Literature DB >> 14647620

[Primitive neuroectodermal tumor of the kidney in children]

A P Kuczynski1, E S Gugelmin, R A Netto.   

Abstract

OBJECTIVES: To characterize primitive neuroectodermal tumor of the kidney as a differential diagnosis for Wilms tumor, and to emphasize the severity of the disease.
METHODS: We report the case of a patient with a diagnosis of primitive neuroectodermal tumor of the kidney who underwent nephrectomy and complete tumor resection combined with chemotherapy.
RESULTS: Initially, the response of the patient to treatment was favorable, with a few events associated with agranulocytosis resulting from the chemotherapy. Ten months after of the end of treatment, the tumor recurred in the paraspinal cervical region.
CONCLUSIONS: Primitive neuroectodermal tumors involving the kidney are very rare and extremely aggressive. In such cases, the pathologist has a major role in establishing a final diagnosis through histological and immunohistochemical methods.

Entities:  

Year:  2001        PMID: 14647620     DOI: 10.2223/jped.111

Source DB:  PubMed          Journal:  J Pediatr (Rio J)        ISSN: 0021-7557            Impact factor:   2.197


  3 in total

1.  Primary Ewing sarcoma of the kidney: a case report and treatment review.

Authors:  Muhammad Sadiq; Iftikhar Ahmad; Jamila Shuja; Khushnaseeb Ahmad
Journal:  CEN Case Rep       Date:  2017-04-21

Review 2.  Primitive neuroectodermal tumor of the kidney: case report and review of literature.

Authors:  Chuanyu Sun; Zunguo Du; Shijun Tong; Ke Xu; Weihong Ding; Jianliang Sun; Qiang Ding
Journal:  World J Surg Oncol       Date:  2012-12-27       Impact factor: 2.754

3.  Primary Renal Primitive Neuroectodermal Tumor/Ewing's Sarcoma Imaging and Pathologic Findings of a Patient with a Nine Year, Eight Month Disease Free Period: Case Report and Review of Literature.

Authors:  Ivan Zokalj; Jasminka Igrec; Antonio Plesnar
Journal:  Nephrourol Mon       Date:  2016-07-18
  3 in total

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