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Lee et al.
Visual Defects Noted on MRI Examination of Patients With
Pituitary Adenomas
W
Institutions, 600 N Wolfe St, Phipps B100F, Baltimore, hen most neuroradiologists con- ningiomas, craniopharyngiomas, and aneu-
MD 21287. Address correspondence to D. M. Yousem sider the visual field (VF) deficits rysms [2, 3].
(dyousem1@jhu.edu). associated with pituitary adeno- The visual deficits associated with pitu-
2 mas that compress the chiasm, itary adenoma depend on the size, location,
Department of Radiology, Chungnam National University
Hospital, Daejeon, Korea. they automatically think of bitemporal hemi- and hormonal activity of the tumor as well as
anopsia (BHA). This is a VF deficit in which the position of the chiasm as it relates to the
3
Wilmer Eye Institute, The Johns Hopkins Medical all the vision in the temporal fields of both sella turcica [4]. According to a recent study,
Institutions, Baltimore, MD. eyes is lost, leaving only the nasal fields to the tumor volume also affects the severity of
4
Genometrics Section, Computational and Statistical
be perceived. Incomplete bitemporal VF de- the VF defect [5, 6].
Genomics Branch, National Human Genome Research fects are much more common than true Although a previous study of 50 patients
Institute, National Institutes of Health, Baltimore, MD. hemianopsia and are considered by neuro- showed a significant correlation between chi-
WEB ophthalmologists as a sign characteristic of asmal compression and visual disturbances
This is a web exclusive article. chiasmal syndrome, which is usually caused [7], to our knowledge, no MRI-based lit-
by lesions that affect the optic chiasm from erature shows the relationship between the
AJR 2015; 205:W512W518
below [1]. Pituitary adenomas are the most degree and symmetry of extrinsic anteri-
0361803X/15/2055W512 common of all chiasmal syndrome tumors, or visual pathway compression by pituitary
followed by other lesions that cause extrin- macroadenoma and the pattern of VF defects
American Roentgen Ray Society sic optic chiasm compression, such as me- observed in patients. One goal of this study
was to test the hypothesis that bitemporal nosed when the defect affected the entire outer (or as no contact, abutment but not displacement, mild
VF defects, not BHA, are the most common lateral) half of the VF in each eye. displacement (<3 mm of displacement), or moder-
defect in patients with pituitary macroad- A bitemporal defect was diagnosed when the ate displacement ( 3 mm of displacement) (Fig.
enoma. We also wished to determine what defect affected the outer (or lateral) half of the 1). We selected the maximum displacement when
degree of optic chiasm compression is nec- VF in each eye, whereas a mixed defect was diag- more than two parts of the optic pathway were dis-
essary to produce such defects and how of- nosed when the defect involved not only the out- placed by the pituitary macroadenoma.
ten asymmetric visual defects are associated er (or lateral) half of the VF of both eyes but also Two neuroradiologists (one with 8 years of ex-
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with pituitary macroadenoma that asymmet- other areas of the VF in one or both eyes. A mon- perience and one with 3 years of experience) inde-
rically affects the prechiasmal optic nerves, ocular defect was defined as the presence of any pendently measured displacement with the use of
optic chiasm, or postchiasmal optic tracts. VF defect in one eye and a normal VF in the other electronic calipers. The mean of the two recorded
eye. A homonymous defect was defined as a de- displacements was used, unless there was a discrep-
Materials and Methods fect that was present in the temporal (outer) field ancy of more than 3 mm, in which case an adjudica-
This retrospective study was reviewed and ap- of one eye and the nasal (inner) field of the other tion was performed by a third neuroradiologist (with
proved by the institutional review board of The eye and, for the purpose of this study, was thought 25 years of experience), who was blinded to the
Johns Hopkins University School of Medicine. to be consistent with a compressive lesion in the measurements of the other two neuroradiologists.
