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AIiOzgen’ OBJECTIVE. The purposes of this study were to establish criteria for the diameters of nor-
mal extraocular muscles, to determine the normal position of the globe as revealed by CT. and to
Macit Ariyurek
investigate the effects of age and sex on these structures.
SUBJECTS AND METHODS. Diameters of extraocular muscles, distance from the in-
terzygomatic line to the posterior margin of the globe. width of the optic nerve-sheath com-
plex. and length of the interzygomatic line were calculated for 2(X) normal orbits of 100
American Journal of Roentgenology 1998.170:1093-1096.
patients on axial and direct coronal CT images. Effects of age and sex on muscle diameters and
globe position were analyzed.
RESULTS. Normal ranges for the diameters (mean ± 2SDs) of extraocular muscles were
medial rectus. 3.3-5.0 mm: lateral rectus, I .7-4.8 mm: inferior rectus. 3.2-6.5 mm; and superior
group. 3.2-6. 1 mm. The normal position of the globe was 9.4 mm behind the interzygomatic
line (range. 5.9-l2. mm). The mean diameters ofthe extraocular muscles and the length of the
interzygomatic line in male patients were significantly larger than in female patients (p < .()0l).
Statistically significant correlation was found between age and the diameters of the inferior and
lateral rectus muscles(r= .32.p = .013: and r= .23.p = .048. respectively).
CONCLUSION. Our results may be important in interpreting CT scans of the orbit be-
cause. tO our knowledge. no reliable normative data exist regarding these orbital structures.
C T has
nique
become
for
a widely
imaging of
used
the
tech-
orbit
were
ditions
clinical suspicion
of the paranasal
of tumor
sinuses
and tumorlike
fr which
con-
surgical
since the l970s. Although normal treatment was contemplated. All patients in this
study were free ofclinical evidence or history of en-
anatomy of the orbital structures as seen on
docrine disease or any orbital disorder. Asymmetric
CT is described in many references. in a re-
scans. scans with artifacts for any reason (dental
view of the literature we could not find reli-
material. eye motion. etc. ) that may cause errors in
able quantitative normative CT data for orbit measurements. and CT scans with abnormal
extraocular muscle diameters, which may be orbital findings were excluded. Two hundred nor-
important in evaluating an individual with mal orbits of 1(X) patients (44 men and 56 women)
suspected orbital disease such as Graves’ orb- were evaluated in this study. The age range of the
itopathy. In this situation. the ranges of diame- patients was 18-70 years (mean. 4 I years).
tens of healthy extraocular muscles may be
critical to accurately assess the muscles as Methods
normal. The same information is needed to di- Both axial and direct coronal, 3-mm-thick non-
Fig. 2.-Sequential coronal CT scans of 23-year-old woman with sinusitis. Black lines indicate maximum diameters of muscles, where measurements were made.
A-C, Scans show measurement of superior muscle group (A), medial rectus muscle (B), and inferior and lateral rectus muscles (C).
Medial rectus 4.2 3.3-5.0 0.5 avoid dental amalgams or because of limita-
Lateral nectus 3.3 1.7-4.8 0.7 tions in neck mobility in both groups. The
window level and width settings of that study
Superior group 4.6 3.2-6.1 0.9
(70 and 350 H, respectively) were also differ-
Inferior rectus 4.8 3.2-6.5 1.1
ent from our settings. Data for the lateral nec-
Sum of all muscles 16.9 13.1-20.7 1.4
tus muscle. the superior muscle group. and the
Globe positionb 9.4 5.9-12.8 1.0
sum of all muscles were significantly smaller
Optic nerve-sheath complex 4.4 3.2-5.6 0.7
in that study than in ours.
lnterzygomatic line 99 91-108 Some volumetric studies in patients with
Note-Medial and lateral rectus muscles were measured on axial plane, and superior group and inferior rectus muscle were Graves’ disease were also published. but the
measured on coronal plane at window level and width settings of 50 and 250 H, respectively. The diameter of each muscle was
volumetric method of quantitative evaluation
measured at its maximum.
aDifference range between right and left orbit data in 95th percentile limits. of the extraocular muscle volumes is time-
bperpendicular distance between interzygomatic line and posterior margin ofthe globe. consuming and needs additional specific hard-
ware and software I 10. 1 1 J. These volumetric
We found no consistent correlation between muscles are imaged for these reasons on CT studies also lack a sufficient number of control
age and the width of the optic nerve-sheath and evaluated qualitatively and subjectively
American Journal of Roentgenology 1998.170:1093-1096.
