Nester Carla M, Benner Eric J, Latour Mathieu, Nickeleit Volker, Hamrick Harvey, Primack William
Department of Internal Medicine and Pediatrics, Divisions of Nephrology, The University of Iowa Hospitals and Clinics, Iowa City, IA 52242-1081, USA.
Am J Kidney Dis. 2009 May;53(5):866-70. doi: 10.1053/j.ajkd.2009.01.015. Epub 2009 Mar 20.
Cryoglobulinemia is rarely reported in children, and kidney failure secondary to cryoglobulinemia is even more uncommon. We report the case of a 7-year-old boy with cryoglobulins and a systemic illness, including persistent fever, arthralgias, rash, hypocomplementemia, and acute kidney injury associated with nephritic urine sediment. An extensive workup showed no infectious, neoplastic, or rheumatological cause of his kidney injury. The kidney biopsy specimen showed membranoproliferative glomerulonephritis type 1 with electron microscopic evidence of rhomboid crystalloid inclusions. These inclusions have rarely been reported in adult patients with cryoglobulinemia. The patient underwent spontaneous remission, including full recovery of kidney function, and required no immune suppression. The patient's course is consistent with cryoglobulinemia-associated kidney injury, which supports the inclusion of essential cryoglobulinemia in the differential diagnosis of pediatric patients with hypocomplementemic glomerulonephritis.
冷球蛋白血症在儿童中鲜有报道,继发于冷球蛋白血症的肾衰竭更为罕见。我们报告一例7岁男孩,患有冷球蛋白血症及全身性疾病,包括持续发热、关节痛、皮疹、补体低下,以及伴有肾炎性尿沉渣的急性肾损伤。全面检查未发现其肾损伤有感染、肿瘤或风湿性病因。肾活检标本显示为1型膜增生性肾小球肾炎,电镜下可见菱形晶体样包涵体。这些包涵体在成人冷球蛋白血症患者中鲜有报道。该患者实现了自发缓解,包括肾功能完全恢复,且无需免疫抑制治疗。患者的病程符合冷球蛋白血症相关肾损伤,这支持在补体低下性肾小球肾炎的儿科患者鉴别诊断中纳入原发性冷球蛋白血症。