Because of the retrospective nature of the study, region of the chiasm. Nonspecific defects were de- Asymmetry from right to left in the degree of
informed consent was not required for review of fined as defects that could not clearly be attributed compression of the optic pathway on MRI was
either the medical records or the MR images. to a particular ocular or neurologic process. The evaluated subjectively (Fig. 2). Adjudication was
We retrospectively searched our imaging ar- other category identified defects that the evalu- performed in the same manner as it was for dis-
chive for patients who had pituitary macroadeno- ators thought were not likely caused by the tumor. placement. We also recorded changes in signal in-
ma diagnosed by MRI between November 2009 Finally, unreliable test results were defined as re- tensity on T2-weighted or FLAIR sequences, con-
and October 2012. In all patients, at least one di- sults associated with excessive false-positive re- trast enhancement, and atrophy anywhere along
mension of the pituitary macroadenoma measured sponses, false-negative responses, or fixation loss- the optic pathway and determined the presence of
at least 10 mm. We then reviewed the imaging es still requiring interpretation. hemorrhage in the pituitary lesions.
findings and medical records of the 185 patients Qualitative analysis of the degree of asym- The imaging parameters used for the sagit-
who were identified using this strategy. Sixty-six metry in VF loss between the right and left eyes tal thin T1-weighted sequence were as follows:
patients were excluded either because they did not was also performed for patients with bitemporal, TR/TE, 450/9.5; matrix, 256 256; FOV, 150
have any VF testing results available or because mixed, or homonymous defects. The scale used 150 mm; and section thickness, 2 mm. The coro-
they had other underlying diseases, such as stroke, in such analysis included the following categories nal thin T1-weighted sequence was obtained us-
glaucoma, ocular or intracranial trauma, retinal of asymmetry: significantly more left, somewhat ing the following parameters: TR/TE, 450/9.5;
artery occlusion, other retinal diseases, amblyo- more left, symmetric, somewhat more right, and matrix, 256 256; FOV, 150 150 mm; and sec-
pia, or unrelated optic neuropathy, all of which significantly more right. tion thickness, 2 mm. The parameters used to ob-
could affect the results of VF testing. Next, we re- The four patients who were found to have un- tain the axial T2-weighted sequence were TR/TE,
viewed the clinical findings and ophthalmologic reliable results of VF testing or who received a di- 4050/89; matrix, 384 384; FOV, 220 220 mm;
records of the remaining 119 patients who were agnosis consistent with other ocular or neurologic and section thickness, 4 mm. FLAIR sequence pa-
included in the study, including documentation of diseases were excluded from further analysis. rameters were as follows: TR/TE, 9000/105; in-
VF defects and reported visual complaints. version time, 2500 ms; matrix, 320 320; FOV,
All VF tests were performed using a Humphrey Analysis of MR Images 230 230 mm; and section thickness, 4 mm.
Field Analyzer (Carl Zeiss Meditec). Test patterns Each patient underwent an MRI examination The contrast-enhanced thin coronal T1-weighted
were either 242 or 302, and strategies included that consisted of a standard protocol of sagittal and sequence was obtained using the following param-
use of the Swedish interactive threshold algorithm coronal T1-weighted and CISS/FIESTA (construc- eters: TR/TE, 500/9.5; matrix, 256 256; FOV,
or full threshold. tive interference in steady statefast imaging em- 150 150 mm; and section thickness, 2 mm. The
ploying steady-state acquisition) sequences per- contrast-enhanced thin sagittal T1-weighted se-
Qualitative Visual Field Analysis formed before and after gadolinium contrast agent quence was obtained with the use of the param-
Qualitative analysis of the VF tests was per- administration. All sections were 3 mm or thinner. eters TR/TE, 450/9.4; matrix, 256 256; FOV,
formed by two experienced ophthalmologists (one We evaluated the degree of displacement of the 150 150 mm; and section thickness, 2 mm. The
with 10 years of experience and one with 40 years of prechiasmal optic nerve, optic chiasm, and postchi- parameters used to obtain the contrast-enhanced
experience) who were blinded to the MRI findings. asmal optic tract by the pituitary macroadenoma. If axial T1-weighted sequence were TR/TE, 550/12;
After assessments were performed independently, there was symmetric displacement, we determined matrix, 320 320; FOV, 220 220 mm; and sec-
the analyses were compared jointly, and any differ- the degree of displacement relative to the expected tion thickness, 4 mm. The contrast-enhanced cor-
ences in grading were adjudicated by consensus. normal location of the visual pathway. If there was onal T1-weighted sequence was obtained using
VF test findings were classified as normal (i.e., bilateral but asymmetric displacement, we com- the following parameters: TR/TE, 650/9.1; ma-
no defect), unreliable, or as one of the following pared the displacement on each side with the ex- trix, 320 320; FOV, 230 230 mm; and section
types of defect: bitemporal (bitemporal defect pected location of the visual apparatus. Finally, if thickness, 4 mm.