positively correlated with the diameter of each would be valid for specific window level and dardized A-scan echography and computerized to-
muscle, and the mean length of the interzygo- width settings, 50 and 250 H, respectively. mography scan measurements. Ophthalmology
1985:92:1351-1355
matic line in male patients is also significantly In conclusion, we present normal orbital
7. Barrett L. Glatt Hi. Burde RM. Gado MH. Optic
more than in female patients, whereas the ra- measurements that may help observers to ac-
nerve dysfunction in thyroid eye disease. Radio!-
tio of the length of the interzygomatic line to curately assess enlargement or atrophy of ex- og\, 1988:167:503-507
the diameter of each muscle does not show a traocular muscles and to determine whether 8. Jacobs L. Weisberg LA, Kinkel WR. Computerized
statistically significant difference between exophthalmos (or enophthalmos) is present in tomography (1 the orbit and se!!a turn’ica. New
male and female patients. We think that the a practical quantitative method. Because the York: Raven. 1980:27-85
9. Nugent RA. Belkin RI, Neigel JM, et al. Graves
difference between the diameters of extraocu- normative data for any sex (Table 2) show
orbitopathy: correlation of CT and clinical find-
lar muscles in men and women depends on equal to or less than 8% difference from the
ings. Radiology 1990;177:675-682
the head size (which may be represented by normative data for the population (Table I),
10. Forbes G, Gorman CA, Gehring D. Baker HL.
the length of the interzygomatic line) rather the latter may be used as the normative data Computer analysis of orbit fat and muscle volumes
than the sex of the patient. for all patients in a more practical method, al- in Graves ophthalmopathy. AJNR 1983:4:737-740
The sum of the diameters of all extraocu- though normal values for each sex may pro- 1 1. Forbes G. Gorman CA. Brennan MD, Gehring DO,
lar muscles may help as an overall index to vide slightly more accurate determination. Ilstnip DM, Earnest F. Ophthalmopathy of Graves’
disease: computerized volume measurements of the
evaluate patients’ measurements, particularly
orbit fat and muscle. AJNR 1986;7:65l-656
in patients with Graves’ disease, in which the References 12. Hallin ES. Feldon SE. Graves’ ophthalmopathy. 1.
diameter of an individual muscle remains in 1. Trokel SL, Hilal SK. Recognition and differential di- Simple CT estimates of extraocular muscle vol-
the normal range although the muscle is ac- agnosis ofenlagod extraocular muscles in computed ume. BrJ Ophthaltnol 1988:72:674-677
tually minimally enlarged. Values for the tomography.Am J Op/u/ia/mo! 197987:503-5l2 13. Chen YL, Chang TC. Huang KM. Tzeng SS. Kao
limits of the differences between diameters 2. Rothfus WE. Curtin HD. Extraocular muscle en- SCS. Relationship of eye movement to computed
American Journal of Roentgenology 1998.170:1093-1096.
largement: CT review. Radiology 198.3;l5l:677-681 tomographic findings in patients with Graves oph-
of healthy contralateral extraocular muscles
3. Patrinely JR. Osbom AG. Anderson RL. Whiting thalmopathy. Ac’ta Ophthalmo! 1994:72:472-477
may also be helpful.
AS. Computed tomographic features of nonthyroid 14. Wilson RG. Pope RM, Michell Mi, Cannon R,
Some researchers evaluated diameters of extraocular muscle enlargement. Ophthalmology McGregor AM. The use of real-time ultrasound in
extraocular muscles with varying window set- 1989;96:l038-l047 Graves’ ophthalmopathy: a comparison with corn-
tings [12, 13, 16]. Every change in the win- 4. Yoshikawa K, Higashide 1, Nahase Y, Inoue 1, In- puted tomography. BrJ Radio! 1989:62:705-709
dow level and width settings results in oue Y, Shiga H. Role of rectus muscle enlargement 15. Unsold R. Newton TH. De Groot I. CF evaluation
different values with respect to the muscle in clinical profile of dysthyroid ophthalmopathy. of extraocular muscles: anatomic-CT correlations.
Jpn J Ophthalmol 1991;35:175-l8l Aibrechi Von Graefes Arch KIm Ophthalmo! 1980;
size. That means that window settings should
5. Hudson HL, Levin L, Feldon SE. Graves exoph- 214: 155-180
be the same to accurately compare the muscle
thalmos unrelated to extraocular muscle enlarge- 16. Feldon SE. Levin L. Liu 5K. Graves’ ophthalmopa-
sizes both between different patients and be- ment. Ophthalmology 1991;98:1495-l499 thy: correlation of saccadic eye movements with age.
tween different CT examinations of the same 6. Holt JE. O’Connor PS, Douglas JP. Byrne B. presence ofoptic neuropathy. and extnaocular muscle
patient. For this reason, our normative data Extraocular muscle size comparison using stan- volume. An’h Ophtha!mo! 1990:l08:1568-l57l