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  • Benn, Diana EDepartment of Cancer Genetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney 2006, Australia (författare)

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

  • Artikel/kapitelEngelska2006

Förlag, utgivningsår, omfång ...

  • The Endocrine Society,2006
  • printrdacarrier

Nummerbeteckningar

  • LIBRIS-ID:oai:DiVA.org:liu-101421
  • https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-101421URI
  • https://doi.org/10.1210/jc.2005-1862DOI

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  • Språk:engelska
  • Sammanfattning på:engelska

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Klassifikation

  • Ämneskategori:ref swepub-contenttype
  • Ämneskategori:art swepub-publicationtype

Anmärkningar

  • CONTEXT: The identification of mutations in genes encoding peptides of succinate dehydrogenase (SDH) in pheochromocytoma/paraganglioma syndromes has necessitated clear elucidation of genotype-phenotype associations.OBJECTIVE: Our objective was to determine genotype-phenotype associations in a cohort of patients with pheochromocytoma/paraganglioma syndromes and succinate dehydrogenase subunit B (SDHB) or subunit D (SDHD) mutations.DESIGN, SETTING, AND PARTICIPANTS: The International SDH Consortium studied 116 individuals (83 affected and 33 clinically unaffected) from 62 families with pheochromocytoma/paraganglioma syndromes and SDHB or SDHD mutations. Clinical data were collected between August 2003 and September 2004 from tertiary referral centers in Australia, France, New Zealand, Germany, United States, Canada, and Scotland.MAIN OUTCOME MEASURES: Data were collected on patients with pheochromocytomas and/or paragangliomas with respect to onset of disease, diagnosis, genetic testing, surgery, pathology, and disease progression. Clinical features were evaluated for evidence of genotype-phenotype associations, and penetrance was determined.RESULTS: SDHB mutation carriers were more likely than SDHD mutation carriers to develop extraadrenal pheochromocytomas and malignant disease, whereas SDHD mutation carriers had a greater propensity to develop head and neck paragangliomas and multiple tumors. For the index cases, there was no difference between 43 SDHB and 19 SDHD mutation carriers in the time to first diagnosis (34 vs. 28 yr, respectively; P = 0.3). However, when all mutation carriers were included (n = 112), the estimated age-related penetrance was different for SDHB vs. SDHD mutation carriers (P = 0.008).CONCLUSIONS: For clinical follow-up, features of SDHB mutation-associated disease include a later age of onset, extraadrenal (abdominal or thoracic) tumors, and a higher rate of malignancy. In contrast, SDHD mutation carriers, in addition to head and neck paragangliomas, should be observed for multifocal tumors, infrequent malignancy, and the possibility of extraadrenal pheochromocytoma.

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Gimenez-Roqueplo, Anne-PauleDepartment of Genetics, Hôpital Européen Georges Pompidou, Assistance Publique des Hôpitaux de Paris, L’Institut National de la Santé et de la Recherche Médicale (INSERM) U36, Collège de France, University Paris 5, Paris 75015, France (författare)
  • Reilly, Jennifer RDepartment of Cancer Genetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney 2006, Australia (författare)
  • Bertherat, JérômeDepartment of Endocrinology, INSERM U567, Hôpital Cochin Assistance Publique des Hôpitaux de Paris, University Paris 5, Paris 75014, France (författare)
  • Burgess, JohnDepartment of Endocrinology, Royal Hobart Hospital, Tasmania 7001, Australia (författare)
  • Byth, KarenNational Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney 2006, Australia (författare)
  • Croxson, MichaelDepartment of Endocrinology, Greenlane Clinical Centre, Auckland, New Zealand (författare)
  • Dahia, Patricia L MDepartments of Medicine and Cellular and Structural Biology, University of Texas Health Science Center, San Antonio, Texas 78229-3900 (författare)
  • Elston, MarianneDepartment of Endocrinology, Waikato Hospital, Hamilton, New Zealand (författare)
  • Gimm, OliverDepartment of General, Visceral and Vascular Surgery, Martin Luther University Halle-Wittenberg, Halle 06097, Germany(Swepub:liu)oligi51 (författare)
  • Henley, DavidDepartment of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Western Australia 6009, Australia (författare)
  • Herman, PhilippeDepartment of Otorhinolaryngology and Head and Neck Surgery, Hôpital Lariboisière, Assistance Publique des Hopitaux de Paris, Paris 75010, France (författare)
  • Murday, VictoriaWest of Scotland, Regional Genetics Services, Yorkhill G3 8SJ, Scotland (författare)
  • Niccoli-Sire, PatriciaDepartment of Endocrinology, Hôpital de la Timone, Assistance Publique des Hôpitaux de Marseille, Marseille 13385, France (författare)
  • Pasieka, Janice LDepartment of Surgery, Faculty of Medicine, University of Calgary, Calgary, Canada T2N 1N4 (författare)
  • Rohmer, VincentDepartment of Endocrinology, Hôpital d’Angers, Angers 49033, France (författare)
  • Tucker, KathyHereditary Cancer Clinic, Prince of Wales Hospital and School of Medicine, University of New South Wales, Sydney, New South Wales 2052, Australia (författare)
  • Jeunemaitre, XavierDepartment of Genetics, Hôpital Européen Georges Pompidou, Assistance Publique des Hôpitaux de Paris, L’Institut National de la Santé et de la Recherche Médicale (INSERM) U36, Collège de France, University Paris 5, Paris 75015, France (författare)
  • Marsh, Deborah JDepartment of Cancer Genetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney 2006, Australia (författare)
  • Plouin, Pierre-FrançoisDepartment Hypertension, Hôpital Européen Georges Pompidou, Assistance Publique des Hôpitaux de Paris, L’Institut National de la Santé et de la Recherche Médicale (INSERM) U36, Collège de France, University Paris 5, Paris 75015, France (författare)
  • Robinson, Bruce GDepartment of Endocrinology, Royal North Shore Hospital, Sydney 2065, Australia (författare)
  • Department of Cancer Genetics, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney 2006, AustraliaDepartment of Genetics, Hôpital Européen Georges Pompidou, Assistance Publique des Hôpitaux de Paris, L’Institut National de la Santé et de la Recherche Médicale (INSERM) U36, Collège de France, University Paris 5, Paris 75015, France (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Journal of Clinical Endocrinology and Metabolism: The Endocrine Society91:3, s. 827-360021-972X1945-7197

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