Literature DB >> 27634942

Rapid-sequence MRI for long-term surveillance for paraganglioma and phaeochromocytoma in patients with succinate dehydrogenase mutations.

Eleni Daniel1,2, Robert Jones1,2, Matthew Bull3, John Newell-Price4,2.   

Abstract

BACKGROUND: Patients with SDHx mutations need long-term radiological surveillance for the development of paragangliomas and phaeochromocytomas, but no longitudinal data exist. The aim of the study was to assess the performance of rapid-sequence non-contrast magnetic resonance imaging (MRI) in the long-term monitoring of patients with SDHx mutations.
METHODS: Retrospective study between 2005 and 2015 at a University Hospital and regional endocrine genetics referral centre. Clinical and imaging data of 47 patients with SDHx mutations (SDHB (36), SDHC (6) and SDHD (5)) who had surveillance for detection of paragangliomas by rapid-sequence non-contrast MRI (base of skull to pubic symphysis) were collected.
RESULTS: Twelve index cases (nine SDHB, one SDHC and two SDHD) and 35 mutation-positive relatives were monitored for a mean of 6.4 years (range 3.1-10.0 years). Mean age at the end of the study: SDHB 46.9 ± 17.6 years; SDHC 42.3 ± 24.4 years; SDHD 54.9 ± 10.6 years. On excluding imaging at initial diagnosis of index cases, 42 patients underwent 116 rapid-sequence MRI scans: 83 scans were negative and 31 scans were positive for sPGL/HNPGL in 13 patients. Most patients had multiple scans (n = number of patients (number of rapid-sequence MRI scans during screening)): n = 9 (2), n = 20 (3), n = 6 (4), n = 1 (6). Nine patients (three index) were diagnosed with new paragangliomas during surveillance and non-operated tumour size was monitored in nine patients. There were two false-positive scans (1.6%). Scans were repeated every 27 ± 9 months.
CONCLUSIONS: Biannual rapid-sequence non-contrast MRI is effective to monitor patients with SDHx mutations for detection of new tumours and monitoring of known tumours.
© 2016 European Society of Endocrinology.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27634942     DOI: 10.1530/EJE-16-0595

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  12 in total

1.  Tumor multifocality with vagus nerve involvement as a phenotypic marker of SDHD mutation in patients with head and neck paragangliomas: A 18 F-FDOPA PET/CT study.

Authors:  Vincent Amodru; Pauline Romanet; Ugo Scemama; Marion Montava; Nicolas Fakhry; Frédéric Sebag; Frédéric Castinetti; Jean-Pierre Lavieille; Anderson Loundou; Arthur Varoquaux; Anne Barlier; Karel Pacak; David Taïeb
Journal:  Head Neck       Date:  2018-12-24       Impact factor: 3.147

2.  European Association of Nuclear Medicine Practice Guideline/Society of Nuclear Medicine and Molecular Imaging Procedure Standard 2019 for radionuclide imaging of phaeochromocytoma and paraganglioma.

Authors:  David Taïeb; Rodney J Hicks; Elif Hindié; Benjamin A Guillet; Anca Avram; Pietro Ghedini; Henri J Timmers; Aaron T Scott; Saeed Elojeimy; Domenico Rubello; Irène J Virgolini; Stefano Fanti; Sona Balogova; Neeta Pandit-Taskar; Karel Pacak
Journal:  Eur J Nucl Med Mol Imaging       Date:  2019-06-29       Impact factor: 9.236

3.  A need to tailor surveillance based on family history: describing a highly penetrant familial paraganglioma kindred with an SDHD pathogenic variant.

Authors:  Madeline Foley; Anu Sharma; Kinley Garfield; Luke Maese; Luke Buchmann; Julie Boyle; Wendy Kohlmann; Joanne Jeter; Samantha Greenberg
Journal:  Fam Cancer       Date:  2022-10-12       Impact factor: 2.446

Review 4.  Diagnostic Investigation of Lesions Associated with Succinate Dehydrogenase Defects.

Authors:  David Taïeb; Henri Timmers; Karel Pacak
Journal:  Horm Metab Res       Date:  2018-04-04       Impact factor: 2.936

Review 5.  Radiological Surveillance Screening in Asymptomatic Succinate Dehydrogenase Mutation Carriers.

Authors:  Nicola Tufton; Anju Sahdev; Scott A Akker
Journal:  J Endocr Soc       Date:  2017-06-06

6.  An analysis of surveillance screening for SDHB-related disease in childhood and adolescence.

Authors:  Nicola Tufton; Lucy Shapiro; Anju Sahdev; Ajith V Kumar; Lee Martin; William M Drake; Scott A Akker; Helen L Storr
Journal:  Endocr Connect       Date:  2019-03-01       Impact factor: 3.335

Review 7.  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

Review 8.  Contemporary management of paragangliomas of the head and neck.

Authors:  Eoin F Cleere; Julie Martin-Grace; Adrien Gendre; Mark Sherlock; James P O'Neill
Journal:  Laryngoscope Investig Otolaryngol       Date:  2021-11-26

9.  Natural History and Management of Familial Paraganglioma Syndrome Type 1: Long-Term Data from a Large Family.

Authors:  Giulia Puliani; Franz Sesti; Tiziana Feola; Nicola Di Leo; Giorgia Polti; Monica Verrico; Roberta Modica; Annamaria Colao; Andrea Lenzi; Andrea M Isidori; Vito Cantisani; Elisa Giannetta; Antongiulio Faggiano
Journal:  J Clin Med       Date:  2020-02-21       Impact factor: 4.241

10.  Tumour detection and outcomes of surveillance screening in SDHB and SDHD pathogenic variant carriers.

Authors:  Gemma White; Anand Velusamy; Samantha Anandappa; Michael Masucci; Louise A Breen; Mamta Joshi; Barbara McGowan; Johnathan G H Hubbard; Rupert Obholzer; Dimitra Christodoulou; Audrey Jacques; Philip Touska; Fahim-Ul Hassan; Louise Izatt; Paul V Carroll
Journal:  Endocr Connect       Date:  2022-02-16       Impact factor: 3.335

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.