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An Unusual Presentation of Cogan’s Syndrome With a Renal Tumor: A Report of a Rare Case

Cogan’s syndrome (CS) is a rare disorder of an unknown origin characterized by inflammatory eye disease and vestibuloauditory symptoms, primarily affecting young white adults, without a hereditary pattern. The exclusion of other diseases makes diagnosis difficult, and it is likely underreported in t...

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Detalles Bibliográficos
Autores principales: Kirsch, John P, Nottoli, Madeline M, Findakly, Dawood, Wang, Jue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436999/
https://www.ncbi.nlm.nih.gov/pubmed/37602005
http://dx.doi.org/10.7759/cureus.42123
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author Kirsch, John P
Nottoli, Madeline M
Findakly, Dawood
Wang, Jue
author_facet Kirsch, John P
Nottoli, Madeline M
Findakly, Dawood
Wang, Jue
author_sort Kirsch, John P
collection PubMed
description Cogan’s syndrome (CS) is a rare disorder of an unknown origin characterized by inflammatory eye disease and vestibuloauditory symptoms, primarily affecting young white adults, without a hereditary pattern. The exclusion of other diseases makes diagnosis difficult, and it is likely underreported in the literature. A 74-year-old previously healthy African American male presented with ear and jaw pain, later accompanied by vestibular symptoms, fever of unknown origin, aortitis, and a third-degree heart block. The workup revealed incidental renal cell carcinoma and interstitial keratitis. This case highlights the challenge of diagnosing an atypical presentation of CS with late-onset interstitial keratitis by excluding other complex syndromes.
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spelling pubmed-104369992023-08-19 An Unusual Presentation of Cogan’s Syndrome With a Renal Tumor: A Report of a Rare Case Kirsch, John P Nottoli, Madeline M Findakly, Dawood Wang, Jue Cureus Internal Medicine Cogan’s syndrome (CS) is a rare disorder of an unknown origin characterized by inflammatory eye disease and vestibuloauditory symptoms, primarily affecting young white adults, without a hereditary pattern. The exclusion of other diseases makes diagnosis difficult, and it is likely underreported in the literature. A 74-year-old previously healthy African American male presented with ear and jaw pain, later accompanied by vestibular symptoms, fever of unknown origin, aortitis, and a third-degree heart block. The workup revealed incidental renal cell carcinoma and interstitial keratitis. This case highlights the challenge of diagnosing an atypical presentation of CS with late-onset interstitial keratitis by excluding other complex syndromes. Cureus 2023-07-19 /pmc/articles/PMC10436999/ /pubmed/37602005 http://dx.doi.org/10.7759/cureus.42123 Text en Copyright © 2023, Kirsch et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Kirsch, John P
Nottoli, Madeline M
Findakly, Dawood
Wang, Jue
An Unusual Presentation of Cogan’s Syndrome With a Renal Tumor: A Report of a Rare Case
title An Unusual Presentation of Cogan’s Syndrome With a Renal Tumor: A Report of a Rare Case
title_full An Unusual Presentation of Cogan’s Syndrome With a Renal Tumor: A Report of a Rare Case
title_fullStr An Unusual Presentation of Cogan’s Syndrome With a Renal Tumor: A Report of a Rare Case
title_full_unstemmed An Unusual Presentation of Cogan’s Syndrome With a Renal Tumor: A Report of a Rare Case
title_short An Unusual Presentation of Cogan’s Syndrome With a Renal Tumor: A Report of a Rare Case
title_sort unusual presentation of cogan’s syndrome with a renal tumor: a report of a rare case
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436999/
https://www.ncbi.nlm.nih.gov/pubmed/37602005
http://dx.doi.org/10.7759/cureus.42123
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