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Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene

Paragangliomas (PGLs) are rare neural tumors that can be benign or malignant and often associated with familial syndromes. We present a case of a 23-year-old male with a large retroperitoneal PGL found incidentally during the workup of elevated liver enzymes. After surgical excision, the patient was...

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Autores principales: Chen, Wen Min, Olson, Philip, Arcot, Rohith, Nguyen, Huy, Quereshi, Faisal, Kokenakes, Courtney, Cher, Michael L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Codon Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842840/
https://www.ncbi.nlm.nih.gov/pubmed/33564614
http://dx.doi.org/10.15586/jkcvhl.v8i1.129
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author Chen, Wen Min
Olson, Philip
Arcot, Rohith
Nguyen, Huy
Quereshi, Faisal
Kokenakes, Courtney
Cher, Michael L.
author_facet Chen, Wen Min
Olson, Philip
Arcot, Rohith
Nguyen, Huy
Quereshi, Faisal
Kokenakes, Courtney
Cher, Michael L.
author_sort Chen, Wen Min
collection PubMed
description Paragangliomas (PGLs) are rare neural tumors that can be benign or malignant and often associated with familial syndromes. We present a case of a 23-year-old male with a large retroperitoneal PGL found incidentally during the workup of elevated liver enzymes. After surgical excision, the patient was found to have an autosomal dominant mutation in the succinate dehydrogenase B (SDHB) gene, which when compared to sporadic PGLs or other familial syndromes is associated with a higher risk of tumor recurrence, occult metastasis, and development of other cancers. The patient’s first-degree relatives were recommended to undergo screening for the genetic mutation.
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spelling pubmed-78428402021-02-08 Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene Chen, Wen Min Olson, Philip Arcot, Rohith Nguyen, Huy Quereshi, Faisal Kokenakes, Courtney Cher, Michael L. J Kidney Cancer VHL Pheochromocytoma Paragangliomas (PGLs) are rare neural tumors that can be benign or malignant and often associated with familial syndromes. We present a case of a 23-year-old male with a large retroperitoneal PGL found incidentally during the workup of elevated liver enzymes. After surgical excision, the patient was found to have an autosomal dominant mutation in the succinate dehydrogenase B (SDHB) gene, which when compared to sporadic PGLs or other familial syndromes is associated with a higher risk of tumor recurrence, occult metastasis, and development of other cancers. The patient’s first-degree relatives were recommended to undergo screening for the genetic mutation. Codon Publications 2021-01-25 /pmc/articles/PMC7842840/ /pubmed/33564614 http://dx.doi.org/10.15586/jkcvhl.v8i1.129 Text en Copyright: Chen W M et al. http://creativecommons.org/licenses/by/4.0/ This open access article is licensed under Creative Commons Attribution 4.0 International (CC BY 4.0). http://creativecommons.org/licenses/by/4.0
spellingShingle Pheochromocytoma
Chen, Wen Min
Olson, Philip
Arcot, Rohith
Nguyen, Huy
Quereshi, Faisal
Kokenakes, Courtney
Cher, Michael L.
Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene
title Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene
title_full Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene
title_fullStr Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene
title_full_unstemmed Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene
title_short Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene
title_sort large retroperitoneal paraganglioma associated with germline mutation of the succinate dehydrogenase gene
topic Pheochromocytoma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842840/
https://www.ncbi.nlm.nih.gov/pubmed/33564614
http://dx.doi.org/10.15586/jkcvhl.v8i1.129
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