Literature DB >> 22430589

PNET spine: morbid and mortal, but ignored till late.

Ram Prabu1, Sanjay Thulkar, Mehar Chand Sharma, Bidhu K Mohanti, Deepa Dhawan, Sameer Bakhshi.   

Abstract

Spinal primitive neuroectodermal tumor (PNET) is rare. We present clinical, radiologic profile and treatment outcome of 15 spinal PNET patients from June 2003 to March 2010 treated with chemoradiotherapy. Median duration of backache was 6.5 months; all had features of myelopathy and/or radiculopathy; 5/15 (33.3%) patients were diagnosed initially as spinal tuberculosis. The event-free survival (EFS) was 24.73% at a median follow-up of 22 months. Complete functional recovery to treatment significantly predicted better EFS; 4 patients discontinued treatment because of poor functional recovery. It is important to recognize spinal PNET early to prevent permanent neurological damage, which in turn would improve compliance, quality of life, and perhaps EFS.

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Year:  2012        PMID: 22430589     DOI: 10.1097/MPH.0b013e31824414b2

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  2 in total

1.  Clinical, pathological, and imaging characteristics of primitive neuroectodermal tumors of the spine.

Authors:  Hong Guobin; Gu Lingjing; Ding Xianglian; Song Liqing; Peng Hong; Xu Qilan
Journal:  Diagn Interv Radiol       Date:  2014 Mar-Apr       Impact factor: 2.630

Review 2.  Indian data on bone and soft tissue sarcomas: A summary of published study results.

Authors:  Anant Ramaswamy; Bharat Rekhi; Sameer Bakhshi; Sachin Hingmire; Manish Agarwal
Journal:  South Asian J Cancer       Date:  2016 Jul-Sep
  2 in total

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