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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Main Authors: C.L. Krithika, S. Sathasivasubramanian, C. Ponranjini Vedeswari
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2015-05-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/5949/13055_CE(RA1)_F(T)_PF1(AGAK)_PFA(AK)_PF2(PAG).pdf
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spelling 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
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