scholarly journals Rare spindle cell hemangioma of bone: Case report and literature review

2022 ◽  
Vol 17 (3) ◽  
pp. 886-890
Author(s):  
Cong Huang ◽  
Hengsheng Zhang ◽  
Li Guan ◽  
Junde Luo
2010 ◽  
Vol 163 (3) ◽  
pp. 638-640 ◽  
Author(s):  
T. Agostini ◽  
C. Catelani ◽  
A. Acocella ◽  
A. Franchi ◽  
R. Bertolai ◽  
...  

Andrologia ◽  
2022 ◽  
Author(s):  
Yufeng Song ◽  
Hao Ning ◽  
Zhigang Yao ◽  
Haihu Wu ◽  
Jinglong Shao ◽  
...  

2019 ◽  
Vol 2 (1) ◽  
pp. 1-3
Author(s):  
Alexis Eduardo Higareda Basilio ◽  
Cecilio Omar Ceballos Zuñiga ◽  
Federico Isaac Hernandez Rocha ◽  
Sara Sofía Yaurima Ham

Author(s):  
Ursula M. Jariod–Ferrer ◽  
Miguel Angel Trigo-Cebrian ◽  
Bianca Pantilie ◽  
María V. Simon Sanz ◽  
Leire Esparza Lasaga ◽  
...  

2012 ◽  
Vol 12 (2) ◽  
pp. 147-150 ◽  
Author(s):  
Rita Nonnis ◽  
Panagiotis Paliogiannis ◽  
Daiana Giangrande ◽  
Vincenzo Marras ◽  
Mario Trignano

2014 ◽  
Vol 30 (5) ◽  
pp. 291-293
Author(s):  
Sarah H. Kim ◽  
Nigel Pereira ◽  
Jennifer Hawkins ◽  
Beth C. Mapow ◽  
Scott D. Richard

2003 ◽  
Vol 10 (7) ◽  
pp. 393-395 ◽  
Author(s):  
Linda SL Cheng ◽  
Gary MK Tse ◽  
Wilson WL Li ◽  
TW Lee ◽  
Anthony PC Yim

Synovial sarcomas are uncommon soft tissue tumours. Immunohistochemistry and cytogenetic techniques are essential for proper diagnosis and differentiation from other spindle cell neoplasms. A case of mediastinal synovial sarcoma is described, of which the unusual location, diagnosis and treatment form the basis of this report.


2013 ◽  
Vol 40 (7) ◽  
pp. 661-666 ◽  
Author(s):  
Yu Cai ◽  
Rong Wang ◽  
Xin-Ming Chen ◽  
Yi-Fang Zhao ◽  
Zhi-Jun Sun ◽  
...  

2016 ◽  
Vol 121 (3) ◽  
pp. e54-e61 ◽  
Author(s):  
Yuki Matsushita ◽  
Shuichi Fujita ◽  
Souichi Yanamoto ◽  
Shin-ichi Yamada ◽  
Satoshi Rokutanda ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Mario Metry ◽  
Mohamad Shaaban ◽  
Magdi Youssef ◽  
Michael Carr

Myofibroblastoma of the breast is a rare benign spindle cell tumor. The main aim of this study is to review the literature of this rare tumor. We present a case of a mammary myofibroblastoma occurring in an 82-year-old man, emphasizing the clinical, radiological, and pathological features. The tumor was successfully identified and managed in our hospital. We would like to draw the attention of clinicians to myofibroblastoma as a rare possibility in the differential diagnosis of a breast mass.


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