Nephroblastomatosis and Wilms tumour: report of 2 cases.

被引：0

作者：

Jouini, R ^{[1
]}

Maazoun, K ^{[1
]}

Chelly, S ^{[1
]}

Mekki, M ^{[1
]}

Belgnith, M ^{[1
]}

Nouri, A ^{[1
]}

机构：

[1] Hop Univ Fattouma Bourguiba, Serv Chirurg Pediat, Monastir 5000, Tunisia

来源：

PROGRES EN UROLOGIE | 2003年 / 13卷 / 02期

关键词：

Wilms tumour; nephroblastomatosis; child;

D O I：

暂无

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Nephroblastomatosis is a rare disease, considered to be a precursor of Wilms tumour When it is isolated, recommended treatment consists of chemotherapy followed by surveillance. In the presence of associated Wilms tumour treatment consists of preoperative chemotherapy followed by partial nephrectomy (when possible), followed by postoperative chemotherapy and surveillance.

引用

页码：273 / 276

页数：4

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