We reviewed computed tomography (CT) studies in 30 patients with histo
logically confirmed orbital rhabdomyosarcoma. There were 17 male and 1
3 female patients, mean age 8.8 years (median age 7 years, age range 1
month to 51 years). The tumour occupied the intra and extraconal comp
artments in 14 (47%) cases; it was solely extraconal in 11 (37%) and i
ntraconal in five (16%), Within the orbit the upper inner quadrant was
the most common site, 20 (67%) of the tumours lying in this region. M
ore than one quadrant was involved in 16 (53%) cases. The epicentre of
the tumour was in the eyelids of three (10%) patients. At presentatio
n the mean size of the mass was 25 x 17 mm in long and short axis diam
eters, respectively. The tumours were of soft tissue density with mode
rately well defined margins and an irregular shape. They showed mild t
o moderate contrast enhancement, Calcification was seen in one case. C
hanges in the adjacent bone were seen in at least 12 (40%) patients. I
ntracranial extension was present in one (3%) patient and invasion of
the paranasal sinuses was also seen in one (3%) patient. The intraorbi
tal structures were displaced or encased by the tumour mass. The globe
was displaced and distorted but not invaded by the tumour. Magnetic r
esonance imaging (MRI) studies were also reviewed in five patients, On
T1-weighted images the tumour gave a similar signal to muscle but on
T2-weighted images it gave a higher signal.