Scientific article
English

Severe autoimmune hemolytic anemia in a liver transplanted child

Published in

Pediatric transplantation, vol. 12, no. 7, p. 809-812

Publication date

2008

Abstract

AIHA can complicate solid organ and bone marrow transplantation early after transplant. We describe the first case report of a 16-month-old boy with mixed type warm-acting IgM and warm IgG autoantibodies AIHA, occurring eight months after liver transplantation. This case describes the complexity of this very rare form of AIHA. It also illustrates the efficacy of rituximab in this indication, as well as the transfusion support with extremely rare blood, along with the importance of international collaboration to provide it. In this report, the etiologies of HA occurring in post-transplant pediatric patients are reviewed and the different treatment strategies are discussed.

Keywords

  • Anemia, Hemolytic, Autoimmune/complications/etiology
  • Antibodies, Monoclonal/administration & dosage/chemistry
  • Autoantibodies/chemistry
  • Blood Transfusion
  • Child
  • Humans
  • Immunoglobulin G/chemistry
  • Immunoglobulin M/chemistry
  • Immunologic Factors/administration & dosage
  • Infant
  • Liver Diseases/complications
  • Liver Transplantation/adverse effects/methods
  • Male

Citation (ISO format)

SCHAEPPI, Michela et al. Severe autoimmune hemolytic anemia in a liver transplanted child. In: Pediatric transplantation, 2008, vol. 12, n° 7, p. 809–812. doi: 10.1111/j.1399-3046.2008.00934.x

Main files (1)

Article (Accepted version)

Identifiers

Journal ISSN

1397-3142
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Technical informations

Creation

20/05/2009 16:02:00

First validation

20/05/2009 16:02:00

Update

14/03/2023 15:05:21

Status update

14/03/2023 15:05:21

Last indexation

29/10/2024 11:34:57
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