Orbital embryonal rhabdomyosarcoma in association with neurofibromatosis type 1

dc.contributor.author Shome, Debraj
dc.contributor.author Honavar, Santosh G.
dc.contributor.author Reddy, Vijay Anand P.
dc.contributor.author Vemuganti, Geeta K.
dc.date.accessioned 2022-03-27T04:10:49Z
dc.date.available 2022-03-27T04:10:49Z
dc.date.issued 2007-03-01
dc.description.abstract A 20-month-old child with systemic features of neurofibromatosis type 1 presented with sudden-onset proptosis. Biopsy and histopathology confirmed the diagnosis of an embryonal rhabdomyosarcoma. The tumor regressed completely with chemotherapy and external beam radiotherapy. This case highlights the association of rhabdomyosarcoma with neurofibromatosis type 1. ©2007The American Society of Opthalmic Plastic and Reconstructive Surgery, Inc.
dc.identifier.citation Ophthalmic Plastic and Reconstructive Surgery. v.23(2)
dc.identifier.issn 07409303
dc.identifier.uri 10.1097/IOP.0b013e318032af94
dc.identifier.uri https://journals.lww.com/00002341-200703000-00016
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/6599
dc.title Orbital embryonal rhabdomyosarcoma in association with neurofibromatosis type 1
dc.type Journal. Article
dspace.entity.type
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