Garibaldi Brian, King Karen E, Jaffe Julie M, Moliterno Alison R
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Am J Hematol. 2008 Mar;83(3):242-4. doi: 10.1002/ajh.21069.
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.
温抗体型自身免疫性溶血性贫血(AIHA)是一种罕见的临床病症。它通常由针对红细胞膜的IgG自身抗体引起,主要导致脾脏内的血管外溶血。因此,导致脾功能亢进的疾病状态或手术操作预计会增加患有潜在温抗体型AIHA患者的红细胞破坏。我们报告一例先前未确诊的温抗体型AIHA患者,该患者在接受胰十二指肠切除术以切除神经内分泌肿瘤期间进行脾静脉结扎后,溶血情况恶化。