Literature DB >> 15365827

Multiple pheochromocytomas and paragangliomas in a young patient carrying a SDHD gene mutation.

Astrid Novosel1, Alfred Heger, Peter Lohse, Heinrich Schmidt.   

Abstract

UNLABELLED: We report a 13-year-old boy with an atypical manifestation of a multilocular paraganglioma. Surgical treatment was not curative despite extirpation of a left-sided abdominal paraganglioma. After surgery, the boy experienced several hypertensive crises. Further investigations including dopamine-positron emission tomography demonstrated bilateral adrenal tumours, a further right-sided paravertebral tumour as well as bilateral cervical glomus tumours. Genetic testing revealed a germline mutation in the succinate dehydrogenase subunit D (SDHD) gene.
CONCLUSION: The final diagnosis was familial pheochromocytoma/paraganglioma type 1 (OMIM 168000). Antihypertensive treatment was succesfull and improved the patient's quality of life.

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Year:  2004        PMID: 15365827     DOI: 10.1007/s00431-004-1538-2

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  13 in total

1.  Germline SDHD mutation in familial phaeochromocytoma.

Authors:  D Astuti; F Douglas; T W Lennard; I A Aligianis; E R Woodward; D G Evans; C Eng; F Latif; E R Maher
Journal:  Lancet       Date:  2001-04-14       Impact factor: 79.321

2.  Change of left ventricular geometric pattern after 1 year of antihypertensive treatment: the Losartan Intervention For Endpoint reduction in hypertension (LIFE) study.

Authors:  Kristian Wachtell; Björn Dahlöf; Jens Rokkedal; Vasilious Papademetriou; Markku S Nieminen; Gunnar Smith; Eva Gerdts; Kurt Boman; Jonathan N Bella; Richard B Devereux
Journal:  Am Heart J       Date:  2002-12       Impact factor: 4.749

3.  Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma.

Authors:  D Astuti; F Latif; A Dallol; P L Dahia; F Douglas; E George; F Sköldberg; E S Husebye; C Eng; E R Maher
Journal:  Am J Hum Genet       Date:  2001-06-12       Impact factor: 11.025

4.  Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.

Authors:  P E Taschner; J C Jansen; B E Baysal; A Bosch; E H Rosenberg; A H Bröcker-Vriends; A G van Der Mey; G J van Ommen; C J Cornelisse; P Devilee
Journal:  Genes Chromosomes Cancer       Date:  2001-07       Impact factor: 5.006

5.  Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.

Authors:  R F Badenhop; S Cherian; R S Lord; B E Baysal; P E Taschner; P R Schofield
Journal:  Genes Chromosomes Cancer       Date:  2001-07       Impact factor: 5.006

Review 6.  Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma.

Authors:  K Pacak; W M Linehan; G Eisenhofer; M M Walther; D S Goldstein
Journal:  Ann Intern Med       Date:  2001-02-20       Impact factor: 25.391

7.  Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.

Authors:  B E Baysal; J E Farr; W S Rubinstein; R A Galus; K A Johnson; C E Aston; E N Myers; J T Johnson; R Carrau; S J Kirkpatrick; D Myssiorek; D Singh; S Saha; S M Gollin; G A Evans; M R James; C W Richard
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

8.  Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

Authors:  S Niemann; U Müller
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

9.  Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma.

Authors:  J M Milunsky; T A Maher; V V Michels; A Milunsky
Journal:  Am J Med Genet       Date:  2001-05-15

Review 10.  Pheochromocytoma: the expanding genetic differential diagnosis.

Authors:  Jennifer Bryant; Jennifer Farmer; Lisa J Kessler; Raymond R Townsend; Katherine L Nathanson
Journal:  J Natl Cancer Inst       Date:  2003-08-20       Impact factor: 13.506

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  2 in total

Review 1.  SDH mutations in tumorigenesis and inherited endocrine tumours: lesson from the phaeochromocytoma-paraganglioma syndromes.

Authors:  B Pasini; C A Stratakis
Journal:  J Intern Med       Date:  2009-07       Impact factor: 8.989

Review 2.  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

  2 in total

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