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多囊性发育不良和交叉异位肾。

Multicystic dysplasia and crossed renal ectopia.

作者信息

Nussbaum A R, Hartman D S, Whitley N, McCauley R G, Sanders R C

出版信息

AJR Am J Roentgenol. 1987 Aug;149(2):407-10. doi: 10.2214/ajr.149.2.407.

Abstract

Multicystic renal dysplasia in a crossed fused or nonfused ectopic kidney is a rare occurrence that produces unusual imaging findings. In four such cases in neonates, three presented with a palpable abdominal mass and one was discovered in utero with maternal sonography. In three cases, sonography showed a multicystic mass, contiguous with the lower pole of the orthotopic kidney. In the fourth infant, a crossed, tiny dysplastic kidney was not visualized, but its markedly dilated ectopic ureter was seen traversing the spine on CT. Ureteropelvic junction obstruction was present in the three fused orthotopic kidneys. The characteristic imaging findings of multicystic dysplasia and crossed renal ectopia include a multicystic mass of variable size that is contiguous with the lower pole of a hydronephrotic, malrotated kidney; ureteral displacement and/or dilatation; and contralateral absence of the kidney and its renal artery.

摘要

交叉融合或未融合的异位肾中多囊性肾发育不良是一种罕见情况,会产生不寻常的影像学表现。在4例新生儿此类病例中,3例表现为可触及的腹部肿块,1例在子宫内通过母体超声检查发现。3例中,超声显示一个多囊性肿块,与正位肾下极相邻。在第4例婴儿中,交叉的微小发育不良肾未显影,但在CT上可见其明显扩张的异位输尿管穿过脊柱。3例融合的正位肾存在输尿管肾盂连接处梗阻。多囊性发育不良和交叉肾异位的特征性影像学表现包括大小不一的多囊性肿块,与肾积水、旋转不良的肾脏下极相邻;输尿管移位和/或扩张;以及对侧肾脏及其肾动脉缺如。

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