganglioma. The patient presented with intermittent sweating, headache, nausea, vomiting, fatigue and weight loss that had been present since she was 5 years of age. A large posterior mediastinal mass measuring 6.4 cm x 3.1 cm x 4.6 cm was discovered on computed tomography (CT) and magnetic resonance imaging (MRI). Laboratory data included an elevated level of urine normetanephrine of 45,400 microg/g creatinine (upper reference limit 718 microg/g) and elevated level of plasma normetanephrine of 62.4 nmol/l (upper reference limit <0.90 nmol/l). She was diagnosed with a thoracic paraganglioma and subsequently underwent surgical removal of the tumor and two lymph nodes. Histopathologic examination confirmed metastatic paraganglioma. Postoperatively, her blood pressure normalized and plasma normetanephrine levels remained normal. Our patient first presented with paraganglioma-associated signs and symptoms at the young age of 5 years. This case clearly illustrates the need for increased vigilance and screening for paragangliomas in families with SDHB at a younger age than previously thought.

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Year:  2009        PMID: 19189136      PMCID: PMC4714580          DOI: 10.1007/s00467-008-1111-8

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  19 in total

1.  Clinical presentations, biochemical phenotypes, and genotype-phenotype correlations in patients with succinate dehydrogenase subunit B-associated pheochromocytomas and paragangliomas.

Authors:  Henri J L M Timmers; Anna Kozupa; Graeme Eisenhofer; Margarita Raygada; Karen T Adams; Daniel Solis; Jacques W M Lenders; Karel Pacak
Journal:  J Clin Endocrinol Metab       Date:  2007-01-02       Impact factor: 5.958

2.  Editorial: paraganglioma--all in the family.

Authors:  William F Young; Abbie L Abboud
Journal:  J Clin Endocrinol Metab       Date:  2006-03       Impact factor: 5.958

3.  The relationship between enzyme activity and the catecholamine content and secretion of pheochromocytomas.

Authors:  J M Feldman; J A Blalock; R T Zern; S A Wells
Journal:  J Clin Endocrinol Metab       Date:  1979-09       Impact factor: 5.958

Review 4.  Genetic basis of phaeochromocytoma and paraganglioma.

Authors:  Diana E Benn; Bruce G Robinson
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2006-09       Impact factor: 4.690

5.  Pheochromocytoma and paraganglioma in children: a review of medical and surgical management at a tertiary care center.

Authors:  Tuan H Pham; Christopher Moir; Geoffrey B Thompson; Abdalla E Zarroug; Chad E Hamner; David Farley; Jon van Heerden; Aida N Lteif; William F Young
Journal:  Pediatrics       Date:  2006-09       Impact factor: 7.124

6.  Characteristics of pheochromocytoma in a 4- to 20-year-old population.

Authors:  Marta Barontini; Gloria Levin; Gabriela Sanso
Journal:  Ann N Y Acad Sci       Date:  2006-08       Impact factor: 5.691

7.  Genetic testing in pheochromocytoma or functional paraganglioma.

Authors:  Laurence Amar; Jérôme Bertherat; Eric Baudin; Christiane Ajzenberg; Brigitte Bressac-de Paillerets; Olivier Chabre; Bernard Chamontin; Brigitte Delemer; Sophie Giraud; Arnaud Murat; Patricia Niccoli-Sire; Stéphane Richard; Vincent Rohmer; Jean-Louis Sadoul; Laurence Strompf; Martin Schlumberger; Xavier Bertagna; Pierre-François Plouin; Xavier Jeunemaitre; Anne-Paule Gimenez-Roqueplo
Journal:  J Clin Oncol       Date:  2005-12-01       Impact factor: 44.544

8.  Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

Authors:  Diana E Benn; Anne-Paule Gimenez-Roqueplo; Jennifer R Reilly; Jérôme Bertherat; John Burgess; Karen Byth; Michael Croxson; Patricia L M Dahia; Marianne Elston; Oliver Gimm; David Henley; Philippe Herman; Victoria Murday; Patricia Niccoli-Sire; Janice L Pasieka; Vincent Rohmer; Kathy Tucker; Xavier Jeunemaitre; Deborah J Marsh; Pierre-François Plouin; Bruce G Robinson
Journal:  J Clin Endocrinol Metab       Date:  2005-11-29       Impact factor: 5.958

9.  Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.

