نتایج جستجو برای: malignant rhabdoid tumor

تعداد نتایج: 564247  

Journal: :Cancer research 1990
R Handgretinger A Kimmig E Koscielnak D Schmidt G Rudolph H Wolburg W Paulus K Schilbach-Stueckle C Ottenlinger A Menrad

A new human cell line (Wa-2) derived from an extrarenal rhabdoid tumor has been established. The cell line grows as a monolayer consisting of round- and spindle-shaped cells. Injection of cells into nude mice results in the growth of solid tumors within 2 wk of inoculation. These solid tumors have the microscopic appearance similar to that of the original tumor from which the cell line was deri...

2016
Max Seiter Motasem Al Maaieh Andrew Rosenberg Sheila Conway

Primary osteosarcoma of the bone with rhabdoid features is a rare malignant tumor of bone, not previously described in the literature. Here we report a 69-year-old female who originally presented with a right femur pathologic fracture. Radiographs of the injury showed an aggressive-appearing lesion of the distal femur. Initial biopsy was done, which was not diagnostic; additional advanced imagi...

Journal: :Sarcoma 2007
Ryan Horazdovsky J. Carlos Manivel Edward Y. Cheng

Purpose. The objective of this study is to report a case of a rare, highly lethal tumor, extrarenal malignant rhabdoid tumor (EMRT) in a 43-year-old man who initially presented with a local recurrence and is now continuously disease free 14 years after aggressive surgical treatment. The case and literature are discussed.

Journal: :journal of research in medical sciences 0
santosh kumar mondal palash kumar mandal anindya adhikari bijan basak

primary sarcoma of the breast is very rare and constitutes less than 1% of all breast cancers. herein, we report a case of pleomorphic rhabdomyosarcoma (prms) of the right breast in a 49-year-old female patient presented with a mass (7 cm × 6.5 cm). mammography and ultrasonography suspected a malignant lesion and a diagnosis of poorly differentiated carcinoma was made on fine needle aspiration ...

2014
Bhaskar Kahali Jinlong Yu Stefanie B. Marquez Kenneth. W. Thompson Shermi Y. Liang Li Lu David Reisman

Rhabdoid sarcomas are highly malignant tumors that usually occur in young children. A key to the genesis of this tumor is the mutational loss of the BAF47 gene as well as the widespread epigenetic suppression of other key anticancer genes. The BRM gene is one such epigenetically silenced gene in Rhabdoid tumors. This gene codes for an ATPase catalytic subunit that shifts histones and opens the ...

Journal: :Journal of the National Cancer Institute 2000
J Savla T T Chen N R Schneider C F Timmons O Delattre G E Tomlinson

Rhabdoid tumor of the kidney is a rare and aggressive childhood cancer (1). Although the infant kidney is the most common site of rhabdoid tumors, these tumors occasionally occur at other sites and in older children and adults (2,3). Less than 25% of infants and young children with rhabdoid tumor of the kidney survive (4,5). Rhabdoid tumor is defined histologically by large cells, which may res...

Journal: :Practica Oto-Rhino-Laryngologica 1991

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