نتایج جستجو برای: CCSK

تعداد نتایج: 36  

2018
Zeynep Canan Ozdemir Burcu Ayvaci Yeter Duzenli Kar Mehmet Oguzman Mehmet Surhan Arda Mustafa Fuat Acikalin Ozcan Bor

Clear cell sarcoma of the kidney (CCSK) is an uncommon renal neoplasm of childhood. It represents between 2% and 9% of all pediatric renal tumors, and generally arises before the age of 5 years. It often mimics other pediatric renal tumors. Presently described is the case of a 7-year-old girl who presented with complaints of vomiting and abdominal pain. Abdominal ultrasonography revealed a righ...

2013
Samin Alavi Maliheh Khoddami Mohammad Kaji Yazdi Paria Dehghanian Sadaf Esteghamati

Clear cell sarcoma of the kidney (CCSK) is a rare renal neoplasm of paediatrics, making up about 3% of all renal tumours in paediatrics, with a high tendency for developing bone metastasis. A seven year-old boy was referred to our clinic with two firm, large masses over the manubrium of the sternum and right frontal area, which pathologically were confirmed as a metastatic CCSK. The patient had...

Journal: :Cancer research 1989
E Ishii J Fujimoto S Hara S Tanaka J Hata

The biological nature of human sarcomatous Wilms' tumor (SWT) was studied by analyzing newly established SWT lines, both heterotransplantable in nude mice and cultured in vitro. Five lines in nude mice include two from clear cell sarcoma of the kidney (CCSK), two from malignant rhabdoid tumor of the kidney (MRTK), and one from unclassified sarcoma. Five in vitro lines include three from CCSK, o...

2016
Jenny Karlsson Anders Valind Caroline Jansson Maureen J. O'Sullivan Linda Holmquist Mengelbier David Gisselsson

The global methylation profile and the mutational status of 633 specific epigenetic regulators were analyzed in the pediatric tumor clear cell sarcoma of the kidney (CCSK). Methylation array analyses of 30 CCSKs revealed CCSK tumor DNA to be globally hypermethylated compared to Wilms tumor, normal fetal kidney, and adult kidney. The aberrant methylation pattern of CCSKs was associated with acti...

Journal: :Journal of pediatric surgery 2011
Nidhi Sugandhi Gayatri Munghate Dhananjay P Malankar Shambhunath Das Akshya Kumar Bisoi Arun Kumar Gupta Sandeep Agarwala

Clear cell sarcoma of the kidney (CCSK) is a rare renal tumor. Only 4 cases of CCSK with vascular thrombus have been reported, and 2 of these were pediatric cases. One of the children had an intraatrial thrombus as well. We describe a 3-year-old boy who was diagnosed as having a Wilms tumor but did not respond to preresection chemotherapy. He underwent complete resection of the tumor under card...

2013
Hitomi Ueno Hajime Okita Shingo Akimoto Kenichiro Kobayashi Kazuhiko Nakabayashi Kenichiro Hata Junichiro Fujimoto Jun-ichi Hata Masahiro Fukuzawa Nobutaka Kiyokawa

A number of specific, distinct neoplastic entities occur in the pediatric kidney, including Wilms' tumor, clear cell sarcoma of the kidney (CCSK), congenital mesoblastic nephroma (CMN), rhabdoid tumor of the kidney (RTK), and the Ewing's sarcoma family of tumors (ESFT). By employing DNA methylation profiling using Illumina Infinium HumanMethylation27, we analyzed the epigenetic characteristics ...

2015
Masaya Kato Yuya Sato Keitaro Fukushima Mayuko Okuya Hidemitsu Kurosawa Shigeko Kuwashima Koichi Honma Kentaro Okamoto Takashi Tsuchioka Osamu Arisaka

A 9-year-old male presented with a renal tumor that showed a cystic structure with calcification on computed tomography. A pathological analysis of the resected tumor suggested clear cell sarcoma of the kidney (CCSK). Thus, this patient suffered atypical CCSK with significant calcification and gross necrosis. A novel chromosomal abnormality was also identified in the tumor.

2014
Shalini Sinha Nita Khurana Yogesh Kumar Sarin

Clear cell sarcoma of kidney (CCSK) is an aggressive renal neoplasm. We report two boys aged three and half, and three years with CCSK, one of whom had a disease free survival of four years and eight months. These patients were managed with surgery, chemotherapy and radiotherapy. One of the patients discontinued treatment early and lost to follow up. Aggressive multimodality therapy is the keys...

Journal: :Oncotarget 2015
Annalisa Astolfi Fraia Melchionda Daniela Perotti Maura Fois Valentina Indio Milena Urbini Chiara Giusy Genovese Paola Collini Nunzio Salfi Marilina Nantron Paolo D'Angelo Filippo Spreafico Andrea Pession

PURPOSE Clear cell sarcoma of the kidney (CCSK) is a rare pediatric renal tumor that is frequently difficult to distinguish among other childhood renal tumors due to its histological heterogeneity. This work evaluates genetic abnormalities carried by a series of CCSK samples by whole transcriptome sequencing (WTS), to identify molecular biomarkers that could improve the diagnostic process. ME...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2005
Colleen Cutcliffe Donna Kersey Chiang-Ching Huang Yong Zeng David Walterhouse Elizabeth J Perlman

PURPOSE AND EXPERIMENTAL DESIGN Clear cell sarcoma of the kidney (CCSK), the second most common renal tumor in children, poses significant diagnostic challenges. No positive diagnostic markers are available, and the pathogenesis of CCSK remains an enigma. To address these challenges, the gene expression patterns of 14 CCSKs were compared with 15 Wilms tumors and 3 fetal kidney samples using oli...

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