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CASE REPORT
Year : 2019  |  Volume : 62  |  Issue : 3  |  Page : 451-453

Nonparameningeal alveolar rhabdomyosarcoma, with cytohistological features: A case report


Department of Pathology and Lab Medicine, Deen Dayal Upadhaya Hospital, Government of NCT, New Delhi, India

Correspondence Address:
Neelam Sood
Deen Dayal Upadhaya Hospital, Government of NCT, New Delhi
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/IJPM.IJPM_471_18

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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.


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