Primary metastasized extraskeletal Ewing sarcoma of the vulva: report of a case and review of the literature

2011 ◽  
Vol 285 (3) ◽  
pp. 785-789 ◽  
Author(s):  
Katharina Kelling ◽  
Frank Noack ◽  
Christopher Altgassen ◽  
Peter Kujath ◽  
Michael K. Bohlmann ◽  
...  
Keyword(s):  
Ewing Sarcoma ◽  
Review Of The Literature ◽  
Extraskeletal Ewing Sarcoma

Extraskeletal Ewing Sarcoma of Cervical Epidural Region: Cases Report

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

scholarly journals Metastasis of Ewing Sarcoma to the Pancreas: Case Report and Literature Review

2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Hyma Polimera ◽  
Prashanth Moku ◽  
Shady Piedra Abusharar ◽  
Monali Vasekar ◽  
Jayakrishna Chintanaboina
Keyword(s):  
Ewing Sarcoma ◽  
Rare Case ◽  
Bone Cancer ◽  
Positive Outcome ◽  
Tumor Burden ◽  
Response To Treatment ◽  
Effective Management ◽  
Review Of The Literature ◽  
Appropriate Treatment ◽  
Prompt Diagnosis

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.

scholarly journals Extraskeletal Ewing sarcoma attached to the ulnar nerve: A case report

2021 ◽  
Vol 80 ◽  
pp. 105676
Author(s):  
Tomohiko Sakuda ◽  
Taisuke Furuta ◽  
Muhammad Phetrus Johan ◽  
Koji Arihiro ◽  
Nobuo Adachi
Keyword(s):  
Case Report ◽  
Ulnar Nerve ◽  
Ewing Sarcoma ◽  
Extraskeletal Ewing Sarcoma

Extraskeletal Ewing Sarcoma

2020 ◽  
pp. 311-316
Author(s):  
Simone Mocellin
Keyword(s):  
Ewing Sarcoma ◽  
Extraskeletal Ewing Sarcoma

scholarly journals Large extraskeletal ewing sarcoma of the hand: A rare entity

2019 ◽  
Vol 18 (3) ◽  
pp. 177 ◽  
Author(s):  
Sonal Saran ◽  
Annu Kharbanda ◽  
Sunil Malik
Keyword(s):  
Ewing Sarcoma ◽  
Rare Entity ◽  
Extraskeletal Ewing Sarcoma

A CASE REPORT OF A YOUNG MAN WITH ABDOMINAL MASS: HUNT FOR DIAGNOSIS

2021 ◽  
pp. 55-56
Author(s):  
K Pratyusha ◽  
Satish Arakeri ◽  
Surekha Arakeri
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Liver Abscess ◽  
Ewing Sarcoma ◽  
Abdominal Mass ◽  
Histopathological Study ◽  
Round Cell ◽  
Small Round Cell ◽  
Malignant Soft Tissue Tumor ◽  
Extraskeletal Ewing Sarcoma

Introduction: Extraskeletal Ewing sarcoma/PNET is a small round cell sarcoma showing gene fusions of EWSR1-FLI1. A 28-year-old male patient presented with right ank pain and low gr Case Report: ade fever since 15 days. On examination: a mass was palpable in the right hypochondrium. Provisional diagnosis of Liver abscess has been made. USG abdomen shows features cystic lesion in the liver with internal septation ?Liver abscess /Hydatid cyst. Intraoperatively, tumor was seen attached to upper pole of kidney. Since tumor was large, it was ruptured intraoperatively and debulking surgery has been done. Under microscopy, tumor was arranged in sheets with intervening stroma showing desmoplastic reaction. Perivascular pseudorosettes are seen. The diagnosis of malignant small round cell tumor has been given. On immunohistochemistry, tumor cells are positive for Vimentin, CD99, NKX2.2 , FLI1, Neurolaments, Synaptophysin with focal immunoreactivity for EMA, Pancytokeratin. Final diagnosis was EXTRASKELETAL EWING SARCOMA/PNET. Discussion: Extra-skeletal Ewing sarcoma/PNET is malignant soft tissue tumor seen in chest wall, thigh, paravertebal region etc. Retroperitoneum is a least common site. Most common presentation is swelling in the soft tissue with compressive symptoms. Histologically, it is composed of undifferentiated small round cells. Conclusion: Clinical examination and radiological ndings leads to ambiguous diagnosis in Ewing sarcoma/PNET. Hence proper histopathological study is essential for nal diagnosis.

scholarly journals Primary Ewing sarcoma of the kidney: a symptomatic presentation and review of the literature

2012 ◽  
Vol 5 (3) ◽  
pp. 153-159 ◽  
Author(s):  
Tariq S. Hakky ◽  
Americo A. Gonzalvo ◽  
Jorge L. Lockhart ◽  
Alejandro R. Rodriguez
Keyword(s):  
Ewing Sarcoma ◽  
Review Of The Literature

Extraskeletal Ewing sarcoma of the diaphragm presenting with hemothorax

2004 ◽  
Vol 78 (2) ◽  
pp. 715-717 ◽  
Author(s):  
Atilla Eroğlu ◽  
İbrahim Can Kürkçüoğlu ◽  
Nurettin Karaoğlanoğlu ◽  
Fatih Alper ◽  
Cemal Gündoğdu
Keyword(s):  
Ewing Sarcoma ◽  
Extraskeletal Ewing Sarcoma
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