Literature DB >> 23120643

Peripheral primitive neuroectodermal tumor of head-neck region: our experience.

Anirban Ghosh1, Somnath Saha, Sudipta Pal, Padmini V Saha, Sarbani Chattopadhyay.   

Abstract

To present four rare cases of peripheral primitive neuroectodermal tumors of different sites of head and neck region. Four cases of different age (range 8-40 years) and sex (three female, one male) with rare primitive neuroectodermal tumor of sinonasal region and neck are presented. Treatment options, biological behavior and prognostic outcome are discussed herewith. Two patients succumbed to the disease within four to six months of treatment; other two patients are still under follow-up depicting the aggressive nature of the tumor. Primitive neuroectodermal tumor belongs to the class of malignant round cell tumor. Immunohistochemistry plays a pivotal role in differentiating this tumor entity. Chemoradiation was tried, but local and systemic spread occurs early and holds poor prognosis. This case series is an attempt to describe the aggressive behavior of this rare tumor with high mortality.

Entities:  

Keywords:  Chemotherapy; Ewing’s sarcoma; Head-neck; Immunostaining; Paranasal sinuses; Primitive neuroectodermal tumor (PNET); Radiation therapy

Year:  2009        PMID: 23120643      PMCID: PMC3449979          DOI: 10.1007/s12070-009-0074-9

Source DB:  PubMed          Journal:  Indian J Otolaryngol Head Neck Surg        ISSN: 2231-3796


  9 in total

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  9 in total
  1 in total

Review 1.  Peripheral primitive neuroectodermal tumors: A retrospective analysis of 89 cases and literature review.

Authors:  Liming Gao; Yingying Zhu; Xiaohua Shi; Zhiqiang Gao; Xingming Chen
Journal:  Oncol Lett       Date:  2019-10-18       Impact factor: 2.967

  1 in total

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