Vujanić G M
Department of Paediatric Pathology, Mother and Child Health Institute, Belgrade, Serbia, Yugoslavia.
Scand J Urol Nephrol. 1992;26(3):315-7. doi: 10.3109/00365599209180892.
A 3-month-old baby boy presented with a right-sided abdominal mass that was shown on radiographic and ultrasonographic examination to be cystic and within the kidney. Histological examination of the right nephrectomy specimen showed it to be a congenital cystic mesoblastic nephroma. The patient made an uneventful recovery and there were no signs of recurrence eight years later. Though this tumour is extremely rare it should be considered as a differential diagnosis in infancy as its prognosis and treatment are different from those of other tumours.
一名3个月大的男婴因右侧腹部肿块就诊，影像学和超声检查显示肿块为囊性，位于肾脏内。右侧肾切除标本的组织学检查显示为先天性囊性中胚层肾瘤。患者恢复顺利，8年后无复发迹象。尽管这种肿瘤极为罕见，但在婴儿期应将其视为鉴别诊断之一，因为其预后和治疗与其他肿瘤不同。
