Horm Metab Res 2019; 51(07): 414-418
DOI: 10.1055/a-0586-3710
Review

Diagnostic Investigation of Lesions Associated with Succinate Dehydrogenase Defects

David Taïeb
1   Department of Nuclear Medicine, La Timone University Hospital, CERIMED, Aix-Marseille University, Marseille, France
,
Henri Timmers
2   Department of Internal Medicine, Division of Endocrinology, Radboud University Medical Centre, Nijmegen, The Netherlands
,
Karel Pacak
3   Section on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA
› Institutsangaben

Abstract

The mitochondrial enzyme succinate dehydrogenase (SDH) acts as a tumor suppressor. Biallelic inactivation of one of the genes encoding for SDH subunits (collectively named SDHx) leads to complete loss of the protein function and the development of diverse group of tumors. Pheochromocytomas-paragangliomas are the prime example of hereditary tumors caused by SDH deficiency. In this review, we discuss the roles of imaging examinations, and illustrate new insights into genotype-imaging phenotype relationships.



Publikationsverlauf

Eingereicht: 05. November 2017

Angenommen: 28. Februar 2018

Artikel online veröffentlicht:
04. April 2018

Georg Thieme Verlag
Rüdigerstraße 14,70469 Stuttgart, Germany

 
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