ArticleCase reports in medicine2012
Ewing sarcoma/primitive neuroectodermal tumor of the kidney: two unusual presentations of a rare tumor.
Article in Case reports in medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Anesthesia and perioperative management for giant adrenal Ewing's sarcoma with inferior vena cava and right atrium tumor thrombus: A case report.World journal of clinical cases · 2022Article
- Ureteral Ewing's sarcoma in an elderly woman: A case report.World journal of clinical cases · 2019Article
- Primary Ewing sarcoma of the kidney: a case report and treatment review.CEN case reports · 2017Article
- Renal Primitive Neuroectodermal Tumour: Case Report of a Rare Entity.Journal of clinical and diagnostic research : JCDR · 2017Article
- PNET of the Abdominal Wall: A Rare Presentation.Journal of clinical and diagnostic research : JCDR · 2015Article
- Peripheral primitive neuroectodermal tumor of the kidney presenting with pulmonary tumor embolism: A case report.World journal of radiology · 2014Article
- Renal primitive neuroectodermal tumour: Case series and brief review.Canadian Urological Association journal = Journal de l'Association des urologues du Canada · 2014Article
- Primary Ewing sarcoma of the kidney: a symptomatic presentation and review of the literature.Therapeutic advances in urology · 2013Article
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Authors and funding
2 authors.
Funding
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Abstract
Only few cases of primary renal Ewing's sarcoma have been reported in the literature to date. We present here two cases of renal ES/PNET with an uncanny presentation. The first case was discovered after the patient presented clinically with irradiating flank pain, mimicking the pain related with kidney stones. The second case had clinical presentation of pulmonary thromboembolism after the patient was involved in an automobilist accident. The tumors were mainly composed of small blue cells which by immunohistochemical were positive for neural markers, and FISH revealed the translocation 22q12 for the EWSR1 gene. The diagnosis of renal primitive neuroectodermal tumor/EWING tumor is very rare and usually involves several different diagnostic techniques. The differential diagnosis is usually broad with frequent overlapping features between the entities. The cases presented in this paper illustrated the difficulties with which routine anatomical pathologist is faced when dealing with rare renal poorly differentiated neoplasm in adults.
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