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Paroxysmal cold hemoglobinuria due to an IgA Donath–Landsteiner antibody
Author(s) -
Whipple Nicholas S.,
Moreau Dawn AB.,
Moulds JoAnn M.,
Hankins Jane S.,
Wang Winfred C.,
Nottage Kerri A.
Publication year - 2015
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.25591
Subject(s) - medicine , autoantibody , antibody , autoimmune hemolytic anemia , immunology , hemolytic anemia , hemoglobinuria , hemolysis
Paroxysmal cold hemoglobinuria (PCH) is an autoimmune hemolytic anemia (AIHA) characterized by the presence of a Donath–Landsteiner (D‐L) antibody. PCH occurs most commonly in young children and is associated with acute, often self‐limited hemolytic anemia. The D‐L antibody is classically a biphasic IgG anti‐P autoantibody identified by the D‐L test. Rare case reports confirm the existence of IgM D‐L antibodies. We report the case of a 2‐year‐old male diagnosed with acute AIHA and found to have PCH caused by an IgA D‐L antibody. The clinical course and treatment of this condition, which has not been reported previously, are described. Pediatr Blood Cancer © 2015 Wiley Periodicals, Inc.