Literature DB >> 26892457

Systemic lupus erythematosus presenting with mixed-type fulminant autoimmune hemolytic anemia.

Yoko Hirano1, Takaaki Itonaga1, Hiroki Yasudo1, Tsuyoshi Isojima1, Kenichiro Miura1, Yutaka Harita1, Masahiro Sekiguchi1, Motohiro Kato1, Junko Takita1, Akira Oka1.   

Abstract

We report the case of a 9-year-old girl who presented with mixed-type fulminant autoimmune hemolytic anemia (AIHA) at the onset of systemic lupus erythematosus (SLE). On admission, laboratory investigations indicated very severe anemia (Hb, 2.7 g/dL) with reticulocytosis and positive direct/indirect Coombs tests. In addition, agglutinative reaction was clinically observed. Based on further examinations, the patient was diagnosed with AIHA complicated with SLE, and mixed-type AIHA was clinically identified. With oral prednisolone and methylprednisolone pulse therapy, the patient entered remission.
© 2016 Japan Pediatric Society.

Entities:  

Keywords:  Coombs test; children; mixed-type autoimmune hemolytic anemia; reticulocytosis; systemic lupus erythematosus

Year:  2016        PMID: 26892457     DOI: 10.1111/ped.12849

Source DB:  PubMed          Journal:  Pediatr Int        ISSN: 1328-8067            Impact factor:   1.524


  1 in total

1.  Irregular antibodies in no hemolytic autoimmune diseases are able to induce erythrophagocytosis.

Authors:  Paola Ester López-Díaz; María Del Rocío Ruiz-Olivera; Luis Alberto Hernández-Osorio; Jaime Vargas-Arzola; Xareni Valle-Jiménez; Sergio Roberto Aguilar-Ruiz; Honorio Torres-Aguilar
Journal:  Immunol Res       Date:  2017-02       Impact factor: 2.829

  1 in total

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