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首页> 外文期刊>Fetal and pediatric pathology >Pediatric hydronephrotic segmental renal dysplasia with ipsilateral ureterovesical obstruction--rare coincidence or a consequence?
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Pediatric hydronephrotic segmental renal dysplasia with ipsilateral ureterovesical obstruction--rare coincidence or a consequence?

机译:小儿肾积水肾节异型增生伴同侧输尿管阻塞-罕见的巧合还是后果?

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摘要

Obstruction in the developing urinary tract during embryonic life is one of the factors promoting disordered metanephric development in renal dysplasia. Dysplastic kidneys usually undergo involution during the first 5 years of life. Herein, we narrate a rare case of hydronephrotic segmental dysplasia co-existing with ipsilateral ureterovesical obstruction, in a 7-year-old male child, masquerading as hydronephrosis. Etiopathogenesis of segmental dysplasia presenting at this age is not clearly understood, and could be a consequence of intrauterine obstructive uropathy. Histologic evidence of dysplasia in a hydronephrotic kidney should warrant a close follow-up for pathologic changes in the contralateral kidney or urinary tract.
机译:胚胎生命中发育中的尿路梗阻是促进肾发育不良的后肾发展紊乱的因素之一。发育不良的肾脏通常在生命的头5年内会退行。在此,我们叙述了一个7岁男童伪装为肾积水的少见的肾积水节段性异型增生与同侧输尿管阻塞并存的情况。目前尚不清楚这一年龄段节段性增生的病因,这可能是宫内阻塞性尿毒症的结果。肾积水性肾脏发育不良的组织学证据应确保对侧肾脏或泌尿道的病理变化进行密切随访。

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