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Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency

BACKGROUND: We describe the first case of a patient with factitious disorder who closely simulated a primary immune deficiency disorder – Common Variable Immune Deficiency (CVID), by surreptitiously ingesting non-steroidal anti-inflammatory agents. CASE DESCRIPTION: He was treated with several expen...

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Autores principales: Ameratunga, Rohan, Casey, Paul, Parry, Susan, Kenedi, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848570/
https://www.ncbi.nlm.nih.gov/pubmed/24341706
http://dx.doi.org/10.1186/1710-1492-9-36
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author Ameratunga, Rohan
Casey, Paul
Parry, Susan
Kenedi, Chris
author_facet Ameratunga, Rohan
Casey, Paul
Parry, Susan
Kenedi, Chris
author_sort Ameratunga, Rohan
collection PubMed
description BACKGROUND: We describe the first case of a patient with factitious disorder who closely simulated a primary immune deficiency disorder – Common Variable Immune Deficiency (CVID), by surreptitiously ingesting non-steroidal anti-inflammatory agents. CASE DESCRIPTION: He was treated with several expensive and potentially dangerous drugs before the diagnosis was established through collateral information. In retrospect he did not meet the proposed new criteria for CVID. These criteria may prove useful in distinguishing cases of CVID from secondary hypogammaglobulinemia. CONCLUSION: It is imperative clinicians recognise patients with factitious disorder at the earliest opportunity to prevent iatrogenic morbidity and mortality.
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spelling pubmed-38485702013-12-04 Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency Ameratunga, Rohan Casey, Paul Parry, Susan Kenedi, Chris Allergy Asthma Clin Immunol Case Report BACKGROUND: We describe the first case of a patient with factitious disorder who closely simulated a primary immune deficiency disorder – Common Variable Immune Deficiency (CVID), by surreptitiously ingesting non-steroidal anti-inflammatory agents. CASE DESCRIPTION: He was treated with several expensive and potentially dangerous drugs before the diagnosis was established through collateral information. In retrospect he did not meet the proposed new criteria for CVID. These criteria may prove useful in distinguishing cases of CVID from secondary hypogammaglobulinemia. CONCLUSION: It is imperative clinicians recognise patients with factitious disorder at the earliest opportunity to prevent iatrogenic morbidity and mortality. BioMed Central 2013-09-17 /pmc/articles/PMC3848570/ /pubmed/24341706 http://dx.doi.org/10.1186/1710-1492-9-36 Text en Copyright © 2013 Ameratunga et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ameratunga, Rohan
Casey, Paul
Parry, Susan
Kenedi, Chris
Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency
title Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency
title_full Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency
title_fullStr Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency
title_full_unstemmed Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency
title_short Hypogammaglobulinemia factitia- Munchausen syndrome masquerading as common variable immune deficiency
title_sort hypogammaglobulinemia factitia- munchausen syndrome masquerading as common variable immune deficiency
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3848570/
https://www.ncbi.nlm.nih.gov/pubmed/24341706
http://dx.doi.org/10.1186/1710-1492-9-36
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