Aplasia eritroide aguda y amegacariocitosis por el lupus eritematoso sistémico

Background - Anemia and thrombocytopenia are common features in patients with systemic lupus erythematosus (SLE). However, erythroid aplasia and amegakaryocytosis as the main physiopathological causes without other associated disorders have been rarely described. Case report – We report of a 29...

詳細記述

書誌詳細
出版年:Galicia Clínica
主要な著者: Rui Suzano, Juvenal Morais, José Fernandes, Judite Sachicumbi, Luis Caminal-Montero
フォーマット: 論文
言語:英語
出版事項: Sociedade Galega de Medicina Interna 2023-09-01
主題:
オンライン・アクセス:https://galiciaclinica.info/publicacion.asp?f=2910
その他の書誌記述
要約:Background - Anemia and thrombocytopenia are common features in patients with systemic lupus erythematosus (SLE). However, erythroid aplasia and amegakaryocytosis as the main physiopathological causes without other associated disorders have been rarely described. Case report – We report of a 29 y/o female with diagnosis of SLE presenting with severe anemia and thrombocytopenia due to a bone marrow immunological blockage. Patient, who initially refused transfusions, was successfully treated and had a very fast hematological response to steroids, immunoglobulin, plasma exchange, eltrombopag and rituximab. Discussion– This is an unusual case and it is possible that in this kind of patients plasma exchange associated with immunosuppressant therapy may lead to a faster, more effective and sustained recovery of the hematological disorders.
ISSN:0304-4866
1989-3922