Saxton H M, Golding S J, Chantler C, Haycock G D
Br J Radiol. 1981 Jul;54(643):555-61. doi: 10.1259/0007-1285-54-643-555.
Five cases of cystic dysplastic (multicystic) kidney occurring in infancy are described, in whom diagnostic puncture was used to confirm the suspected diagnosis. The characteristic finding on contrast injection was that the cystic spaces communicated via tubular structures, presumably nephronic, so ruling out the possibility of hydronephrosis. This finding also supports the view that cysts in multicystic kidney derive from nephrons and are not due to dilated calices. Although urography and ultrasonography both give appearances highly suggestive of multicystic kidney, the appearances on renal puncture are pathognomonic. When such appearances are demonstrated there is no urgent need for operative removal, except when necessitated by the size of the mass.
本文描述了5例婴儿期发生的囊性发育不良(多囊性)肾病例,其中通过诊断性穿刺来确诊疑似诊断。造影剂注射后的特征性表现是囊性间隙通过管状结构相通,推测为肾单位,从而排除了肾积水的可能性。这一发现也支持了多囊性肾囊肿起源于肾单位而非肾盂扩张的观点。尽管尿路造影和超声检查的表现都高度提示多囊性肾,但肾穿刺的表现具有诊断性。当出现这种表现时,除了肿块大小所需外,无需紧急手术切除。