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Carney-Stratakis syndrome: A dyad of familial paraganglioma and gastrointestinal stromal tumor

Carney-Stratakis syndrome is a rare, distinct dyad of familial paraganglioma and gastrointestinal stromal tumor, and is associated with germline mutations in the succinate dehydrogenase genes SDHB, SDHC, and SDHD. We present a unique case of a 45-year-old woman with Carney-Stratakis syndrome who ini...

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Detalles Bibliográficos
Autores principales: Recht, Hannah S., Fishman, Elliot K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481509/
https://www.ncbi.nlm.nih.gov/pubmed/32944103
http://dx.doi.org/10.1016/j.radcr.2020.08.002
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author Recht, Hannah S.
Fishman, Elliot K.
author_facet Recht, Hannah S.
Fishman, Elliot K.
author_sort Recht, Hannah S.
collection PubMed
description Carney-Stratakis syndrome is a rare, distinct dyad of familial paraganglioma and gastrointestinal stromal tumor, and is associated with germline mutations in the succinate dehydrogenase genes SDHB, SDHC, and SDHD. We present a unique case of a 45-year-old woman with Carney-Stratakis syndrome who initially presented with a palpable left neck mass. Further workup demonstrated 2 paragangliomas in the neck and multiple SDHB deficient gastrointestinal stromal tumors of the stomach. We describe the imaging findings and clinical course of this rare syndrome.
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spelling pubmed-74815092020-09-16 Carney-Stratakis syndrome: A dyad of familial paraganglioma and gastrointestinal stromal tumor Recht, Hannah S. Fishman, Elliot K. Radiol Case Rep Case Report Carney-Stratakis syndrome is a rare, distinct dyad of familial paraganglioma and gastrointestinal stromal tumor, and is associated with germline mutations in the succinate dehydrogenase genes SDHB, SDHC, and SDHD. We present a unique case of a 45-year-old woman with Carney-Stratakis syndrome who initially presented with a palpable left neck mass. Further workup demonstrated 2 paragangliomas in the neck and multiple SDHB deficient gastrointestinal stromal tumors of the stomach. We describe the imaging findings and clinical course of this rare syndrome. Elsevier 2020-09-02 /pmc/articles/PMC7481509/ /pubmed/32944103 http://dx.doi.org/10.1016/j.radcr.2020.08.002 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Recht, Hannah S.
Fishman, Elliot K.
Carney-Stratakis syndrome: A dyad of familial paraganglioma and gastrointestinal stromal tumor
title Carney-Stratakis syndrome: A dyad of familial paraganglioma and gastrointestinal stromal tumor
title_full Carney-Stratakis syndrome: A dyad of familial paraganglioma and gastrointestinal stromal tumor
title_fullStr Carney-Stratakis syndrome: A dyad of familial paraganglioma and gastrointestinal stromal tumor
title_full_unstemmed Carney-Stratakis syndrome: A dyad of familial paraganglioma and gastrointestinal stromal tumor
title_short Carney-Stratakis syndrome: A dyad of familial paraganglioma and gastrointestinal stromal tumor
title_sort carney-stratakis syndrome: a dyad of familial paraganglioma and gastrointestinal stromal tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481509/
https://www.ncbi.nlm.nih.gov/pubmed/32944103
http://dx.doi.org/10.1016/j.radcr.2020.08.002
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