Extrarenal Wilms tumor: a case report and review of the literature

2013 ◽  
Vol 48 (6) ◽  
pp. e33-e35 ◽  
Author(s):  
Yesenia Rojas ◽  
Bethany J. Slater ◽  
Richard M. Braverman ◽  
Karen W. Eldin ◽  
Patrick A. Thompson ◽  
...  
Keyword(s):  
Case Report ◽  
Wilms Tumor ◽  
Review Of The Literature

scholarly journals Is it always Wilms’ tumor? Localized cystic disease of the kidney in an infant. An extremely rare case report and review of the literature

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Christos Kaselas ◽  
Charikleia Demiri ◽  
Vasilios Mouravas ◽  
Eleni Koutra ◽  
Kleanthis Anastasiadis ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Wilms Tumor ◽  
Pediatric Population ◽  
Benign Disease ◽  
Cystic Disease ◽  
Proper Treatment ◽  
Review Of The Literature ◽  
Rare Case Report ◽  
Renal Malignancies

Localized Cystic Disease of the Kidney (LCDK) is an extremely rare benign disease in pediatric population. Although its management is conservative and generally requires no treatment, the unfamiliarity with the disease can expose such patients to misdiagnosis as renal malignancies or uncertainty for proper treatment. We report such a case in an infant and review the current literature.

Wilms' Tumor of the Cervix: A Case Report and Review of the Literature

2000 ◽  
Vol 76 (1) ◽  
pp. 107-111 ◽  
Author(s):  
Elizabeth A. Babin ◽  
John R. Davis ◽  
Kenneth D. Hatch ◽  
Alton V. Hallum
Keyword(s):  
Case Report ◽  
Wilms Tumor ◽  
Review Of The Literature

Adult Wilms Tumor in the Renal Pelvis: Case Report With Review of the Literature

Urology ◽  
2008 ◽  
Vol 72 (5) ◽  
pp. 1185.e5-1185.e7
Author(s):  
Kosuke Okasho ◽  
Hiroyuki Nishiyama ◽  
Jun Watanabe ◽  
Takeshi Soda ◽  
Yoshiki Mikami ◽  
...  
Keyword(s):  
Case Report ◽  
Renal Pelvis ◽  
Wilms Tumor ◽  
Review Of The Literature

scholarly journals Fetal rhabdomyomatous nephroblastoma -a variant of Wilms tumor: A case report and review of the literature

2017 ◽  
Vol 4 (5) ◽  
pp. 364-368
Author(s):  
Pedraza Bermeo ◽  
Adriana Marcela ◽  
Ortiz Zableh ◽  
Ana Maria ◽  
Pérez Niño ◽  
...  
Keyword(s):  
Case Report ◽  
Wilms Tumor ◽  
Review Of The Literature

scholarly journals Composite tumor of metanephric adenoma and Wilms’ tumor of the kidney: A case report and review of the literature

2013 ◽  
Vol 5 (4) ◽  
pp. 1311-1314 ◽  
Author(s):  
PENGCHENG ZHU ◽  
FEI YAN ◽  
ZIXUAN YANG ◽  
LI MENG ◽  
QILIN AO
Keyword(s):  
Case Report ◽  
Wilms Tumor ◽  
Review Of The Literature ◽  
Metanephric Adenoma ◽  
Composite Tumor

scholarly journals Botryoid Wilms’ tumor: a case report and review of the literature

2013 ◽  
Vol 11 (1) ◽  
pp. 102 ◽  
Author(s):  
Guofeng Xu ◽  
Jimeng Hu ◽  
Yeming Wu ◽  
Yongtao Xiao ◽  
Maosheng Xu
Keyword(s):  
Case Report ◽  
Wilms Tumor ◽  
Review Of The Literature

Primary extrarenal Wilms' tumor in the inguinal canal: Case report and review of the literature

1996 ◽  
Vol 31 (7) ◽  
pp. 957-959 ◽  
Author(s):  
Marc S Arkovitz ◽  
Howard B Ginsburg ◽  
Josef Eidelman ◽  
M.Alba Greco ◽  
Aaron Rauson
Keyword(s):  
Case Report ◽  
Wilms Tumor ◽  
Inguinal Canal ◽  
Review Of The Literature

Association of Wilms tumor in multicystic dysplastic kidneys: case report and review of the literature

2021 ◽  
pp. 205141582110240
Author(s):  
Darian Andreas ◽  
Richard D Glick ◽  
Jonathan D Fish ◽  
Carolyn Fein Levy ◽  
Jordan S Gitlin
Keyword(s):  
Case Report ◽  
Antenatal Diagnosis ◽  
Wilms Tumor ◽  
Multicystic Dysplastic Kidney ◽  
Review Of The Literature ◽  
Level Of Evidence ◽  
Renal Anomalies ◽  
Dysplastic Kidney ◽  
Increased Risk ◽  
Dysplastic Kidneys

Multicystic dysplastic kidney is a rare urinary anomaly characterized by multiple non-communicating cysts resulting in a non-functional kidney. In addition to association with hypertension and contralateral renal anomalies, children with multicystic dysplastic kidney have an increased risk of Wilms tumor. Cohort studies and systematic reviews are hampered in estimating the true risk of this association due to the rarity and infrequent reporting of the condition. We present a case of a 2-year-old male child with an antenatal diagnosis of multicystic dysplastic kidney undergoing surveillance ultrasonography who presented with a symptomatic Wilms tumor. Level of evidence: Not applicable for this multicentre audit.

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