Cargando…

Palpitations as a presenting feature of multisystem sarcoidosis

Introduction: Sarcoidosis is described as a systemic condition characterized by non-caseating granulomas in multiple organs. In this report, we present an unusual manifestation of cardiac sarcoidosis and review management strategies. Case presentation: A 29-year-old African-American man presented wi...

Descripción completa

Detalles Bibliográficos
Autores principales: Manikat, Richie, Gilson, Julieta, Krishnamurthy, Mahesh, Khalighi, Koroush
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538218/
https://www.ncbi.nlm.nih.gov/pubmed/28808515
http://dx.doi.org/10.1080/20009666.2017.1333879
_version_ 1783254321861754880
author Manikat, Richie
Gilson, Julieta
Krishnamurthy, Mahesh
Khalighi, Koroush
author_facet Manikat, Richie
Gilson, Julieta
Krishnamurthy, Mahesh
Khalighi, Koroush
author_sort Manikat, Richie
collection PubMed
description Introduction: Sarcoidosis is described as a systemic condition characterized by non-caseating granulomas in multiple organs. In this report, we present an unusual manifestation of cardiac sarcoidosis and review management strategies. Case presentation: A 29-year-old African-American man presented with weight loss, fatigue, dyspnea, palpitations, night sweats, painless left eye redness and bilateral leg pain over the course of three months. His physical exam revealed left conjunctival congestion and bilateral crackles on auscultation. Computerized tomography of the chest showed severe parenchymal disease with bilateral fibrotic bands. Bronchoscopy and transbronchial biopsy revealed noncaseating granulomas and multinucleated giant cells, confirming sarcoidosis. Non-sustained ventricular tachycardia developed. Cardiac MRI showed myocardial delayed gadolinium enhancement. He responded to methotrexate and steroid therapy. An implantable cardioverter-defibrillator was placed. Discussion: Although cardiac sarcoidosis manifests in only 5% of sarcoidosis, autopsy reports indicate subclinical cardiac involvement in up to 30%. There are no established criteria for diagnosis of cardiac sarcoidosis. Conclusion: Early recognition and diagnosis of cardiac sarcoidosis is challenging but vital due to unpredictability and high risk for malignant cardiac involvement. Newer diagnostic imaging modalities have further aided in earlier identification and prevention of sudden cardiac death.
format Online
Article
Text
id pubmed-5538218
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-55382182017-08-14 Palpitations as a presenting feature of multisystem sarcoidosis Manikat, Richie Gilson, Julieta Krishnamurthy, Mahesh Khalighi, Koroush J Community Hosp Intern Med Perspect Case Reports Introduction: Sarcoidosis is described as a systemic condition characterized by non-caseating granulomas in multiple organs. In this report, we present an unusual manifestation of cardiac sarcoidosis and review management strategies. Case presentation: A 29-year-old African-American man presented with weight loss, fatigue, dyspnea, palpitations, night sweats, painless left eye redness and bilateral leg pain over the course of three months. His physical exam revealed left conjunctival congestion and bilateral crackles on auscultation. Computerized tomography of the chest showed severe parenchymal disease with bilateral fibrotic bands. Bronchoscopy and transbronchial biopsy revealed noncaseating granulomas and multinucleated giant cells, confirming sarcoidosis. Non-sustained ventricular tachycardia developed. Cardiac MRI showed myocardial delayed gadolinium enhancement. He responded to methotrexate and steroid therapy. An implantable cardioverter-defibrillator was placed. Discussion: Although cardiac sarcoidosis manifests in only 5% of sarcoidosis, autopsy reports indicate subclinical cardiac involvement in up to 30%. There are no established criteria for diagnosis of cardiac sarcoidosis. Conclusion: Early recognition and diagnosis of cardiac sarcoidosis is challenging but vital due to unpredictability and high risk for malignant cardiac involvement. Newer diagnostic imaging modalities have further aided in earlier identification and prevention of sudden cardiac death. Taylor & Francis 2017-07-13 /pmc/articles/PMC5538218/ /pubmed/28808515 http://dx.doi.org/10.1080/20009666.2017.1333879 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Manikat, Richie
Gilson, Julieta
Krishnamurthy, Mahesh
Khalighi, Koroush
Palpitations as a presenting feature of multisystem sarcoidosis
title Palpitations as a presenting feature of multisystem sarcoidosis
title_full Palpitations as a presenting feature of multisystem sarcoidosis
title_fullStr Palpitations as a presenting feature of multisystem sarcoidosis
title_full_unstemmed Palpitations as a presenting feature of multisystem sarcoidosis
title_short Palpitations as a presenting feature of multisystem sarcoidosis
title_sort palpitations as a presenting feature of multisystem sarcoidosis
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538218/
https://www.ncbi.nlm.nih.gov/pubmed/28808515
http://dx.doi.org/10.1080/20009666.2017.1333879
work_keys_str_mv AT manikatrichie palpitationsasapresentingfeatureofmultisystemsarcoidosis
AT gilsonjulieta palpitationsasapresentingfeatureofmultisystemsarcoidosis
AT krishnamurthymahesh palpitationsasapresentingfeatureofmultisystemsarcoidosis
AT khalighikoroush palpitationsasapresentingfeatureofmultisystemsarcoidosis