Ewing’s sarcoma/primitive neuroectodermal tumor of the prostate a case report and literature review

2013 ◽  
Vol 7 (5-6) ◽  
Author(s):  
Tao Wu ◽  
Tao Jin ◽  
Deyi Luo ◽  
Lin Chen ◽  
Xiang Li
Keyword(s):  
Primitive Neuroectodermal Tumor ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Transrectal Ultrasound ◽  
Neuroectodermal Tumor ◽  
Resonance Imaging ◽  
Mri Scan ◽  
Difficult Defecation ◽  
Magnetic Resonance Imaging Mri ◽  
Multiagent Chemotherapy

We present a case of Ewing’s sarcoma (ES) and primitive neuroectodermal tumor (PNET) of prostate. A 29-year-old male presented with difficult defecation and anus distention and was found on magnetic resonance imaging (MRI) scan of the pelvis to have a prostate tumor. A transrectal ultrasound guided needle biopsy confirmed the diagnosis. The patient underwent cystoprostatectomy and replacement ileocystoplasty and was followed by multiagent chemotherapy. PNET/EWS of the prostate is an extremely rare neoplasm. And the prognosis is very poor, so we should pay enough attention to the differential diagnosis and treatment.

scholarly journals Ewing’s sarcoma/primitive neuroectodermal tumour of the prostate a case report and literature review

2013 ◽  
Vol 7 (5-6) ◽  
pp. 458 ◽  
Author(s):  
Tao Wu ◽  
Tao Jin ◽  
Deyi Luo ◽  
Lin Chen ◽  
Xiang Li
Keyword(s):  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Transrectal Ultrasound ◽  
Magnetic Resonance Imaging Scan ◽  
Resonance Imaging ◽  
Ultrasound Guided ◽  
Primitive Neuroectodermal Tumour ◽  
Neuroectodermal Tumour ◽  
Multi Agent ◽  
Difficult Defecation

We present a case of Ewing’s sarcoma and primitive neuroectodermal tumour (PNET) of the prostate. A 29-year-old male presented with difficult defecation and anus distention; on magnetic resonance imaging scan of the pelvis, we found a prostate tumour. A transrectal ultrasound-guided needle biopsy confirmed the diagnosis. The patient underwent cystoprostatectomy and replacement ileocystoplasty and was followed by multi-agent chemotherapy. PNET/ Ewing’s sarcoma of the prostate is extremely rare. The prognosis is very poor, so we should pay enough attention to the differential diagnosis and treatment.

scholarly journals Unusual Presentation of Peripheral Primitive Neuroectodermal Tumor: A Rare Case Report

2021 ◽  
Vol 5 (3) ◽  
pp. 358
Author(s):  
Kanika Singh ◽  
Sujata Raychaudhuri ◽  
Varsha Chauhan ◽  
Akanksha Bajaj ◽  
Reetika Menia
Keyword(s):  
Soft Tissue ◽  
Primitive Neuroectodermal Tumor ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Final Diagnosis ◽  
Neuroectodermal Tumor ◽  
Elderly Male ◽  
Tissue Mass ◽  
Rare Case Report ◽  
Multiagent Chemotherapy

A primitive neuroectodermal tumor (PNET) is a rare entity occurring most commonly in the 2nd and 3rd decade and is very rare in patients over 40 years of age. PNET is a round cell malignancy of presumably primitive neuroectodermal tissue or migratory neural crest cells arising from soft tissue or bone. PNET occurring outside the central nervous system is called peripheral PNET (p PNET) and most commonly involves the trunk and extremities Here we present a case of PNET diagnosed in an elderly male who presented with a soft tissue mass in the gluteal region. The histopathology with ancillary techniques including immunohistochemistry and molecular studies helped in establishing the diagnosis of PNET. They are characterized by translocation leading to the fusion of Ewing’s Sarcoma (EWS) gene on 22q12 with any of the member of the ETS (E 26 transformation specific or E -twenty – six) family of transcription factors with the most frequent being t (11;22) (q24;12). Intensive multiagent chemotherapy is the mainstay of treatment as it has great potential for metastatic spread. The prognosis of adults with Ewing’s sarcoma (ES)/PNET is not well known, however, some reports suggested that adults with ES/PNET have a poorer prognosis than children. Cytology is the first line of diagnosis for RCT. However, the type-specific diagnosis or final diagnosis of p PNET is based on histopathology aided with IHC and other ancillary techniques.International Journal of Human and Health Sciences Vol. 05 No. 03 July’21 Page: 358-361

Primary Ewing's Sarcoma/Primitive Neuroectodermal Tumor of Kidney with Caval Involvement in a Pregnant Woman

2016 ◽  
Vol 97 (3) ◽  
pp. 365-368 ◽  
Author(s):  
Yinghui Ding ◽  
Zhenlin Huang ◽  
Yafei Ding ◽  
Zhankui Jia ◽  
Chaohui Gu ◽  
...  
Keyword(s):  
Pregnant Woman ◽  
Primitive Neuroectodermal Tumor ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Neuroectodermal Tumor

Primitive neuroectodermal tumor/Ewing's sarcoma: a case report and literature review

2017 ◽  
Vol 176 (10) ◽  
Author(s):  
Izabela S. Alves ◽  
Luiz G. Berriel ◽  
Rafael T. Alves ◽  
Mateus O. Potratz ◽  
Marcele B. Pinto ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Primitive Neuroectodermal Tumor ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Neuroectodermal Tumor

scholarly journals Primary Pulmonary Ewing's Sarcoma/Primitive Neuroectodermal Tumor in a 67-year-old Man

2007 ◽  
Vol 22 (Suppl) ◽  
pp. S159 ◽  
Author(s):  
Yoon Young Lee ◽  
Do Hoon Kim ◽  
Ji Hye Lee ◽  
Jong Sang Choi ◽  
Kwang Ho In ◽  
...  
Keyword(s):  
Primitive Neuroectodermal Tumor ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Neuroectodermal Tumor

A rare case of Ewing's sarcoma/primitive neuroectodermal tumor metastasizing to left atrium through left inferior pulmonary vein

2018 ◽  
Vol 35 (6) ◽  
pp. 885-888 ◽  
Author(s):  
Suraj K. Kulkarni ◽  
Nagaraj Moorthy ◽  
Shankar Somanna ◽  
Manjunath Cholenahally Nanjappa
Keyword(s):  
Left Atrium ◽  
Pulmonary Vein ◽  
Rare Case ◽  
Primitive Neuroectodermal Tumor ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Neuroectodermal Tumor ◽  
Inferior Pulmonary Vein
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