Orbital rhabdomyosarcoma in an adult

Authors

  • P Lavaju Department of Ophthalmology, B.P. Koirala Institute of Health Sciences, Dharan
  • H Das Department of Ophthalmology, B.P. Koirala Institute of Health Sciences, Dharan
  • P Malla Department of Ophthalmology, B.P. Koirala Institute of Health Sciences, Dharan
  • A Tiwari Department of Radiology, B.P. Koirala Institute of Health Sciences, Dharan
  • A Sinha Department of Pathology, B.P. Koirala Institute of Health Sciences, Dharan
  • P Upadhyaya Department of Pathology, B.P. Koirala Institute of Health Sciences, Dharan

DOI:

https://doi.org/10.3126/nepjoph.v2i1.3707

Keywords:

Orbital rhabdomyosarcoma

Abstract

Introduction: Rhabdomyosarcoma is the most common primary orbital malignant tumor in children. Orbital lesions represent about 10 % of all the cases of rhabdomyosarcoma. Rhabdomyosarcoma is a rare cause of proptosis in adults.

Objective: To report a case of primary orbital rhabdomyosarcoma in a 45-year-old female.

Design: Interventional case report. The main outcome measures are a rare cause of proptosis in an adult, discussion on treatment options and prognosis of rhabdomyosarcoma.

Result: The patient underwent total orbital exenteration and was referred for radiotherapy and chemotherapy.

Conclusion: Rhabdomyosarcoma is a rare cause of proptosis in adults. It should be suspected in a case of rapidly-progressive proptosis in adults.

DOI: 10.3126/nepjoph.v2i1.3707

Nep J Oph 2010;2(1) 64-67

Downloads

Download data is not yet available.
Abstract
804
PDF
675

Downloads

How to Cite

Lavaju, P., Das, H., Malla, P., Tiwari, A., Sinha, A., & Upadhyaya, P. (2010). Orbital rhabdomyosarcoma in an adult. Nepalese Journal of Ophthalmology, 2(1), 64–67. https://doi.org/10.3126/nepjoph.v2i1.3707

Issue

Vol. 2 No. 1 (2010)

Section

Case Reports

License

This license enables reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.