Fatal warm autoimmune hemolytic anemia in a child due to IgM‐type autoantibodies. Issue 8 (8th June 2016)

• Record Type: Journal Article
• Authors: Takahashi, Hiroyuki; Tanaka, Fumiko; Sakuma, Hiroyuki; Sato, Mutsumi; Inaba, Shoichi; Kai, Sumio
• Is Part Of: Pediatrics international. Volume 58:Issue 8(2016)
• Page Start: 744
• Page End: 746
• Publication Date: 2016-06-08
• Subjects: autoagglutinin -- autoimmune hemolytic anemia -- encephalopathy -- immunoglobulin M -- warm antibody; Pediatrics -- Periodicals; 618.92
• DOI: 10.1111/ped.12931
• Languages: English
• ISSNs: 1328-8067

Abstract

Abstract: Herein is described a case of immunoglobulin M (IgM) warm autoimmune hemolytic anemia (AIHA) in a child who consequently died within 3 days of clinical onset. A previously healthy 11‐year‐old boy presented with fever, anemia, jaundice, and deteriorating consciousness. On direct agglutination test against group O red blood cells, agglutination was seen even at 37°C in saline, which was abolished on dithiothreitol treatment of the serum, indicating that the responsible autoantibody was IgM and had a warm‐reactive capacity. A diagnosis of IgM warm AIHA was therefore made. Hemagglutination in the visceral capillaries was considered as the direct cause of organ dysfunction. The patient died due to respiratory failure. IgM warm AIHA is a very severe condition that is difficult to reverse in an advanced state. Both prompt, definite diagnosis and intervention are therefore vital to prevent severe multi‐organ dysfunction in cases of IgM warm AIHA.