Pleomorphic Rhabdomyosarcoma

2020 ◽  
pp. 663-664
Author(s):  
Simone Mocellin
2021 ◽  
Vol 77 (18) ◽  
pp. 2605
Author(s):  
Clint Jones ◽  
Patrick McGrade ◽  
Priscilla Powell ◽  
Gibbs Wilson ◽  
Margaret Happel

2004 ◽  
Vol 36 (4) ◽  
pp. 577-578 ◽  
Author(s):  
A. Demir ◽  
F.F. �nol ◽  
L. T�rkeri

2017 ◽  
Author(s):  
John Groundland ◽  
Sara Shaw ◽  
R L Randall

Rhabdomyosarcoma (RMS) is a group of soft tissue sarcomas that share a common feature of primitive skeletal muscle differentiation. Three main subtypes have been characterized: embryonal, alveolar, and pleomorphic. Presentation and prognosis of RMS are highly variable, depending on anatomic location, subtype, and risk stratification. Currently, treatment centers on systemic control with cytotoxic chemotherapy and local control with surgery and/or therapeutic radiation. This review contains 3 figures, 10 tables and 50 references  Key words: alveolar rhabdomyosarcoma, embryonal rhabdomyosarcoma, pediatric soft tissue sarcoma, pleomorphic rhabdomyosarcoma, rhabdomyosarcona, t(2;13), t(1;13)


2014 ◽  
Vol 2014 (jan30 1) ◽  
pp. bcr2013203257-bcr2013203257 ◽  
Author(s):  
F. Caporlingua ◽  
G. Lapadula ◽  
M. Antonelli ◽  
P. Missori

2010 ◽  
Vol 222 (2) ◽  
pp. 129-137 ◽  
Author(s):  
Brendan Doyle ◽  
Jennifer P Morton ◽  
David W Delaney ◽  
Rachel A Ridgway ◽  
Julie A Wilkins ◽  
...  

2021 ◽  
pp. 38-40
Author(s):  
S. Kanimozhi ◽  
P. Pooja sri ◽  
P. Karthika ◽  
M. Sathish Kumar ◽  
A. Mathan Mohan

Rhabdomyosarcoma (RMS) is a rare, aggressive, malignant mesenchymal tumor of skeletal muscle cells. The pleomorphic histological variant of RMS occurs in adults beyond 45years of age and represents the most aggressive subtype with an incidence of approximately 0.44/100,000. The diagnosis of RMS is difcult with the 5year overall survival rate less than 50%. It presents varied clinical and biological behavior and requires individualized management. The common region of metastasis includes lymph nodes, lungs and bone marrow. Here we report a case of pleomorphic rhabdomyosarcoma in 58year old female. The patient reported with a swelling in the neck region and had a history of surgical treatment for ovarian tumor. Histopathology ndings revealed metastatic undifferentiated carcinoma. The case was positive for immunohistochemistry markers and their ndings are diagnosed as pleomorphic rhabdomyosarcoma. This is a rare case of RMS which had metastasized to head and neck and this article emphasizes the importance of IHC in accurate and clear diagnosis of RMS.


2015 ◽  
Vol 88 (3) ◽  
pp. E208-E209 ◽  
Author(s):  
Jonathan Kam ◽  
Yuigi Yuminaga ◽  
Fiona Maclean ◽  
Mark Louie-Johnsun

2010 ◽  
Vol 29 (2) ◽  
pp. 122-134 ◽  
Author(s):  
Oluwole Fadare ◽  
Amanda Bonvicino ◽  
Maritza Martel ◽  
Idris L. Renshaw ◽  
Masoud Azodi ◽  
...  

2004 ◽  
Vol 130 (2-3) ◽  
pp. 195-198 ◽  
Author(s):  
T.S. Zabka ◽  
E.L. Buckles ◽  
F.M.D. Gulland ◽  
M. Haulena ◽  
D.K. Naydan ◽  
...  

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