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Case Report: An Atypical Case of Carney Complex
Patient: Male, 54-year-old Final Diagnosis: Carney complex (CNC) Symptoms: Cough • dyspnea • heart failure • lightheadedness • palpitation Medication: — Clinical Procedure: Mitral valve repair • open heart surgery • transesophageal echocardiogram • transthoracic echocardiogram Specialty: Cardiac Sur...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552419/ https://www.ncbi.nlm.nih.gov/pubmed/34689149 http://dx.doi.org/10.12659/AJCR.933744 |
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author | Khan, Zulqarnain Alkhatib, Hani Ramani, Gautam V. |
author_facet | Khan, Zulqarnain Alkhatib, Hani Ramani, Gautam V. |
author_sort | Khan, Zulqarnain |
collection | PubMed |
description | Patient: Male, 54-year-old Final Diagnosis: Carney complex (CNC) Symptoms: Cough • dyspnea • heart failure • lightheadedness • palpitation Medication: — Clinical Procedure: Mitral valve repair • open heart surgery • transesophageal echocardiogram • transthoracic echocardiogram Specialty: Cardiac Surgery • Cardiology • Endocrinology and Metabolic • Genetics OBJECTIVE: Rare disease BACKGROUND: Intracardiac tumors are a rare entity, with myxomas being the most common among them (approximately 50% of intracardiac tumors). Up to 80% of myxomas originate within the left atrium and while most are incidental or isolated findings in asymptomatic patients, others may result in clinical manifestations of heart failure or emboli. Moreover, in some cases, myxomas can be part of a genetically inherited syndrome known as Carney complex (CNC), and present with varied phenotypes, including skin, endocrine, and neuroendocrine tumors. CASE REPORT: We present a case of a 54-year-old male patient who presented with a several-month history of non-specific cough, dyspnea on exertion, and palpitations along with several skin tags, nevi, and nodules. He was found to have a retrocardiac density on chest X-ray, which was revealed to be a large left atrial myxoma on echocardiography. The myxoma was surgically excised and genetic testing for a mutation of the PRKAR1A gene (the most common mutation underlying CNC) was negative. However, 2 major clinical criteria for diagnosis of CNC were fulfilled based on cardiac myxoma and spotty skin pigmentation. In this report, we focus on the clinical manifestations of CNC, including guidance on tumor surveillance and genetic variants of CNC. CONCLUSIONS: While CNC is most commonly associated with an inactivating mutation of the PRKAR1A gene, it can be diagnosed clinically in the absence of an identifiable genetic mutation. In patients presenting with atypical cardiac tumors, the early recognition of cutaneous manifestations can raise the index of suspicion for CNC, which can facilitate early diagnosis, treatment, and initiation of surveillance for neoplasia development. |
format | Online Article Text |
id | pubmed-8552419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85524192021-11-10 Case Report: An Atypical Case of Carney Complex Khan, Zulqarnain Alkhatib, Hani Ramani, Gautam V. Am J Case Rep Articles Patient: Male, 54-year-old Final Diagnosis: Carney complex (CNC) Symptoms: Cough • dyspnea • heart failure • lightheadedness • palpitation Medication: — Clinical Procedure: Mitral valve repair • open heart surgery • transesophageal echocardiogram • transthoracic echocardiogram Specialty: Cardiac Surgery • Cardiology • Endocrinology and Metabolic • Genetics OBJECTIVE: Rare disease BACKGROUND: Intracardiac tumors are a rare entity, with myxomas being the most common among them (approximately 50% of intracardiac tumors). Up to 80% of myxomas originate within the left atrium and while most are incidental or isolated findings in asymptomatic patients, others may result in clinical manifestations of heart failure or emboli. Moreover, in some cases, myxomas can be part of a genetically inherited syndrome known as Carney complex (CNC), and present with varied phenotypes, including skin, endocrine, and neuroendocrine tumors. CASE REPORT: We present a case of a 54-year-old male patient who presented with a several-month history of non-specific cough, dyspnea on exertion, and palpitations along with several skin tags, nevi, and nodules. He was found to have a retrocardiac density on chest X-ray, which was revealed to be a large left atrial myxoma on echocardiography. The myxoma was surgically excised and genetic testing for a mutation of the PRKAR1A gene (the most common mutation underlying CNC) was negative. However, 2 major clinical criteria for diagnosis of CNC were fulfilled based on cardiac myxoma and spotty skin pigmentation. In this report, we focus on the clinical manifestations of CNC, including guidance on tumor surveillance and genetic variants of CNC. CONCLUSIONS: While CNC is most commonly associated with an inactivating mutation of the PRKAR1A gene, it can be diagnosed clinically in the absence of an identifiable genetic mutation. In patients presenting with atypical cardiac tumors, the early recognition of cutaneous manifestations can raise the index of suspicion for CNC, which can facilitate early diagnosis, treatment, and initiation of surveillance for neoplasia development. International Scientific Literature, Inc. 2021-10-24 /pmc/articles/PMC8552419/ /pubmed/34689149 http://dx.doi.org/10.12659/AJCR.933744 Text en © Am J Case Rep, 2021 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Khan, Zulqarnain Alkhatib, Hani Ramani, Gautam V. Case Report: An Atypical Case of Carney Complex |
title | Case Report: An Atypical Case of Carney Complex |
title_full | Case Report: An Atypical Case of Carney Complex |
title_fullStr | Case Report: An Atypical Case of Carney Complex |
title_full_unstemmed | Case Report: An Atypical Case of Carney Complex |
title_short | Case Report: An Atypical Case of Carney Complex |
title_sort | case report: an atypical case of carney complex |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552419/ https://www.ncbi.nlm.nih.gov/pubmed/34689149 http://dx.doi.org/10.12659/AJCR.933744 |
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