Bilateral Adrenal PNET: A Rare Presentation

Primitive neuroectodermal tumours or PNET's are rare, malignant tumours with aggressive course and extremely poor prognosis. They have no sex preference. They arise mostly in the second decade of life. They are believed to be of neural crest origin and carry the name primitive because majorit...

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Main Authors: Santosh Kumar, Vijayant Govinda, Shravan Kumar Singh, Jyotsana Singh
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2016-09-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/8397/9260_CE(Ra1)_F(GH)_PF1(VIAK)_PFA(NC_AK)_PF2(PAG).pdf
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spelling doaj-37b9566ceff9435a9afc25dc434a04c52020-11-25T03:44:08ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2016-09-01109XD01XD0210.7860/JCDR/2016/9260.8397Bilateral Adrenal PNET: A Rare PresentationSantosh Kumar0Vijayant Govinda1Shravan Kumar Singh2Jyotsana Singh3Assistant Professor, Department of Urology, PGIMER, Chandigarh, India.Senior Resident, Department of Urology, PGIMER, Chandigarh, India.Professor, Department of Urology, PGIMER, Chandigarh, India.Clinical Attaché, Department of Urology, PGIMER, Chandigarh, India.Primitive neuroectodermal tumours or PNET's are rare, malignant tumours with aggressive course and extremely poor prognosis. They have no sex preference. They arise mostly in the second decade of life. They are believed to be of neural crest origin and carry the name primitive because majority of the neuronal cells in these tumours appear undifferentiated. Solid organ origin is very rare and tumours arising from the adrenals are very infrequent. We report a case of metastatic bilateral adrenal PNET in a 45-year-old man. We believe this to be the first such case reported in the urological literature. https://jcdr.net/articles/PDF/8397/9260_CE(Ra1)_F(GH)_PF1(VIAK)_PFA(NC_AK)_PF2(PAG).pdfadrenal tumourneural crest originprimitive neuroectodermal tumour
collection DOAJ
language English
format Article
sources DOAJ
author Santosh Kumar
Vijayant Govinda
Shravan Kumar Singh
Jyotsana Singh
spellingShingle Santosh Kumar
Vijayant Govinda
Shravan Kumar Singh
Jyotsana Singh
Bilateral Adrenal PNET: A Rare Presentation
Journal of Clinical and Diagnostic Research
adrenal tumour
neural crest origin
primitive neuroectodermal tumour
author_facet Santosh Kumar
Vijayant Govinda
Shravan Kumar Singh
Jyotsana Singh
author_sort Santosh Kumar
title Bilateral Adrenal PNET: A Rare Presentation
title_short Bilateral Adrenal PNET: A Rare Presentation
title_full Bilateral Adrenal PNET: A Rare Presentation
title_fullStr Bilateral Adrenal PNET: A Rare Presentation
title_full_unstemmed Bilateral Adrenal PNET: A Rare Presentation
title_sort bilateral adrenal pnet: a rare presentation
publisher JCDR Research and Publications Private Limited
series Journal of Clinical and Diagnostic Research
issn 2249-782X
0973-709X
publishDate 2016-09-01
description Primitive neuroectodermal tumours or PNET's are rare, malignant tumours with aggressive course and extremely poor prognosis. They have no sex preference. They arise mostly in the second decade of life. They are believed to be of neural crest origin and carry the name primitive because majority of the neuronal cells in these tumours appear undifferentiated. Solid organ origin is very rare and tumours arising from the adrenals are very infrequent. We report a case of metastatic bilateral adrenal PNET in a 45-year-old man. We believe this to be the first such case reported in the urological literature.
topic adrenal tumour
neural crest origin
primitive neuroectodermal tumour
url https://jcdr.net/articles/PDF/8397/9260_CE(Ra1)_F(GH)_PF1(VIAK)_PFA(NC_AK)_PF2(PAG).pdf
work_keys_str_mv AT santoshkumar bilateraladrenalpnetararepresentation
AT vijayantgovinda bilateraladrenalpnetararepresentation
AT shravankumarsingh bilateraladrenalpnetararepresentation
AT jyotsanasingh bilateraladrenalpnetararepresentation
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