Yun Seongseok, Walker Courtney N, Vincelette Nicole D, Anwer Faiz
Department of Internal Medicine, University of Arizona Medical Center, Tucson, Arizona, USA.
College of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
BMJ Case Rep. 2014 Jun 9;2014:bcr2014205044. doi: 10.1136/bcr-2014-205044.
We describe a rare case of a 19-year-old male patient with a history of epilepsy and developmental delay who presented with acute renal failure (ARF) and lactic acidosis (LA) as the first manifestation of T-cell lymphoblastic lymphoma. Renal ultrasound and CT of the abdomen showed renal parenchymal infiltration, and renal biopsy demonstrated T-cell lymphoblastic lymphoma. LA, ARF and electrolyte abnormalities were refractory to the initial treatment of bicarbonate infusion and hydration. However, these abnormalities rapidly normalised after the initiation of chemotherapy, suggesting that the LA and ARF were secondary to lymphomatous renal infiltration.
我们描述了一例罕见病例,一名19岁男性患者,有癫痫和发育迟缓病史,以急性肾衰竭(ARF)和乳酸性酸中毒(LA)作为T细胞淋巴母细胞淋巴瘤的首发表现。肾脏超声和腹部CT显示肾实质浸润,肾活检证实为T细胞淋巴母细胞淋巴瘤。乳酸酸中毒、急性肾衰竭和电解质异常对初始的碳酸氢盐输注和补液治疗无效。然而,化疗开始后这些异常迅速恢复正常,提示乳酸酸中毒和急性肾衰竭是淋巴瘤肾脏浸润的继发表现。