Bilateral Wilms Tumor in a Wilms Tumor Family: Case Report

1955 ◽  
Vol 73 (3) ◽  
pp. 468-474 ◽  
Author(s):  
W.L. Fitzgerald ◽  
H.C. Hardin
Keyword(s):  
Case Report ◽  
Wilms Tumor ◽  
Family Case ◽  
Bilateral Wilms Tumor

scholarly journals Renal Sparing Surgery Using Focus Ultracision Harmonic Scalpel in Patients with Bilateral Wilms’ Tumor: Case Report

2013 ◽  
Vol 30 (3) ◽  
pp. 318-320 ◽  
Author(s):  
Murat Alkan ◽  
Cemal Parlakgumus ◽  
Serdar Hilmi Iskit ◽  
Recep Tuncer ◽  
Hasan Okur ◽  
...  
Keyword(s):  
Case Report ◽  
Harmonic Scalpel ◽  
Wilms Tumor ◽  
Bilateral Wilms Tumor

Congenital Bilateral Wilms Tumor: A Case Report

Urology ◽  
2021 ◽  
Author(s):  
Deguang Meng ◽  
Xiaofeng Chang ◽  
Qinghua Ren ◽  
Jiatong Xu ◽  
Huanmin Wang
Keyword(s):  
Case Report ◽  
Wilms Tumor ◽  
Bilateral Wilms Tumor

Early Detection of Wilms' Tumor in a Child with Hemihypertnophy and Ovarian Cysts

PEDIATRICS ◽  
1982 ◽  
Vol 70 (1) ◽  
pp. 135-136
Author(s):  
Deborah Tolchin ◽  
Mordecai Koenigsberg ◽  
Maria Santorineou
Keyword(s):  
Case Report ◽  
Early Detection ◽  
Ovarian Cyst ◽  
Wilms Tumor ◽  
Present Report ◽  
Ovarian Cysts ◽  
Term Pregnancy ◽  
Intravenous Pyelogram ◽  
Routine Examination ◽  
Bilateral Wilms Tumor

There have been many reports of the association between hemihypertrophy and intraabdominal masses, including Wilms' tumor, hepatoma, and adrenal cortical neoplasias.1 The present report describes a patient with segmental hemihypertrophy, multiple ovarian cysts, and bilateral Wilms' tumor and suggests a screening regimen for patients with hemihypertrophy. CASE REPORT The patient was a 9 lb 14 oz product of a term pregnancy, who was well until a mass filling the entire right side of the abdomen was discovered on routine examination at 4 months of age. Intravenous pyelogram (IVP) confirmed a large prerenal mass which on ultrasound was felt to be an ovarian cyst.

Minimally Invasive Approach for Wilms Tumor Treatment in a Small Child - A Case Report

Urology ◽  
2020 ◽  
Author(s):  
Alexandre Azevedo Ziomkowski ◽  
João Rafael Silva Simões Estrela ◽  
Nilo Jorge Carvalho Leão Barretto ◽  
Nilo César Leão Barretto
Keyword(s):  
Case Report ◽  
Minimally Invasive ◽  
Wilms Tumor ◽  
Small Child ◽  
Tumor Treatment ◽  
Minimally Invasive Approach ◽  
Invasive Approach

Myotonic dystrophy Rossolimo-Churchman-Steinert-Batten (clinical case)

2020 ◽  
pp. 71-72
Author(s):  
И.А. Синельникова ◽  
И.В. Сопрунова ◽  
О.П. Николаева
Keyword(s):  
Case Report ◽  
Myotonic Dystrophy ◽  
Clinical Case ◽  
Molecular Genetic ◽  
Ctg Repeats ◽  
Molecular Genetic Method ◽  
Genetic Method ◽  
Family Case ◽  
Dmpk Gene

В статье представлено описание семейного случая миотонической дистрофии Россолимо-Штейнерта-Куршмана-Баттена. Диагноз подтвержден в результате ДНК-диагностики: выявлено увеличенное число копий CTG-повтора гена DMPK, ответственного за развитие миотонической дистрофии. A family case report of Rossolimo-Steinert-Curschmann myotonic dystrophy is presented. An increased number of copies of CTG-repeats of the DMPK gene responsible for the development of MD, i.e., the diagnosis was confirmed by molecular genetic method.

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.

Bilateral Wilms Tumor

1987 ◽  
Vol 138 (4 Part 2) ◽  
pp. 968-973 ◽  
Author(s):  
M.L. Blute ◽  
P.P. Kelalis ◽  
K.P. Offord ◽  
N. Breslow ◽  
J.B. Beckwith ◽  
...  
Keyword(s):  
Wilms Tumor ◽  
Bilateral Wilms Tumor

scholarly journals Identification of proteins associated with pediatric bilateral Wilms tumor

2016 ◽  
Vol 12 (6) ◽  
pp. 5075-5079
Author(s):  
Zechen Yan ◽  
Qingjun Meng ◽  
Jinjian Yang ◽  
Junjie Zhang ◽  
Wei Zhao ◽  
...  
Keyword(s):  
Wilms Tumor ◽  
Bilateral Wilms Tumor

scholarly journals Malignant Rhabdoid Tumor of the Lung in the Young Adult: A Case Report

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Adel Attia ◽  
Moosa Suleman ◽  
Hesham Mosleh
Keyword(s):  
Case Report ◽  
Young Adult ◽  
Pediatric Oncology ◽  
Wilms Tumor ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor

Malignant rhabdoid tumor (MRT) is one of the most aggressive and lethal malignancies in pediatric oncology. Malignant rhabdoid tumor was initially described in 1978 as a rhabdomyosarcomatoid variant of a Wilms tumor because of its occurrence in the kidney and because of the resemblance of its cells to rhabdomyoblasts. The absence of muscular differentiation led Haas and colleagues to coin the term rhabdoid tumor of the kidney in 1981, Haas et al..

scholarly journals A Family Case Report ofSchistosoma haematobiumInfection in Italian Travelers

1995 ◽  
Vol 2 (3) ◽  
pp. 193-195 ◽  
Author(s):  
Annibale Raglio ◽  
Maurizio Parea ◽  
Vailati Francesca ◽  
Antonio Goglio
Keyword(s):  
Case Report ◽  
Family Case
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