Authors:  Hartmut P H Neumann; Christian Pawlu; Mariola Peczkowska; Birke Bausch; Sarah R McWhinney; Mihaela Muresan; Mary Buchta; Gerlind Franke; Joachim Klisch; Thorsten A Bley; Stefan Hoegerle; Carsten C Boedeker; Giuseppe Opocher; Jörg Schipper; Andrzej Januszewicz; Charis Eng
Journal:  JAMA       Date:  2004-08-25       Impact factor: 56.272

10.  Diagnosis at dusk: malignant hypertension and phaeochromocytoma in a 6-year-old girl.

Authors:  John Corcoran; Chris Bird; Lucy Side; Kokila Lakhoo; Fiona Ryan
Journal:  Emerg Med Australas       Date:  2008-02       Impact factor: 2.151

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  9 in total

1.  Counseling patients with succinate dehydrogenase subunit defects: genetics, preventive guidelines, and dealing with uncertainty.

Authors:  Margarita Raygada; Kathryn S King; Karen T Adams; Constantine A Stratakis; Karel Pacak
Journal:  J Pediatr Endocrinol Metab       Date:  2014-09       Impact factor: 1.634

Review 2.  Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.

Authors:  Lauren Fishbein; Katherine L Nathanson
Journal:  Cancer Genet       Date:  2012 Jan-Feb

3.  Phaeochromocytoma: a catecholamine and oxidative stress disorder.

Authors:  K Pacak
Journal:  Endocr Regul       Date:  2011-04

4.  Pheochromocytoma and paraganglioma.

Authors:  Vitaly Kantorovich; Karel Pacak
Journal:  Prog Brain Res       Date:  2010       Impact factor: 2.453

Review 5.  SDH-related pheochromocytoma and paraganglioma.

Authors:  Vitaly Kantorovich; Kathryn S King; Karel Pacak
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2010-06       Impact factor: 4.690

6.  SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations.

Authors:  Ivana Jochmanova; Katherine I Wolf; Kathryn S King; Joan Nambuba; Robert Wesley; Victoria Martucci; Margarita Raygada; Karen T Adams; Tamara Prodanov; Antonio Tito Fojo; Ivica Lazurova; Karel Pacak
Journal:  J Cancer Res Clin Oncol       Date:  2017-04-03       Impact factor: 4.553

7.  Succinate dehydrogenase gene mutations are strongly associated with paraganglioma of the organ of Zuckerkandl.

Authors:  Maya B Lodish; Karen T Adams; Thanh T Huynh; Tamara Prodanov; Alex Ling; Clara Chen; Suzanne Shusterman; Camilo Jimenez; Maria Merino; Marybeth Hughes; Kendall W Cradic; Dragana Milosevic; Ravinder J Singh; Constantine A Stratakis; Karel Pacak
Journal:  Endocr Relat Cancer       Date:  2010-06-03       Impact factor: 5.678

Review 8.  Clinical Practice Guidance: Surveillance for phaeochromocytoma and paraganglioma in paediatric succinate dehydrogenase gene mutation carriers.

Authors:  Mei Yin Wong; Katrina A Andrews; Benjamin G Challis; Soo-Mi Park; Carlo L Acerini; Eamonn R Maher; Ruth T Casey
Journal:  Clin Endocrinol (Oxf)       Date:  2019-01-29       Impact factor: 3.478

9.  Sporadic paraganglioma caused by de novo SDHB mutations in a 6-year-old girl.

Authors:  Hideaki Imamura; Koji Muroya; Etsuko Tanaka; Takao Konomoto; Hiroshi Moritake; Takeshi Sato; Noriko Kimura; Kazuhiro Takekoshi; Hiroyuki Nunoi
Journal:  Eur J Pediatr       Date:  2015-08-19       Impact factor: 3.183

  9 in total

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