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肾母细胞瘤,或称Wilms瘤,是一种胚胎性肿瘤,该肿瘤为儿童实体恶性肿瘤最常见的一种,约占5～10%,其中40%以上为双侧性.病因学上,肾母细胞瘤可分为遗传性和非遗传性二大类.前者包括所有双侧性和部分单侧生病例;后者仅包括单侧性病例.本文报道了一例具有3;17易位的双侧肾母细胞瘤.患儿、男性、23个月,因血尿及腹围增大就医,无先天畸形或肾脏疾病家族史.体
Nephroblastoma, or Wilms’s tumor, is an embryonal tumor that is the most common form of childhood solid malignancy, accounting for approximately 5-10%, of which more than 40% is bilateral. Etiologically, Nephroblastoma can be divided into two categories: hereditary and non-hereditary. The former includes all bilateral and partial unilateral cases; the latter includes only unilateral cases. This article reports a case with a 3;17 translocation. Bilateral nephroblastoma. Child, male, 23 months, hematuria and abdominal circumference increased medical treatment, no congenital malformation or family history of kidney disease.