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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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 |
work_keys_str_mv |
AT neelamsood nonparameningealalveolarrhabdomyosarcomawithcytohistologicalfeaturesacasereport AT arunkhaldia nonparameningealalveolarrhabdomyosarcomawithcytohistologicalfeaturesacasereport |
_version_ |
1725823921805066240 |