Agranulocytosis in systemic lupus erythematosus: A case report

Agranulocytosis is a rare acute condition characterized by severe a < gft (neutropenia in which the neutrophils count is less than 100/mm(3). It can be classified into two categories, inherited, and acquired. Acquired agranulocytosis is not commonly caused by auto‐immune diseases such as systemic...

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Autores principales: Frikha, Olfa, Ben Salah, Raida, Mefteh, Ansar, Frikha, Faten, Snoussi, Mouna, Marzouk, Sameh, Bahloul, Zouhir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664526/
https://www.ncbi.nlm.nih.gov/pubmed/36397857
http://dx.doi.org/10.1002/ccr3.6511
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author Frikha, Olfa
Ben Salah, Raida
Mefteh, Ansar
Frikha, Faten
Snoussi, Mouna
Marzouk, Sameh
Bahloul, Zouhir
author_facet Frikha, Olfa
Ben Salah, Raida
Mefteh, Ansar
Frikha, Faten
Snoussi, Mouna
Marzouk, Sameh
Bahloul, Zouhir
author_sort Frikha, Olfa
collection PubMed
description Agranulocytosis is a rare acute condition characterized by severe a < gft (neutropenia in which the neutrophils count is less than 100/mm(3). It can be classified into two categories, inherited, and acquired. Acquired agranulocytosis is not commonly caused by auto‐immune diseases such as systemic lupus erythematosus (SLE). We report a case of a patient suffering from agranulocytosis related to SLE at disease onset, associated with other rare disease involvements.
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spelling pubmed-96645262022-11-16 Agranulocytosis in systemic lupus erythematosus: A case report Frikha, Olfa Ben Salah, Raida Mefteh, Ansar Frikha, Faten Snoussi, Mouna Marzouk, Sameh Bahloul, Zouhir Clin Case Rep Case Report Agranulocytosis is a rare acute condition characterized by severe a < gft (neutropenia in which the neutrophils count is less than 100/mm(3). It can be classified into two categories, inherited, and acquired. Acquired agranulocytosis is not commonly caused by auto‐immune diseases such as systemic lupus erythematosus (SLE). We report a case of a patient suffering from agranulocytosis related to SLE at disease onset, associated with other rare disease involvements. John Wiley and Sons Inc. 2022-11-15 /pmc/articles/PMC9664526/ /pubmed/36397857 http://dx.doi.org/10.1002/ccr3.6511 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Frikha, Olfa
Ben Salah, Raida
Mefteh, Ansar
Frikha, Faten
Snoussi, Mouna
Marzouk, Sameh
Bahloul, Zouhir
Agranulocytosis in systemic lupus erythematosus: A case report
title Agranulocytosis in systemic lupus erythematosus: A case report
title_full Agranulocytosis in systemic lupus erythematosus: A case report
title_fullStr Agranulocytosis in systemic lupus erythematosus: A case report
title_full_unstemmed Agranulocytosis in systemic lupus erythematosus: A case report
title_short Agranulocytosis in systemic lupus erythematosus: A case report
title_sort agranulocytosis in systemic lupus erythematosus: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664526/
https://www.ncbi.nlm.nih.gov/pubmed/36397857
http://dx.doi.org/10.1002/ccr3.6511
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