نتایج جستجو برای: sarcomatoid carcinoma

تعداد نتایج: 394721  

2016
Jongmin Hwang Yong Hyun Park Kyung Un Choi Jeong Su Kim Ki Won Hwang Sang Hyun Lee Min Ku Chon Soo Yong Lee Dae Sung Lee

Cardiac metastasis from renal cell carcinoma (RCC) without inferior vena cava (IVC) involvements is extremely rare with few reported cases. Sarcomatoid RCC with rhabdoid feature is a rare pathologic type of RCC having aggressive behavior due to great metastatic potential. Here, we report a case of rapidly growing cardiac metastasis of RCC which brought on right ventricular outflow tract (RVOT) ...

2013
Si-Yuan Huang Shu-Jing Shen Xing-Ya Li

BACKGROUND Pulmonary sarcomatoid carcinoma is a diagnostically challenging group of tumors. It's a rare histologic subtype of non-small cell lung cancer.There are five subgroups of pulmonary sarcomatoid carcinoma, they are identified as pleomorphic carcinoma, spindle cell carcinoma, giant cell carcinoma, carcinosarcoma, and pulmonary blastoma. We explored the clinicopathologic features and prog...

2015
Chun-Hsien Chen Wei-Ming Chen Shui-Yi Tung Cheng-Shyong Wu Wei-Lin Tong Kam-Fai Lee Kuo-Liang Wei

Gastrointestinal metastases in lung cancer are extremely rare. The report presents a rare case of primary lung sarcomatoid carcinoma with both gastric and colonic metastases, and reviews the literature about endoscopic presentation of colonic metastases.

2013
Xiao-yong Shen Zhi-feng Lin Qiang Lin Zhen Ruan Hai-long Huang Chao-qiang Ju Jin Wang

Sarcomatoid carcinoma (SC) is a rare primary malignant tumor in which both carcinomatous and sarcomatous elements occur. It can occur in many different organs and anatomical locations, such as the skin, thyroid gland, bone, urinary tract, breast, pancreas, liver and other areas. Of them, pulmonary sarcomatoid carcinoma (PSC) is a rare malignant cancer composed of sarcoma and sarcoma-like tumors...

2015
Yong Fu Zobeida Cruz-Monserrate H. Helen Lin Yiyin Chung Baoan Ji Szu-min Lin Steven Vonderfecht Craig D. Logsdon Chien-Feng Li David K. Ann

Salivary duct carcinoma (SDC) is an uncommon, but aggressive malignant tumor with a high mortality rate. Herein, we reported the detection of somatic KRAS A146T and Q61H mutations in 2 out of 4 (50%) sarcomatoid SDC variants. Transgenic mice carrying the human oncogenic KRAS(G12V), which spatiotemporal activation by tamoxifen (TAM)-inducible Cre recombinase Ela-CreERT in the submandibular gland...

2017
Song Xu Xia Liu Renwang Liu Tao Shi Xiongfei Li Diansheng Zhong Yan Wang Gang Chen Jun Chen

Almost all epidermal growth factor receptor (EGFR)-mutant lung cancers develop resistance to EGFR-tyrosine kinase inhibitors. Several mechanisms for this acquired resistance have been identified, including development of an EGFR T790M mutation, MET amplification, hepatocyte growth factor overexpression, loss of phosphatase and tensin homolog expression, epithelial-mesenchymal transition, and tr...

2017
Junji Takiguchi Hirokazu Sakamoto Nobutaka Inoue

2013
Niraj Badhiwala Robert Chan Hai-Jun Zhou Steven Shen Michael Coburn

A 57-year-old man who presented with urinary retention was found to have a sarcomatoid carcinoma of the urethra. Evaluation with CT scan of the abdomen and pelvis revealed multiple pulmonary nodules and osteolytic lesions of left posterior ribs. After external beam radiation therapy and six cycles of systemic chemotherapy, patient underwent a surgical resection of the urethral cancer. After his...

2010
Kusuma Venkatesh Monika Lamba Saini S. R. Niveditha Chaithra Krishnagiri Sudarshan Babu

Primary leiomyosarcoma of the kidney is a rare tumor with an aggressive behaviour. A 55-year-old woman presented with a left sided abdominal mass in our outpatient department. Radiologic investigations revealed the mass to be renal in origin with colonic adhesions for which radical nephrectomy and hemicolectomy were done. The tumor completely appeared to replace the left kidney and had a whorle...

Journal: :Journal of cancer research and therapeutics 2008
Milind Kumar Shikha Goyal Amit Bahl Prasenjit Das D N Sharma Ruma Ray G K Rath

Sarcomatoid carcinomas are rare tumors. These tumors have been reported at other sites, but head and neck origin is extremely uncommon. We report here a rare case of sarcomatoid carcinoma involving the maxilla. Only four such cases with maxillary origin have been discussed in English literature earlier. As compared to squamous cell carcinoma of maxilla, this variant is associated with poor prog...

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