Peripheral Primitive Neuroectodermal Tumour of the Maxilla and Paranasal Sinuses: A Rare Clinical Presentation
Peripheral Primitive Neuroectodermal Tumours (pPNET) are rare aggressive tumours of neural crest cell origin. These tumours are more common in children and young adults. This is a unique report of one such presentation in a 23-year-old lady occurring in the left side posterior maxilla and Paranasa...
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doaj-cfbd5afbdcb64c149e12c465be8f5edd2020-11-25T03:02:21ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2015-05-0195ZD32ZD3410.7860/JCDR/2015/13055.5949Peripheral Primitive Neuroectodermal Tumour of the Maxilla and Paranasal Sinuses: A Rare Clinical PresentationC.L. Krithika0S. Sathasivasubramanian1C. Ponranjini Vedeswari2Senior Lecturer, Department of Oral Medicine & Radiology, SRM Dental College, Bharathi Salai, Ramapuram, Chennai, India.Professor & Head, Department of Oral Medicine & Radiology, Faculty of Dental Sciences, Sri Ramachandra University, Porur, Chennai, India.Assistant Professor, Department of Oral Medicine & Radiology, Thoothukudi Government Medical College, Thoothukudi, India.Peripheral Primitive Neuroectodermal Tumours (pPNET) are rare aggressive tumours of neural crest cell origin. These tumours are more common in children and young adults. This is a unique report of one such presentation in a 23-year-old lady occurring in the left side posterior maxilla and Paranasal sinuses along with imaging characteristics, histopathologic features, immunohistochemical aspects and management. Though these tumours are rare, they should be considered in the differential diagnosis of rapidly growing soft tissue masses in young adults. Precise diagnosis with timely management is necessary for good prognosis. https://jcdr.net/articles/PDF/5949/13055_CE(RA1)_F(T)_PF1(AGAK)_PFA(AK)_PF2(PAG).pdfaggressiveoral cavitysmall round cell tumours |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
C.L. Krithika S. Sathasivasubramanian C. Ponranjini Vedeswari |
spellingShingle |
C.L. Krithika S. Sathasivasubramanian C. Ponranjini Vedeswari Peripheral Primitive Neuroectodermal Tumour of the Maxilla and Paranasal Sinuses: A Rare Clinical Presentation Journal of Clinical and Diagnostic Research aggressive oral cavity small round cell tumours |
author_facet |
C.L. Krithika S. Sathasivasubramanian C. Ponranjini Vedeswari |
author_sort |
C.L. Krithika |
title |
Peripheral Primitive Neuroectodermal Tumour of the Maxilla and Paranasal Sinuses: A Rare Clinical Presentation |
title_short |
Peripheral Primitive Neuroectodermal Tumour of the Maxilla and Paranasal Sinuses: A Rare Clinical Presentation |
title_full |
Peripheral Primitive Neuroectodermal Tumour of the Maxilla and Paranasal Sinuses: A Rare Clinical Presentation |
title_fullStr |
Peripheral Primitive Neuroectodermal Tumour of the Maxilla and Paranasal Sinuses: A Rare Clinical Presentation |
title_full_unstemmed |
Peripheral Primitive Neuroectodermal Tumour of the Maxilla and Paranasal Sinuses: A Rare Clinical Presentation |
title_sort |
peripheral primitive neuroectodermal tumour of the maxilla and paranasal sinuses: a rare clinical presentation |
publisher |
JCDR Research and Publications Private Limited |
series |
Journal of Clinical and Diagnostic Research |
issn |
2249-782X 0973-709X |
publishDate |
2015-05-01 |
description |
Peripheral Primitive Neuroectodermal Tumours (pPNET) are rare aggressive tumours of neural crest cell origin. These tumours are more
common in children and young adults. This is a unique report of one such presentation in a 23-year-old lady occurring in the left side
posterior maxilla and Paranasal sinuses along with imaging characteristics, histopathologic features, immunohistochemical aspects
and management. Though these tumours are rare, they should be considered in the differential diagnosis of rapidly growing soft tissue
masses in young adults. Precise diagnosis with timely management is necessary for good prognosis.
|
topic |
aggressive oral cavity small round cell tumours |
url |
https://jcdr.net/articles/PDF/5949/13055_CE(RA1)_F(T)_PF1(AGAK)_PFA(AK)_PF2(PAG).pdf |
work_keys_str_mv |
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