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Scholars Journal of Medical Case Reports | Volume-2 | Issue-10
Orbital Rhabdomyosarcoma in a Child
Sailaja Vallury, Kavitha Toopalli, Modini Pandharpurkar
Published: Oct. 29, 2014 |
188
220
DOI: 10.36347/sjmcr.2014.v02i10.010
Pages: 674-676
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Abstract
Rhabdomyosarcoma(RMS) is the most common soft tissue sarcoma in children and frequently involves the
head and neck region with 10% of the cases primarily involving the orbit. It is a highly malignant tumor which can be
life threatening. CT and MRI are important in the evaluation of this tumor. Histologically, embryonal subtype is the
commonest in children. Complete resection followed by chemotherapy and radiotherapy is the preferred treatment of
choice. We report a case of Embryonal Rhabdomyosarcoma of Orbit presenting with rapid proptosis of right eye in a 13
year old female child.