Intraneural synovial sarcoma of median nerve

Synovial sarcomas are highly aggressive soft tissue tumour with a poor and dismal prognosis. These tumours have a high propensity for distant metastasis and local recurrence.  Although originally believed to arise from synovium, these tumours have been found to occur anywhere in body1,2. We report h...

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Main Authors: Sandeep Bhardwaj, Anil Kansal, Rohit Bansal, Rakesh Sharma, Akangsha Sharma
Format: Article
Language:English
Published: London Academic Publishing 2020-03-01
Series:Romanian Neurosurgery
Subjects:
Online Access:https://www.journals.lapub.co.uk/index.php/roneurosurgery/article/view/1349
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author Sandeep Bhardwaj
Anil Kansal
Rohit Bansal
Rakesh Sharma
Akangsha Sharma
author_facet Sandeep Bhardwaj
Anil Kansal
Rohit Bansal
Rakesh Sharma
Akangsha Sharma
author_sort Sandeep Bhardwaj
collection DOAJ
description Synovial sarcomas are highly aggressive soft tissue tumour with a poor and dismal prognosis. These tumours have a high propensity for distant metastasis and local recurrence.  Although originally believed to arise from synovium, these tumours have been found to occur anywhere in body1,2. We report here, a case of median nerve sarcoma in a 15-year female. This is a rare tumour, which is diagnosed only after histopathological examination with only a few cases reported in the literature (Table 1). Although preoperatively tumour was thought to be a nerve sheath tumour, on histopathology analysis was found to be synovial sarcoma. Despite aggressive behaviour, wide local excision is recommended even in smaller lesions. So, the diagnosis should always be kept in differentials of nerve sheath tumour, as what may be a synovial sarcoma.
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spelling doaj.art-ee6c050ee3974b9a8f0d611e61de56ce2022-12-21T21:56:17ZengLondon Academic PublishingRomanian Neurosurgery1220-88412344-49592020-03-01341Intraneural synovial sarcoma of median nerveSandeep BhardwajAnil KansalRohit BansalRakesh SharmaAkangsha SharmaSynovial sarcomas are highly aggressive soft tissue tumour with a poor and dismal prognosis. These tumours have a high propensity for distant metastasis and local recurrence.  Although originally believed to arise from synovium, these tumours have been found to occur anywhere in body1,2. We report here, a case of median nerve sarcoma in a 15-year female. This is a rare tumour, which is diagnosed only after histopathological examination with only a few cases reported in the literature (Table 1). Although preoperatively tumour was thought to be a nerve sheath tumour, on histopathology analysis was found to be synovial sarcoma. Despite aggressive behaviour, wide local excision is recommended even in smaller lesions. So, the diagnosis should always be kept in differentials of nerve sheath tumour, as what may be a synovial sarcoma.https://www.journals.lapub.co.uk/index.php/roneurosurgery/article/view/1349intraneural synovial sarcomamedian nervearmsoft tissue tumour
spellingShingle Sandeep Bhardwaj
Anil Kansal
Rohit Bansal
Rakesh Sharma
Akangsha Sharma
Intraneural synovial sarcoma of median nerve
Romanian Neurosurgery
intraneural synovial sarcoma
median nerve
arm
soft tissue tumour
title Intraneural synovial sarcoma of median nerve
title_full Intraneural synovial sarcoma of median nerve
title_fullStr Intraneural synovial sarcoma of median nerve
title_full_unstemmed Intraneural synovial sarcoma of median nerve
title_short Intraneural synovial sarcoma of median nerve
title_sort intraneural synovial sarcoma of median nerve
topic intraneural synovial sarcoma
median nerve
arm
soft tissue tumour
url https://www.journals.lapub.co.uk/index.php/roneurosurgery/article/view/1349
work_keys_str_mv AT sandeepbhardwaj intraneuralsynovialsarcomaofmediannerve
AT anilkansal intraneuralsynovialsarcomaofmediannerve
AT rohitbansal intraneuralsynovialsarcomaofmediannerve
AT rakeshsharma intraneuralsynovialsarcomaofmediannerve
AT akangshasharma intraneuralsynovialsarcomaofmediannerve