A case of autoimmune hemolytic anemia with anti-D specificity in a 1-year-old child

Sign In

  1. Home
  2. Publications
  3. Immunohematology
  4. Publication Articles
  5. Article

Publications

Share / Export Citation / Email / Print / Text size:

Immunohematology

American National Red Cross

Subject: Medical Laboratory Technology

GET ALERTS SUBSCRIBE

ISSN: 0894-203X
eISSN: 1930-3955

DESCRIPTION

Article Metrics
0
Reader(s)
0
Visit(s)
0
Comment(s)
0
Share(s)

SEARCH WITHIN CONTENT

FIND ARTICLE

Volume / Issue / page

Archive
Volume 37 (2021)
Volume 36 (2020)
Volume 35 (2019)
Volume 34 (2018)
Volume 33 (2017)
Volume 32 (2016)
Volume 31 (2015)
Volume 30 (2014)
Volume 29 (2013)
Volume 28 (2012)
Volume 27 (2011)
Volume 26 (2010)
Volume 25 (2009)
Volume 24 (2008)
Volume 23 (2007)
Volume 22 (2006)
Volume 21 (2005)
Volume 20 (2004)
Volume 19 (2003)
Volume 18 (2002)
Volume 17 (2001)
Volume 16 (2000)
Volume 15 (1999)
Volume 14 (1998)
Volume 13 (1997)
Volume 12 (1996)
Volume 11 (1995)
Volume 10 (1994)
Volume 9 (1993)
Volume 8 (1992)
Volume 7 (1991)
Volume 6 (1990)
Volume 5 (1989)
Volume 4 (1988)
Volume 3 (1987)
Related articles

VOLUME 29 , ISSUE 1 (March 2013) > List of articles

A case of autoimmune hemolytic anemia with anti-D specificity in a 1-year-old child

Rachel S. Bercovitz / Margaret Macy / Daniel R. Ambruso

Keywords : autoimmune hemolytic anemia, pediatrics, anti-D

Citation Information : Immunohematology. Volume 29, Issue 1, Pages 15-18, DOI: https://doi.org/10.21307/immunohematology-2019-118

License : (Transfer of Copyright)

Published Online: 01-December-2019

  • ARTICLE

ARTICLE

ABSTRACT

Although antibodies to antigens in the Rh blood group system are common causes of warm autoimmune hemolytic anemia, specificity for only the D antigen is rare in autoimmune hemolysis in pediatric patients. This case reports an anti-D associated with severe hemolytic anemia (Hb = 2.1 g/dL) in a previously healthy 14-month-old child who presented with a 3-day history of low-grade fevers and vomiting. Because of his severe anemia, on admission to the hospital he was found to have altered mental status, metabolic acidosis, abnormal liver function tests, and a severe coagulopathy. He was successfully resuscitated with uncrossmatched units of group O, D– blood, and after corticosteroid therapy he had complete resolution of his anti-Dmediated hemolysis.

You don't have 'Full Text' access of this article.

Purchase Article Subscribe Journal Share