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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Detalles Bibliográficos
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
Descripción
Sumario: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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