Noninvasive Ewing's Sarcoma of the Penis: A Rare Entity

Urology ◽  
2020 ◽  
Vol 144 ◽  
pp. e15-e18
Author(s):  
Gabrielle R. Yankelevich ◽  
Javier Piraino ◽  
Daniel Edwards ◽  
Jeremy Molligan ◽  
Guy T. Bernstein
Keyword(s):  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Rare Entity

scholarly journals Ewing’s sarcoma of sinonasal tract: a rare case

2020 ◽  
Vol 6 (3) ◽  
pp. 565
Author(s):  
Ankur Gupta ◽  
Ancy S. Sofia ◽  
Kanwar Sen
Keyword(s):  
Multidisciplinary Approach ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Histopathological Examination ◽  
Malignant Tumour ◽  
Rare Entity ◽  
Round Cell ◽  
First Line ◽  
Cytogenetic Studies ◽  
Immunohistochemical Studies

<p class="abstract">Extra skeletal Ewing’s sarcoma (EES) is a rare, rapidly growing, round cell malignant tumour that can develop in the soft tissue at any location. Involvement of the paranasal sinus is a very rare entity. Nearly 80% of patients are younger than 20 years. Diagnosis is made after histopathological examination, immunohistochemical studies and cytogenetic studies. Treatment includes a multidisciplinary approach with surgery as the first line followed by chemotherapy and radiotherapy.</p><p class="abstract"> </p>

scholarly journals Extraosseous Ewing's sarcoma of the maxillary sinus: A very rare entity

2018 ◽  
Vol 39 (3) ◽  
pp. 380 ◽  
Author(s):  
LakshmiKeerthana Killampalli ◽  
ARavi Prakash ◽  
AVikram Simha Reddy ◽  
M Rajinikanth
Keyword(s):  
Maxillary Sinus ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Rare Entity ◽  
Extraosseous Ewing’S Sarcoma

scholarly journals Primary cutaneous extraskeletal Ewing's sarcoma: A case report of an extremely rare entity

2018 ◽  
Vol 22 (1) ◽  
pp. 41
Author(s):  
DianaCosta Santos ◽  
Rui Barbosa ◽  
Rosa Azevedo ◽  
Marco Rebelo ◽  
Carlos Pinho ◽  
...  
Keyword(s):  
Case Report ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Rare Entity ◽  
Extraskeletal Ewing’S Sarcoma

scholarly journals Spinal ewing's Sarcoma presenting as an epidural collection: A rare presentation of a rare entity

2020 ◽  
Vol 15 (2) ◽  
pp. 445
Author(s):  
Sibhi Ganapathy ◽  
Venugopal Subramaniam ◽  
Vidya Baliga
Keyword(s):  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Rare Entity ◽  
Rare Presentation

scholarly journals Primary Ewing’s sarcoma of the temporal bone: a rare entity and review of the literature

2019 ◽  
Vol 12 (10) ◽  
pp. e230768
Author(s):  
Jeewan Ram Vishnoi ◽  
Vijay Kumar ◽  
Kirti Srivastava ◽  
Sanjeev Misra
Keyword(s):  
Temporal Bone ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Bone Tumour ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Radiological Features ◽  
Primary Bone Tumour ◽  
Primary Bone ◽  
Multiagent Chemotherapy

Ewing’s sarcoma (ES) is the second most common malignant primary bone tumour in children and adolescents. It primarily affects the diaphysis of long bones and pelvis. ES arising from temporal bone is extremely rare. To date, 43 such cases have been described in the literature. Clinical and radiological features are non-specific. Diagnosis is based mainly on immunohistochemistry. The present article presents an extremely rare case of ES of the temporal bone in a 20-year young man, and he was successfully treated with multiagent chemotherapy and radiotherapy.

scholarly journals Ewing's sarcoma of scapula: a rare entity

2011 ◽  
Vol 2011 (mar09 1) ◽  
pp. bcr0220113810-bcr0220113810 ◽  
Author(s):  
M. Shahid ◽  
M. Varshney ◽  
V. Maheshwari ◽  
A. Mubeen ◽  
M. A. Siddiqui ◽  
...  
Keyword(s):  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Rare Entity

Dilemma in diagnosis and management of rare primary pleural Ewing’s sarcoma with synchronous limited metastatic disease

2021 ◽  
Vol 14 (6) ◽  
pp. e243495
Author(s):  
Abhijith Bhaskaran ◽  
Pooja Sethi ◽  
Pampa Ch Toi ◽  
Prasanth Penumadu
Keyword(s):  
Metastatic Disease ◽  
Ewing’S Sarcoma ◽  
Treatment Guidelines ◽  
Ewing's Sarcoma ◽  
Rare Entity ◽  
Synchronous Metastases ◽  
Multiagent Chemotherapy ◽  
Metastatic Sites ◽  
Extraosseous Ewing’S Sarcoma ◽  
Limited Metastatic Disease

We present a case of a 34-year-old woman who presented with complaints of fever, cough and dyspnoea of 2 months’ duration. On evaluation, she was diagnosed with a rare entity primary pleural Ewing’s sarcoma with synchronous metastases to mediastinal, supraclavicular nodes and single vertebra. Due to the rarity of this entity and lack of treatment guidelines on extraosseous Ewing’s sarcoma, the patient was managed with a combination of multiagent chemotherapy, surgery and radiotherapy as per standard guidelines for skeletal Ewing’s sarcoma. We present this case to discuss differential diagnoses and management dilemmas encountered on the use of local modalities such as surgery and radiotherapy for control of primary and metastatic sites.

Sign in / Sign up

Export Citation Format

Share Document