Rikitake Junpei, Kakiuchi Seiji, Takagi Ikumi, Kagebayashi Mari, Tomida Kodo, Yoshida Toshiko, Hara Shigeo, Iwata Nobuko, Kamesaki Toyomi
Department of Hematology, Yodogawa Christian Hospital.
Department of Nephrology, Yodogawa Christian Hospital.
Rinsho Ketsueki. 2023;64(2):91-96. doi: 10.11406/rinketsu.64.91.
A 62-year-old male patient was admitted for close monitoring of anemia (hemoglobin level, 8.2 g/dl). Hemolytic anemia was observed; however, the direct antiglobulin test (DAT) result (standard tube method) was negative. Nevertheless, autoimmune hemolytic anemia (AIHA) was still suspected; therefore, a DAT (Colum method) and quantifying levels of red-blood-cell bound immunoglobulin G were performed, resulting in a definite diagnosis of warm AIHA. The patient also had an acute kidney injury (AKI) from the time of admission, which was poorly improved by supplemental fluids therapy alone. Therefore, renal biopsy was performed. Renal biopsy revealed acute tubular injury due to hemoglobin columns, and a diagnosed AKI caused by hemolysis due to AIHA. Following the definitive diagnosis of AIHA, the patient was treated with prednisolone, and after approximately 2 weeks, the anemia and nephropathy completely improved, which is maintained to this day. We report this case as a rare case of AKI induced by hemolysis of AIHA and a successful case of renal salvage by early administration of steroid.
一名62岁男性患者因密切监测贫血(血红蛋白水平为8.2 g/dl)入院。观察到溶血性贫血;然而,直接抗球蛋白试验(DAT,标准试管法)结果为阴性。尽管如此,仍怀疑为自身免疫性溶血性贫血(AIHA);因此,进行了DAT(柱法)并对红细胞结合免疫球蛋白G水平进行定量,最终确诊为温抗体型AIHA。患者自入院时起还患有急性肾损伤(AKI),仅通过补充液体治疗改善不佳。因此,进行了肾活检。肾活检显示因血红蛋白柱导致急性肾小管损伤,诊断为AIHA溶血所致的AKI。在明确诊断AIHA后,患者接受泼尼松龙治疗,约2周后,贫血和肾病完全改善,至今保持良好。我们将此病例报告为AIHA溶血诱发AKI的罕见病例以及早期给予类固醇成功挽救肾脏的病例。