Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case report

Rhabdomyosarcoma (RMS) is a tumor arising from primitive mesenchymal cell with tendency for myogenesis. WHO classification categorizes this entity as embryonal, alveolar, spindle cell/sclerosing, and pleomorphic subtypes removing botryoid as a separate entity. The alveolar variant has worse prognosi...

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Main Authors: Neelam Sood, Arun K Haldia
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Indian Journal of Pathology and Microbiology
Subjects:
Online Access:http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2019;volume=62;issue=3;spage=451;epage=453;aulast=Sood
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spelling doaj-b954e96205d847b1bd75a1961f60cf182020-11-24T22:06:25ZengWolters Kluwer Medknow PublicationsIndian Journal of Pathology and Microbiology0377-49292019-01-0162345145310.4103/IJPM.IJPM_471_18Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case reportNeelam SoodArun K HaldiaRhabdomyosarcoma (RMS) is a tumor arising from primitive mesenchymal cell with tendency for myogenesis. WHO classification categorizes this entity as embryonal, alveolar, spindle cell/sclerosing, and pleomorphic subtypes removing botryoid as a separate entity. The alveolar variant has worse prognosis and the cytological features of this entity are similar to embryonal type with little variations. This case report describes the cytohistological features of alveolar RMSfrom a 9-year-old child with nonparameningeal location.http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2019;volume=62;issue=3;spage=451;epage=453;aulast=SoodAlveolarcytohistologic featuresrhabdomyosarcoma
collection DOAJ
language English
format Article
sources DOAJ
author Neelam Sood
Arun K Haldia
spellingShingle Neelam Sood
Arun K Haldia
Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case report
Indian Journal of Pathology and Microbiology
Alveolar
cytohistologic features
rhabdomyosarcoma
author_facet Neelam Sood
Arun K Haldia
author_sort Neelam Sood
title Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case report
title_short Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case report
title_full Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case report
title_fullStr Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case report
title_full_unstemmed Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case report
title_sort nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: a case report
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Pathology and Microbiology
issn 0377-4929
publishDate 2019-01-01
description Rhabdomyosarcoma (RMS) is a tumor arising from primitive mesenchymal cell with tendency for myogenesis. WHO classification categorizes this entity as embryonal, alveolar, spindle cell/sclerosing, and pleomorphic subtypes removing botryoid as a separate entity. The alveolar variant has worse prognosis and the cytological features of this entity are similar to embryonal type with little variations. This case report describes the cytohistological features of alveolar RMSfrom a 9-year-old child with nonparameningeal location.
topic Alveolar
cytohistologic features
rhabdomyosarcoma
url http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2019;volume=62;issue=3;spage=451;epage=453;aulast=Sood
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AT arunkhaldia nonparameningealalveolarrhabdomyosarcomawithcytohistologicalfeaturesacasereport
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