A RARE CASE OF EXTRASKELETAL EWING SARCOMA TUMOR DEVELOPING IN AN UNCOMMON LOCATION—FLOOR OF THE MOUTH

2021 ◽  
Vol 132 (1) ◽  
pp. e22-e23
Author(s):  
J Patel ◽  
F Cristina ◽  
M Amandeep ◽  
K Anand
2015 ◽  
Vol 9 (9-10) ◽  
pp. 648 ◽  
Author(s):  
Jong Wook Kim ◽  
Ji Yun Chae ◽  
Cheol Yong Yoon ◽  
Mi Mi Oh ◽  
Hong Seok Park ◽  
...  

We recently encountered an extremely rare case of spontaneous perirenal hemorrhage in a 34-year-old man. He initially had undergone radical nephrectomy owing to suspicion of renal cell carcinoma. The final diagnosis was extraskeletal Ewing sarcoma.


Author(s):  
Shahryar Bashiri ◽  
Hossein Heidar ◽  
Milad Parvin

Extraskeletal Ewing sarcoma (EES) is an uncommon tumor with low prevalence in the head and neck region. Herein, we report a 13-year-old boy with EES in the temporal region, which was managed by surgery and chemotherapy. The histological characteristics and the clinical manifestations of the lesion and our surgical approach will be discussed as well.


2016 ◽  
Vol 40 (5) ◽  
pp. 843-845 ◽  
Author(s):  
Aaron W.P. Maxwell ◽  
Stephanie Wood ◽  
Damian E. Dupuy

2018 ◽  
Vol 23 (2) ◽  
pp. 430-432
Author(s):  
Khodamorad Jamshidi ◽  
Alireza Mirzaei ◽  
Abolfazl Bagherifard ◽  
Mehrdad Bahrabadi

2003 ◽  
Vol 48 (1) ◽  
pp. 85 ◽  
Author(s):  
Kijun Kim ◽  
Hyun Seouk Jung ◽  
Jae Hee Lee ◽  
Kyung Myung Sohn ◽  
Sung Yong Lee

2017 ◽  
Author(s):  
Vassilios Papadakis ◽  
Elpis Vlachopapadopoulou ◽  
Kondylia Antoniadi ◽  
Vassiliki Tzotzola ◽  
John Nikas ◽  
...  
Keyword(s):  

2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Hyma Polimera ◽  
Prashanth Moku ◽  
Shady Piedra Abusharar ◽  
Monali Vasekar ◽  
Jayakrishna Chintanaboina

Ewing sarcoma (ES) is a highly aggressive malignant bone cancer. ES is part of the Ewing sarcoma family of tumors (ESFT), which express characteristic t(11;22) translocation as well as higher levels of CD99. Given that metastasis and tumor burden are significant prognostic factors in patient’s response to treatment, prompt diagnosis is needed to effectively treat ESFT patients. However, the challenges in classifying and characterizing ESFT complicate effective management and treatment of ES. In this report, we present a rare case of ES metastasis to the pancreas. Upon review of the literature, we found 39 cases of ESFT involving the pancreas, but only 3 were metastatic to the pancreas while the remaining cases of ESFT primarily originated from the pancreas. Given the rarity of such metastasis, the positive outcome in our patient’s case may explain the importance of prompt diagnosis in order to initiate appropriate treatment.


2011 ◽  
Vol 285 (3) ◽  
pp. 785-789 ◽  
Author(s):  
Katharina Kelling ◽  
Frank Noack ◽  
Christopher Altgassen ◽  
Peter Kujath ◽  
Michael K. Bohlmann ◽  
...  

2021 ◽  
Vol 80 ◽  
pp. 105676
Author(s):  
Tomohiko Sakuda ◽  
Taisuke Furuta ◽  
Muhammad Phetrus Johan ◽  
Koji Arihiro ◽  
Nobuo Adachi

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