Abstract
Warm autoimmune hemolytic anemia (AIHA) is a rare clinical entity. It is usually caused by an IgG autoantibody directed against the red blood cell membrane that causes extravascular hemolysis predominantly in the spleen. As a result, disease states or procedures that result in hypersplenism would be expected to increase red cell destruction in patients with an underlying warm AIHA. We present the case of a patient with a previously undiagnosed warm AIHA, who developed worsening hemolysis after undergoing splenic vein ligation during a pancreaticoduodenectomy to remove a neuroendocrine tumor.
Original language | English (US) |
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Pages (from-to) | 242-244 |
Number of pages | 3 |
Journal | American Journal of Hematology |
Volume | 83 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2008 |
ASJC Scopus subject areas
- Hematology