نتایج جستجو برای: small renal cell carcinoma

تعداد نتایج: 2664039  

2009
Juan Carlos Regueiro Lopez Jesus Ruiz Garcia Manuel Leva Vallejo Antonio Lopez Beltran Juan Carlos Regueiro López

OBJECTIVE: We describe a new case of incidental renal papillary carcinoma. We perform a bibliogra-phic review. METHODS: The papillary renal cell carcinoma is a variant of renal carcinoma. They classify in two subtypes that have relation with their prognosis. We presented one case of re-nal papillary carcinoma in a male of 76 years, play-acting as severe hydronephrosis. RESULTS/DISCUSSION: We de...

Journal: :Clinical imaging 2004
Giorgio Ascenti Carmela Visalli Antonino Genitori Antonio Certo Alessia Pitrone Silvio Mazziotti

Pancreatic metastases are rare. Melanoma, lung cancer and breast carcinoma are the most common origin of pancreatic metastases, whereas renal cell carcinoma is counted in only 1-2%. Renal cell carcinoma usually leads to a solitary pancreatic metastasis, whereas multiple pancreatic metastases are uncommon. We present three cases of multiple hypervascular pancreatic metastases from renal cell car...

Journal: :Proceedings 2015
Varsha Podduturi Charles J Yourshaw Haiying Zhang

Chromophobe renal cell carcinoma is a distinct subtype of renal cell carcinoma that accounts for 5% of all renal tumors. This subtype is further subdivided into two variants, classic and eosinophilic, with the latter variant being less frequent. We report two cases of the eosinophilic variant of chromophobe renal cell carcinoma diagnosed at our institution between January 2008 and December 2012.

2014
XIUJUN ZHANG FEN HU LIJUN MENG LIXIA GOU MENGMENG LUO

Transmembrane protein 174 (TMEM174) mRNA is easily detectable in human kidney tissues and activates AP-1 and promotes 293T cell proliferation. In the present study, RNA in situ hybridization was used to detect TMEM174 gene expression in various malignant renal cancer and normal renal tissues. The results showed that TMEM174 exhibits differential expression in renal tissues, with a high positive...

Journal: :Human pathology 2014
Enrico Munari Luigi Marchionni Apurva Chitre Masamichi Hayashi Guido Martignoni Matteo Brunelli Stefano Gobbo Pedram Argani Mohamad Allaf Mohammad O Hoque George J Netto

Clear cell papillary renal cell carcinoma (CCPRCC) is a low-grade renal neoplasm with morphological characteristics mimicking both clear cell renal cell carcinoma (CCRCC) and papillary renal cell carcinoma (PRCC). However, despite some overlapping features, their morphological, immunohistochemical, and molecular profiles are distinct. Micro-RNAs (miRNAs) are small noncoding RNAs that play a cru...

Journal: :American Journal of Roentgenology 1980

2014
Yu-Yi Chan Shin-Hun Juang Guan-Jhong Huang Yu-Ren Liao Yu-Fon Chen Chia-Che Wu Hui-Ting Chang Tian-Shung Wu

Phytochemical investigation of the heartwood of Michelia compressa afforded forty-four compounds, which were identified by comparison of experimental and literature analytical and spectroscopic data. Some compounds were evaluated for their anti-inflammatory and anticancer bioactivities. The result showed that soemerine (1) and cyathisterol (2) exhibited significant nitric oxide (NO) inhibition,...

Journal: :Hinyokika kiyo. Acta urologica Japonica 2006
Yuji Kato Atsushi Numata Naoki Wada Tatsuya Iwata Yuji Saga Hiroshi Hashimoto Hidehiro Kakizaki

A 52-year-old woman had a pathological fracture of the right femur. On histopathological examination bone metastasis from renal cell carcinoma was suspected. Abdominal computed tomography showed a heterogeneous mass (9.1 x 7.8 x 6.5 cm) in the left kidney and a cystic multilocular mass (12 x 10 cm) in the pelvis. Bone scintigraphy revealed an abnormal uptake in the left coracoid process, right ...

2014
Patrick R Benusiglio Sophie Giraud Sophie Deveaux Arnaud Méjean Jean-Michel Correas Dominique Joly Marc-Olivier Timsit Sophie Ferlicot Virginie Verkarre Caroline Abadie Dominique Chauveau Dominique Leroux Marie-Françoise Avril Jean-François Cordier Stéphane Richard

BACKGROUND The Birt-Hogg-Dubé syndrome is a rare cancer susceptibility syndrome characterised by renal tumours, lung cysts and pneumothoraces, and fibrofolliculomas. It is caused by dominantly inherited mutations in FLCN. Our objective was to report renal tumour characteristics in a large series of patients with the Birt-Hogg-Dubé syndrome. METHODS We studied French Birt-Hogg-Dubé patients wi...

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