Results 281 to 290 of about 3,009,060 (331)
Some of the next articles are maybe not open access.
The American Journal of Surgery, 1965
Abstract Bilateral Wilms' tumor is rare and its treatment is not clear at the present time. In an effort to clarify treatment a patient with bilateral Wilms' tumor was presented and was compared with the four patients in the literature who were successfully treated.
H E, SNYDER +3 more
openaire +4 more sources
Abstract Bilateral Wilms' tumor is rare and its treatment is not clear at the present time. In an effort to clarify treatment a patient with bilateral Wilms' tumor was presented and was compared with the four patients in the literature who were successfully treated.
H E, SNYDER +3 more
openaire +4 more sources
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2004
AbstractWilms tumor (WT), an embryonic tumor arising from undifferentiated renal mesenchyme, has been a productive model for understanding the role of genes in both tumorigenesis and normal organogenesis. Approximately 2% of WT patients have a family history of WT, and even sporadic WT is thought to have a strong genetic component to its etiology ...
E Cristy, Ruteshouser, Vicki, Huff
openaire +2 more sources
AbstractWilms tumor (WT), an embryonic tumor arising from undifferentiated renal mesenchyme, has been a productive model for understanding the role of genes in both tumorigenesis and normal organogenesis. Approximately 2% of WT patients have a family history of WT, and even sporadic WT is thought to have a strong genetic component to its etiology ...
E Cristy, Ruteshouser, Vicki, Huff
openaire +2 more sources
Pediatric Surgery International, 1999
During a 16-year period, 49 children were treated for Wilms' tumor (WT); 7 were bilateral, 5 synchronous and 2 metachronous. The age at primary diagnosis was 6 months to 5 years (mean 2.4 years). All but 1 child received preoperative chemotherapy with tumor reduction. Unilateral nephrectomy was performed in 2 metachronous cases.
C M, Kullendorff, T, Wiebe
openaire +2 more sources
During a 16-year period, 49 children were treated for Wilms' tumor (WT); 7 were bilateral, 5 synchronous and 2 metachronous. The age at primary diagnosis was 6 months to 5 years (mean 2.4 years). All but 1 child received preoperative chemotherapy with tumor reduction. Unilateral nephrectomy was performed in 2 metachronous cases.
C M, Kullendorff, T, Wiebe
openaire +2 more sources
Journal of Pediatric Surgery, 1995
Neonatal renal tumors are very rare. We have identified 15 cases of Wilm's tumors diagnosed in the first 30 days of life. The most common presentation was an abdominal mass on routine newborn examination, and three tumors were noted on an antenatal ultrasound. All of the infants underwent primary excision of the tumor.
M L, Ritchey +4 more
openaire +2 more sources
Neonatal renal tumors are very rare. We have identified 15 cases of Wilm's tumors diagnosed in the first 30 days of life. The most common presentation was an abdominal mass on routine newborn examination, and three tumors were noted on an antenatal ultrasound. All of the infants underwent primary excision of the tumor.
M L, Ritchey +4 more
openaire +2 more sources
International Journal of Radiation Oncology*Biology*Physics, 1980
Abstract Twenty children with bilateral Wilms' tumor presented to the Children's Hospital Medical Center and Children's Cancer Research Foundation, Sidney Farber Cancer Institute, and Joint Center for Radiation Therapy (CHM-CCCRF, SFCI, JCRT) from January 1, 1956 to December 31, 1976. Of these 20, 16 had simultaneous and 4 had metachronous disease on
A W, Malcolm +3 more
openaire +2 more sources
Abstract Twenty children with bilateral Wilms' tumor presented to the Children's Hospital Medical Center and Children's Cancer Research Foundation, Sidney Farber Cancer Institute, and Joint Center for Radiation Therapy (CHM-CCCRF, SFCI, JCRT) from January 1, 1956 to December 31, 1976. Of these 20, 16 had simultaneous and 4 had metachronous disease on
A W, Malcolm +3 more
openaire +2 more sources
European Journal of Pediatric Surgery, 1993
Extrarenal nephroblastoma (Wilms' tumor) is very rare with to date just 34 cases described. Two such cases out of a total of 61 patients with WT presenting to a single institution over a 10-year period are presented. Both children, a boy aged three years and a girl aged four years, both presented with an abdominal mass which had crossed the midline ...
K, Rasheed +4 more
openaire +2 more sources
Extrarenal nephroblastoma (Wilms' tumor) is very rare with to date just 34 cases described. Two such cases out of a total of 61 patients with WT presenting to a single institution over a 10-year period are presented. Both children, a boy aged three years and a girl aged four years, both presented with an abdominal mass which had crossed the midline ...
K, Rasheed +4 more
openaire +2 more sources
Journal of Pediatric Surgery, 1966
Abstract Of 6 cases of bilateral Wilms' tumor (8.3 per cent of all cases seen in 25 years) 4 presented with bilateral involvement initially and 2 developed contralateral involvement 27 and 39 months after unilateral nephrectomy. Although one child is surviving and free of apparent disease 4 years after Actinomycin D and irradiation alone, the ...
H C, Bishop, J W, Hope
openaire +2 more sources
Abstract Of 6 cases of bilateral Wilms' tumor (8.3 per cent of all cases seen in 25 years) 4 presented with bilateral involvement initially and 2 developed contralateral involvement 27 and 39 months after unilateral nephrectomy. Although one child is surviving and free of apparent disease 4 years after Actinomycin D and irradiation alone, the ...
H C, Bishop, J W, Hope
openaire +2 more sources
The American Journal of Surgery, 1965
Summary A case of extrarenal Wilms' tumor in a three year old child is presented with a brief description of its clinical and pathologic features. The tumor was removed, and the patient treated with actinomycin D and radiotherapy.
G, EDELSTEIN +3 more
openaire +2 more sources
Summary A case of extrarenal Wilms' tumor in a three year old child is presented with a brief description of its clinical and pathologic features. The tumor was removed, and the patient treated with actinomycin D and radiotherapy.
G, EDELSTEIN +3 more
openaire +2 more sources
Brain and other central nervous system tumor statistics, 2021
Ca-A Cancer Journal for Clinicians, 2021Kimberly D Miller +2 more
exaly