Dey Anupam
Department of Medicine, All India Institute of Medical Sciences, Bhubaneswar, Orissa, India.
J Midlife Health. 2015 Jul-Sep;6(3):132-3. doi: 10.4103/0976-7800.165596.
Autoimmune hemolytic anemia (AIHA) is a rare disease with an estimated prevalence of around 17/100,000. It is often difficult to diagnose and treat AIHA, especially in elderly. A 60-year-old female was admitted with the complaints of low grade fever, on-off for 6 months, progressive fatigue and dyspnea on exertion. She was transfused with three units of blood within these 6 months. Examination revealed pallor, edema, hemic murmur, and palpable liver. Hb was 2.9 gm%, T Bil 5.2 mg/dl, ESR 160 mm, and reticulocyte count 44.05%. Direct Coombs test was positive, anti-nuclear antibody (ANA) and Anti ds DNA were positive. A diagnosis of systemic lupus erythematosus (SLE) with AIHA was considered and patient was transfused with two units of packed red cells and put on steroid (prednisolone) at 1 mg/kg body weight daily. After 3 weeks, her Hb had increased to 10.4 gm% with gross clinical improvement.
自身免疫性溶血性贫血(AIHA)是一种罕见疾病,估计患病率约为17/10万。AIHA的诊断和治疗通常很困难,尤其是在老年人中。一名60岁女性因低热持续6个月、进行性疲劳和劳力性呼吸困难入院。在这6个月内她接受了3个单位的输血。检查发现面色苍白、水肿、血管杂音和肝脏可触及。血红蛋白为2.9克%,总胆红素5.2毫克/分升,血沉160毫米,网织红细胞计数44.05%。直接抗人球蛋白试验呈阳性,抗核抗体(ANA)和抗双链DNA呈阳性。考虑诊断为系统性红斑狼疮(SLE)合并AIHA,患者输注了2个单位的浓缩红细胞,并开始每日按1毫克/千克体重服用类固醇(泼尼松龙)。3周后,她的血红蛋白升至10.4克%,临床症状明显改善。