Title of article
Orbital rhabdomyosarcomas: A review
Author/Authors
Jurdy, Lama University of Amsterdam - Academic Medical Center, Orbital Centre - Department of Ophthalmology, Netherlands , Merks, Johanus H.M. University of Amsterdam - Academic Medical Center - Department of Paediatric Oncology, Netherlands , Pieters, Bradly R. University of Amsterdam - Academic Medical Center - Department of Radiotherapy, Netherlands , Mourits, Maarten P. University of Amsterdam - Academic Medical Center, Orbital Centre - Department of Ophthalmology, Netherlands , Kloos, Roel J.H.M. University of Amsterdam - Academic Medical Center, Orbital Centre - Department of Ophthalmology, Netherlands , Strackee, Simone D. University of Amsterdam - Academic Medical Center - Department of Plastic and Reconstructive Surgery, Netherlands , Saeed, Peerooz University of Amsterdam - Academic Medical Center, Orbital Centre - Department of Ophthalmology, Netherlands
From page
167
To page
175
Abstract
Rhabdomyosarcoma (RMS) is a highly malignant tumor and is one of the few life-threatening diseases that present first to the ophthalmologist. It is the most common soft-tissue sarcoma of the head and neck in childhood with 10% of all cases occurring in the orbit. RMS has been reported from birth to the seventh decade, with the majority of cases presenting in early childhood. Survival has changed drastically over the years, from 30% in the 1960’s to 90% presently, with the advent of new diagnostic and therapeutic modalities. The purpose of this review is to provide a general overview of primary orbital RMS derived from a literature search of material published over the last 10 years, as well as to present two representative cases of patients that have been managed at our institute.
Keywords
Rhabdomyosarcoma , Tumor , Orbit , Eye , AMORE , Genetics , Pediatrics , Brachy therapy
Journal title
Saudi Journal of Ophthalmology
Journal title
Saudi Journal of Ophthalmology
Record number
2577571
Link To Document