IgA nephropathy associated with Crohn disease

被引:21
作者
Dabadie, A
Gie, S
Taque, S
Babut, JM
Roussey, M
机构
来源
ARCHIVES DE PEDIATRIE | 1996年 / 3卷 / 09期
关键词
Crohn's disease; glomerulonephritis; IgA; child;
D O I
10.1016/0929-693X(96)87579-8
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background.- Renal disease is an unfrequent extraintestinal manifestation of c Case report.- A 12 year-old girl suffered from recurrent abdominal pain, diarrhea and growth impairment due to Crohn's disease of ileocaecal region. After sir months of nutritional rehabilitation, an ileo-caecal resection was performed because of intestinal stenosis. The surgical procedure was followed by parietal abcess and cutaneous fistula. One year later a purulent secretion came out off the fistula associated with fever, hematuria and acute renal failure. Renal biopsy confirmed IgA nephropathy. The course was favorable under parenteral nutrition and after surgical closure of the sigmoido-cutaneous fistula. The microscopic hematuria only persisted but the nephropathy did not relapse even during a further digestive exacerbation. Conclusion.- IgA nephropathy has been reported in association with chronic inflammatory bowel disease. Its mechanism remains unclear: increased mucosal IgA production in inflammatory bowel, increased serum IgA and/or immune complex deposition in the renal mesangium appear the most relevant hypotheses.
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页码:884 / 887
页数:4
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