Abstract
Management of functional intrathoracic sympathetic paragangliomas in succinate dehydrogenase subunit D (SDHD) mutation carriers is challenging, and there is no uniform guideline for treatment to date. The risks of potential malignant behavior and long-term cardiovascular morbidity have to be weighed against the risks of treatment complications. We report the multidisciplinary and shared decision-making approach that resulted in successful surgical removal of 3 paragangliomas in a SDHD mutation carrier.
Copyright © 2020 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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DNA Mutational Analysis
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DNA, Neoplasm / genetics*
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Head and Neck Neoplasms / diagnosis
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Head and Neck Neoplasms / genetics*
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Head and Neck Neoplasms / metabolism
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Humans
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Magnetic Resonance Imaging
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Male
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Mutation*
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Neoplasms, Multiple Primary / diagnosis
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Neoplasms, Multiple Primary / genetics*
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Neoplasms, Multiple Primary / metabolism
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Neoplastic Syndromes, Hereditary / diagnosis
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Neoplastic Syndromes, Hereditary / genetics
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Neoplastic Syndromes, Hereditary / metabolism
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Paraganglioma / diagnosis
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Paraganglioma / genetics
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Paraganglioma / metabolism
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Positron Emission Tomography Computed Tomography
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Succinate Dehydrogenase / genetics*
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Succinate Dehydrogenase / metabolism
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Thoracic Neoplasms / diagnosis
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Thoracic Neoplasms / genetics*
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Thoracic Neoplasms / metabolism
Substances
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DNA, Neoplasm
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SDHD protein, human
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Succinate Dehydrogenase