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首页> 外文期刊>African journal of urology >Ask-Upmark kidney with bilateral pelvi-ureteric junction obstruction – A rare entity
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Ask-Upmark kidney with bilateral pelvi-ureteric junction obstruction – A rare entity

机译:Ask-Upmark肾伴双侧骨盆-输尿管连接处梗阻–罕见的实体

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Renal segmental hypoplasia (Ask-Upmark kidney) is a congenital disorder, first described by Eric Ask-Upmark in 1929. Habib et al. called it “segmental hypoplasia of the kidney in 1965. Ask Upmark kidney is more in females and present with hypertension or sometimes as recurrent urinary tract infections. Usually unilateral, bilaterally asymmetrical segmental hypoplasia has also been reported. The pathogenesis of Ask-Upmark kidney is controversial, attributing to vesicoureteral reflux (VUR) with intrarenal reflux or possibility of localized developmental arrest. We report a case of two years’ male child presenting as abdominal swelling with respiratory distress. On evaluation he was found to have bilateral pelvi-ureteric junction obstruction and left non-functioning kidney for which he underwent right pyeloplasty and left nephrectomy later on. Histopathology report of left kidney suggestive of segmental renal hypoplasia (Ask-Upmark kidney).
机译:肾节段发育不全(Ask-Upmark肾)是一种先天性疾病,最早由Eric Ask-Upmark于1929年描述。 1965年被称为“肾脏的节段性增生”。Ask Upmark肾脏多发于女性,并伴有高血压或有时作为尿路反复感染。通常也有单侧,双侧不对称节段性增生的报道。 Ask-Upmark肾脏的发病机制是有争议的,归因于膀胱输尿管反流(VUR)与肾内反流或局部发育停滞的可能性。我们报告了一名2岁男孩,因腹部不适而出现呼吸窘迫。经评估,他被发现患有双侧骨盆-输尿管连接阻塞和左功能不全的肾脏,随后对其进行了右肾盂成形术和左肾切除术。左肾的组织病理学报告提示节段性肾发育不全(Ask-Upmark肾)。

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