[川崎病急性肾功能不全]。

Archives francaises de pediatrie Pub Date : 1993-06-01
C Sevin, L Heidet, M F Gagnadoux, G Chéron, P Niaudet
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引用次数: 0

摘要

背景:川崎病是一种急性炎症性疾病,以多种特征的组合为特征,但累及肾脏是罕见的。本文报告一例川崎病并发急性肾衰竭。病例报告:一名十岁女童因急性肾功能衰竭伴发热入院。她发高烧,全身状况很差;10天前,她出现了黄斑红斑疹,并给予头孢地洛辛治疗。入院时,患者发热,有草莓舌、咽炎、唇干红斑、双侧结膜炎、颈淋巴肿大、手部皮肤脱屑。她贫血(血红蛋白= 9.6 g%),白细胞增多(33,100/mm3),但无毛刺,红细胞碎片化或血小板减少。血浆c反应蛋白236 mg/l;血尿素9.5 mmol/l,肌酐288 mmol/l,蛋白尿0.5 g/l,无血尿。尿液培养没有增长。她的血液转氨酶和γ -谷氨酰转移酶活性升高。肾脏及冠状动脉超声检查正常。入院后1天肾活检未见血管或肾小球改变,但肾小管坏死,提示尿中色素排泄。肌红蛋白血症、肌红蛋白尿和血肌酶活性检测均呈阳性。肾衰在10天内消失,但发热和炎症症状持续1 1/2-2个月,尽管静脉注射了γ球蛋白和持续给药水杨酸。患者在发病第一个月末出现关节痛,但恢复后无肾脏或血管并发症。结论:在川崎病的病程中,报告了几例肾脏受累的病例。组织学检查很少有文献记载,因此血管起源的改变尚未得到证实。肌红蛋白尿,见于肌肉挤压伤,在我们的病例中可能是由于恶性高热,可能是造成短暂性急性肾功能衰竭的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Acute renal insufficiency in Kawasaki disease].

Background: Kawasaki disease is an acute inflammatory condition characterized by various combinations of features but renal involvement is rare. This report is of a case of Kawasaki disease complicated by acute kidney failure.

Case report: A 10 year-old girl was admitted because of acute renal failure with fever. She developed a high fever, and her general condition was poor; she had developed a macular erythematous rash 10 days earlier for which she was given cefadroxil. At admission, she remained febrile and had strawberry tongue, pharyngitis, dry erythematous lips, bilateral conjunctivitis, cervical lymphadenopathy and desquamation of the skin on her hands. She was anemic (hemoglobin = 9.6 g%), leukocytotic (33,100/mm3), but with no burr, fragmented red blood cells or thrombocytopenia. Her plasma C-reactive protein level was 236 mg/l; her blood urea was 9.5 mmol/l, her creatininemia 288 mumol/l and proteinuria was 0.5 g/l without hematuria. Urine cultures did not grow. Her blood transaminase and gammaglutamyltransferase activities were elevated. Ultrasonography of kidneys and coronary arteries was normal. Kidney biopsy performed one day after admission showed no vascular or glomerular changes, but renal tubular necrosis, indicating urinary excretion of pigments. Tests for myoglobinemia, myoglobinuria and blood muscle enzyme activities were all positive. The renal failure disappeared within 10 days but the fever and inflammatory manifestations persisted for 1 1/2-2 months despite two treatments of intravenous gammaglobulins and continuous salicylate administration. The patient developed arthralgias at the end of the first month of disease, but recovered without renal or vascular complications.

Conclusions: Several cases of renal involvement have been reported during the course of Kawasaki disease. They have been rarely documented by histological examination so that the vascular origin of changes has not been demonstrated. Myoglobinuria, as seen in muscular crush injury, and in our case possibly due to malignant hyperthermia, may be responsible for the transient acute renal failure.

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