نتایج جستجو برای: intravascular extension of wilms tumor

تعداد نتایج: 21220822  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Mazen A Ghanem Theo H Van der Kwast Mondastri K Sudaryo Rejiv B Mathoera Marry M van den Heuvel Abdel-Alim M Al-Doray Rien M Nijman Gert J van Steenbrugge

PURPOSE A number of studies have indicated that the tumor proliferation marker MIB-1 and cell cycle inhibitor p27(Kip1) expression are of prognostic importance in a variety of cancers. The present study was performed to evaluate the prognostic value of these molecules in Wilms' tumors. EXPERIMENTAL DESIGN MIB-1 and p27(Kip1) expressions were investigated by the means of immunohistochemical an...

2009
A. Adil Esen C. Cem Güler Ziya Kirkali

A 64-year-old man underwent left radical nephrectomy for stage III anaplastic Wilms’ tumor. He received adjuvant chemotherapy consisting of cisplatin and etoposide. Complete clinical response was achieved and maintained for 12 months. A systemic relapse after 1 year also responded to three more cycles of cisplatin and etoposide. Although cisplatinand etoposide-based chemotherapy was not used as...

Journal: :Academic Pathology 2018

Journal: :Journal of Pediatric Surgery 2019

Journal: :Sao Paulo Medical Journal 1994

2009
Kylie M. Drake E. Cristy Ruteshouser Rachael Natrajan Phyllis Harbor Jenny Wegert Manfred Gessler Kathy Pritchard-Jones Paul Grundy Jeffrey Dome Vicki Huff Chris Jones Micheala A. Aldred

Purpose: Wilms' tumor is a childhood cancer of the kidney with an incidence of ∼1 in 10,000. Cooccurrence of Wilms' tumor with 2q37 deletion syndrome, an uncommon constitutional chromosome abnormality, has been reported previously in three children. Given these are independently rare clinical entities, we hypothesized that 2q37 harbors a tumor suppressor gene important in Wilms' tumor pathogene...

2008
Ana Maria Rabelo de Carvalho Luciana Resende Bandeira de Melo Vera Lúcia Moraes Rejane Pereira Neves

Fungal infections are increasingly being reported in immuno-compromised patients. In this study we report a case of systemic Trichosporon cutaneum infection in an infant with Wilms' tumor. This is the first time that an invasive infection for T. cutaneum has been reported in a Wilms' tumor patient.

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