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Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report

Acquired angioedema (AAE) is a rare disease with life-threatening complications. This pathology has classically been associated with medication use and B cell lymphoproliferative disorders. In this report, we describe a 61-year-old man with a six-year history of angioedema, unrelated to any known tr...

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Detalles Bibliográficos
Autores principales: Kochvar, Andrew P, Cobb, Gavin, Bernabe, Celina C, Levine, Terry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510307/
https://www.ncbi.nlm.nih.gov/pubmed/37736455
http://dx.doi.org/10.7759/cureus.43841
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author Kochvar, Andrew P
Cobb, Gavin
Bernabe, Celina C
Levine, Terry
author_facet Kochvar, Andrew P
Cobb, Gavin
Bernabe, Celina C
Levine, Terry
author_sort Kochvar, Andrew P
collection PubMed
description Acquired angioedema (AAE) is a rare disease with life-threatening complications. This pathology has classically been associated with medication use and B cell lymphoproliferative disorders. In this report, we describe a 61-year-old man with a six-year history of angioedema, unrelated to any known triggers or malignancy. Extensive workup has led to a diagnosis of idiopathic nonhistaminergic AAE with normal C1 inhibitor. The patient is currently being treated with lanadelumab, which has resolved the patient’s symptoms. This case provides insight into the onset, exploration, treatment, and outcomes of an extremely rare disease process.
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spelling pubmed-105103072023-09-21 Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report Kochvar, Andrew P Cobb, Gavin Bernabe, Celina C Levine, Terry Cureus Allergy/Immunology Acquired angioedema (AAE) is a rare disease with life-threatening complications. This pathology has classically been associated with medication use and B cell lymphoproliferative disorders. In this report, we describe a 61-year-old man with a six-year history of angioedema, unrelated to any known triggers or malignancy. Extensive workup has led to a diagnosis of idiopathic nonhistaminergic AAE with normal C1 inhibitor. The patient is currently being treated with lanadelumab, which has resolved the patient’s symptoms. This case provides insight into the onset, exploration, treatment, and outcomes of an extremely rare disease process. Cureus 2023-08-21 /pmc/articles/PMC10510307/ /pubmed/37736455 http://dx.doi.org/10.7759/cureus.43841 Text en Copyright © 2023, Kochvar 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 Allergy/Immunology
Kochvar, Andrew P
Cobb, Gavin
Bernabe, Celina C
Levine, Terry
Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report
title Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report
title_full Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report
title_fullStr Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report
title_full_unstemmed Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report
title_short Acquired Non-histaminergic Angioedema With C1q Autoantibody and Urticaria: A Case Report
title_sort acquired non-histaminergic angioedema with c1q autoantibody and urticaria: a case report
topic Allergy/Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510307/
https://www.ncbi.nlm.nih.gov/pubmed/37736455
http://dx.doi.org/10.7759/cureus.43841
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