only, including BHA), mixed (bitemporal and ad- there was unilateral displacement, we determined
ditional defects), monocular, homonymous, non- the displacement of the affected side relative to the Results
specific, or other. BHA, which was included as position of the unaffected side. In all cases, the de- Of the 115 patients (49 women and 66 men;
one type of a bitemporal field defect, was diag- gree of optic pathway displacement was classified mean [SD] age, 54.7 6.2 years; age range,
Asymptomatic Subjects
Sixty-three patients had no visual com-
plaints at presentation; in 14 of these pa-
tients (22.2%), the tumors had no contact
with the optic pathway. In the remainder
of the patients, tumor contact with the op-
tic pathway was as follows: four patients
(6.3%) had tumor abutment but no dis-
placement, 20 (31.7%) had mild displace-
ment, and 25 (39.7%) had moderate dis-
placement. The formal VF test findings for
these asymptomatic patients were classified
as follows: 18 patients (28.6%) had normal
findings, 14 (22.2%) had bitemporal defects
(without BHA), six (9.5%) had mixed de-
fects, one (1.6%) had homonymous defects,
eight (12.7%) had monocular defects, and 16
(25.4%) had nonspecific defects (Fig. 6).
A B
Symptomatic Subjects
Fig. 2MRI classification of asymmetry in the degree of compression in the optic pathway in patients with Fifty-two patients had visual complaints at
pituitary macroadenoma. presentation; in nine of these patients (17.3%),
A, MR image shows asymmetric displacement of right visual field of optic pathway caused by compression by
pituitary macroadenoma.
the tumor had no contact with the optic path-
B, MR image shows asymmetric displacement of optic pathway caused by compression by pituitary way. In the remainder of the patients, tumor
macroadenoma. contact with the optic pathway was as fol-
Patients (no.)
phy of the optic chiasm, and 19 (16.5%) had Normal
hemorrhage. With the exception of one pa- 15 Nonspecific defects
Discussion
Fig. 6Graph showing relationship between displacement of optic pathway and visual fields in 63 patients
Our study confirms that the classic find- without visual complaints.
ing of pure BHA in patients with pituitary
macroadenoma is a myth; only one of the
115 patients in our cohort had this defect. In
fact, the VF defects in our patients with pi- 35
tuitary macroadenoma were purely bitempo-
ral (even if incomplete) in only 29 of 115 pa- 30
20 Normal
ings are comparable to those of other neu-
Nonspecific defects
roophthalmologic studies, which found that Monocular defects
15
pure BHAs are rare compared with bitempo- Homonymous defects
Bitemporal or misdefects
ral defects, with the former occurring in only 10
approximately 1% of patients with pituitary
macroadenoma [1, 8, 9]. 5
We also found that patients with macroad-
enoma may have other defects, including 0
monocular or homonymous defects [5, 10 Moderate Mild Abutting No Contact
Displacement Displacement
12]. Indeed, 40 of the 89 patients with VF de-
fects (44.9%) had nontemporal defects. This Tumor Contact With Optic Pathway
may have resulted from compression of pre-
chiasmal optic nerves or postchiasmal tracts. Fig. 7Graph showing relationship between displacement of optic pathway and visual fields in 52 patients
Involvement of prechiasmal optic nerves or with visual complaints.
