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Unusual presentation of familial Mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis

Acute post‐streptococcal glomerulonephritis (APSGN) and polyarteritis nodosa (PAN) may occur simultaneously after streptococcal infection in a child who is previously healthy but carries a Mediterranean fever (MEFV) mutation. The homozygous M694V mutation in the MEFV gene may cause an augmented resp...

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Autores principales: Özdemir Atikel, Yeşim, Derinkuyu, Betül Emine, Bakkaloğlu, Sevcan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307881/
https://www.ncbi.nlm.nih.gov/pubmed/35898740
http://dx.doi.org/10.1002/ccr3.6022
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author Özdemir Atikel, Yeşim
Derinkuyu, Betül Emine
Bakkaloğlu, Sevcan A.
author_facet Özdemir Atikel, Yeşim
Derinkuyu, Betül Emine
Bakkaloğlu, Sevcan A.
author_sort Özdemir Atikel, Yeşim
collection PubMed
description Acute post‐streptococcal glomerulonephritis (APSGN) and polyarteritis nodosa (PAN) may occur simultaneously after streptococcal infection in a child who is previously healthy but carries a Mediterranean fever (MEFV) mutation. The homozygous M694V mutation in the MEFV gene may cause an augmented response to the streptococcal infection that plays a role in the development of both clinical manifestations.
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spelling pubmed-93078812022-07-26 Unusual presentation of familial Mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis Özdemir Atikel, Yeşim Derinkuyu, Betül Emine Bakkaloğlu, Sevcan A. Clin Case Rep Case Report Acute post‐streptococcal glomerulonephritis (APSGN) and polyarteritis nodosa (PAN) may occur simultaneously after streptococcal infection in a child who is previously healthy but carries a Mediterranean fever (MEFV) mutation. The homozygous M694V mutation in the MEFV gene may cause an augmented response to the streptococcal infection that plays a role in the development of both clinical manifestations. John Wiley and Sons Inc. 2022-07-22 /pmc/articles/PMC9307881/ /pubmed/35898740 http://dx.doi.org/10.1002/ccr3.6022 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Özdemir Atikel, Yeşim
Derinkuyu, Betül Emine
Bakkaloğlu, Sevcan A.
Unusual presentation of familial Mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis
title Unusual presentation of familial Mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis
title_full Unusual presentation of familial Mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis
title_fullStr Unusual presentation of familial Mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis
title_full_unstemmed Unusual presentation of familial Mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis
title_short Unusual presentation of familial Mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis
title_sort unusual presentation of familial mediterranean fever with co‐existing polyarteritis nodosa and acute post‐streptococcal glomerulonephritis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307881/
https://www.ncbi.nlm.nih.gov/pubmed/35898740
http://dx.doi.org/10.1002/ccr3.6022
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