Couri Felicia Sadie, Kandula Manasa
Department of Internal Medicine, University of Illinois College of Medicine, Peoria, IL, USA.
Am J Case Rep. 2020 Feb 7;21:e920760. doi: 10.12659/AJCR.920760.
BACKGROUND Evans syndrome is characterized by 'warm' autoimmune hemolytic anemia and autoimmune thrombocytopenia, and is more common in the pediatric population than in adults. Evans syndrome is often associated with underlying autoimmune disease, connective tissue disease, immune deficiency disorders, lymphoproliferative disorders, or malignancy of the immune system. A case is presented of acute kidney injury due to hemoglobin cast nephropathy in an adult man with Evans syndrome. CASE REPORT A 60-year-old man was diagnosed with Evans syndrome, which was complicated by acute renal failure that required treatment with hemodialysis. Laboratory tests and renal histology confirmed a diagnosis of hemolysis-associated hemoglobin cast nephropathy. CONCLUSIONS The diagnosis of Evans syndrome is important as it may be associated with underlying hematological and immunological disorders. Although rare, hemoglobin cast nephropathy due to hemolysis can be a cause of acute kidney injury in patients with Evans syndrome.
伊文斯综合征的特征为“温抗体型”自身免疫性溶血性贫血和自身免疫性血小板减少症,在儿科人群中比在成人中更常见。伊文斯综合征常与潜在的自身免疫性疾病、结缔组织病、免疫缺陷病、淋巴增殖性疾病或免疫系统恶性肿瘤相关。本文报告1例患有伊文斯综合征的成年男性因血红蛋白管型肾病导致急性肾损伤的病例。病例报告:一名60岁男性被诊断为伊文斯综合征,并发急性肾衰竭,需要进行血液透析治疗。实验室检查和肾脏组织学检查确诊为溶血相关性血红蛋白管型肾病。结论:伊文斯综合征的诊断很重要,因为它可能与潜在的血液学和免疫学疾病相关。虽然罕见,但溶血导致的血红蛋白管型肾病可能是伊文斯综合征患者急性肾损伤的一个原因。