postchiasmal tracts was seen in 82 and 21 pa-
tients, respectively. Of the patients with pre- placement noted, with 71% of patients with abnormal VFs in patients who have pituitary
and postchiasmal compression, 79 also had VF defects having moderate optic pathway tumors that do not appear to be in contact
optic chiasm compression. Only nine patients displacement that ranged from 4 to 21 mm. with the optic apparatus may be attributed
had pure optic chiasm compression alone. Eight patients in this study had abnormal to previous indentation (and subsequent tu-
Thus, it is more common to have extrachias- VFs, a finding that was thought to be con- mor regression), hormonal influences, intra-
mal optic pathway involvement along with sistent with optic pathway damage resulting tumor hemorrhage, autonecrosis, or vascu-
compression of the chiasm, rather than just from their tumors, although MRI examina- lar shunting [13]. In our study, the smallest
chiasm compression alone. Previous studies tion of these patients revealed no contact be- displacement of the optic apparatus from its
did not evaluate extrachiasmal compression, tween the tumor and the optic apparatus. It expected normal position in a patient with
evaluating only chiasmal compression instead. is possible that in some of these patients, the a presumed related VF defect was 4 mm on
In general, VF defects (whether bitempo- VF defect was spurious or related to a proc- the coronal plane, compared with previous
ral, mixed, homonymous, or monocular) cor- ess other than the tumor. Alternatively, some reports indicating a minimum displacement
related with the degree of optic pathway dis- studies have theorized that the discovery of of 1213 mm [7, 9]. This discrepancy may
Patients (no.)
Ophthalmol 2003; 14:325331 PJ, Danesh-Meyer HV. Visual acuity and pattern manifesting as homonymous hemianopia. Jpn J
3. Jacobs DA, Galetta SL. Neuro-ophthalmology for of visual field loss at presentation in pituitary ad- Ophthalmol 2007; 51:151153
neuroradiologists. AJNR 2007; 28:38 enoma. JClin Neurosci 2014; 21:735740 13. Levy A. Pituitary disease: presentation, diagno-
4. Kapoor S. Acromegaly. N Engl J Med 2007; 9. Schmalisch K, Milian M, Schimitzek T, Lagrze sis, and management. JNeurol Neurosurg Psy-
356:12741275 [author reply, 12751276] WA, Honegger J. Predictors for visual dysfunc- chiatry 2004; 75:iii47iii52
5. Lee JP, Park IW, Chung YS. The volume of tumor tion in nonfunctioning pituitary adenomas: impli- 14. Saeki N, Uchino Y, Murai H, et al. MR imaging
mass and visual field defect in patients with pitu- cations for neurosurgical management. Clin En- study of edema-like change along the optic tract
Downloaded from www.ajronline.org by 36.86.56.101 on 04/12/17 from IP address 36.86.56.101. Copyright ARRS. For personal use only; all rights reserved
itary macroadenoma. Korean J Ophthalmol 2011; docrinol (Oxf) 2012; 77:728734 in patients with pituitary region tumors. AJNR
25:3741 10. Hershenfeld SA, Sharpe JA. Monocular temporal 2003; 24:336342
6. Kan E, Kan EK, Atmaca A, Atmaca H, Colak R. hemianopia. BrJ Ophthalmol 1993; 77:424427 15. Poon A, McNeill P, Harper A, ODay J. Patterns
Visual field defects in 23 acromegalic patients. Int 11. Rivoal O, Brzin AP, Feldman-Billard S, Luton of visual loss associated with pituitary macroad-
Ophthalmol 2013; 33:521525 JP. Goldmann perimetry in acromegaly: a survey enomas. Aust N Z J Ophthalmol 1995; 23:107115
7. Ikeda H, Yoshimoto T. Visual disturbances in pa- of 307 cases from 1951 through 1996. Ophthal- 16. Wang X, Neely AJ, McIlwaine GG, Lueck CJ.
tients with pituitary adenoma. Acta Neurol Scand mology 2000; 107:991997 Multi-scale analysis of optic chiasmal compres-
1995; 92:157160 12. Nishimura M, Kurimoto T, Yamagata Y, Ikemoto sion by finite element modelling. J Biomech 2014;
8. Ogra S, Nichols AD, Stylli S, Kaye AH, Savino H, Arita N, Mimura O. Giant pituitary adenoma 47:22922299