TY - JOUR
T1 - Optical Coherence Tomography
T2 - Pathology Correlation of Optic Disc Melanocytoma
AU - Finger, Paul T.
AU - Natesh, Sribhargava
AU - Milman, Tatyana
N1 - Funding Information:
Supported by The EyeCare Foundation, Inc.; and a grant from John and Myrna Daniels, Toronto, Canada, New York, New York, and Palm Beach, FL. Dr Sribhargava Natesh was supported by a Fellowship Grant from the International Federation of Ophthalmological Societies–International Council of Ophthalmology, San Francisco, CA. Dr Milman was supported by the New York Eye and Ear Infirmary Research Fund, New York, New York.
PY - 2010/1
Y1 - 2010/1
N2 - Objective: To correlate combined optical coherence tomography (OCT) and scanning laser ophthalmoscope (SLO) imaging to clinical and histopathologic characteristics of optic disc melanocytoma (ODM). Design: Retrospective, consecutive clinical case analysis. Participants: Twenty patients with ODM were evaluated. Testing: All underwent ophthalmic examinations including a best-corrected visual acuity, slit-lamp examination, dilated ophthalmoscopy, fundus photography with angiography, B-scan ultrasonography, and combined OCT and SLO imaging. Main Outcome Measures: One eye, treated by enucleation, was evaluated by pathologic analysis and was correlated to its combined OCT and SLO images. These findings were correlated to clinical and OCT information from 19 patients with ODM. Results: Histopathologic and combined OCT and SLO features included: disruption of the internal limiting membrane, disorganization of the retina (overlying the tumor), and visualization of the tumor's subretinal surface. Compressive and infiltrative changes in the optic nerve, peripapillary choroid, and retina were correlated directly to combined OCT and SLO images. To varying degrees, these histopathologic findings were seen on combined OCT and SLO. However, the pigment of the ODMs blocked OCT reflectance deep to the tumor's surface. Conclusions: This study demonstrated that OCT and SLO findings could be correlated directly with histopathologic characteristics. Imaging with OCT can be used to diagnose and correlate secondary retinal, superficial, and subretinal tumor characteristics. Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.
AB - Objective: To correlate combined optical coherence tomography (OCT) and scanning laser ophthalmoscope (SLO) imaging to clinical and histopathologic characteristics of optic disc melanocytoma (ODM). Design: Retrospective, consecutive clinical case analysis. Participants: Twenty patients with ODM were evaluated. Testing: All underwent ophthalmic examinations including a best-corrected visual acuity, slit-lamp examination, dilated ophthalmoscopy, fundus photography with angiography, B-scan ultrasonography, and combined OCT and SLO imaging. Main Outcome Measures: One eye, treated by enucleation, was evaluated by pathologic analysis and was correlated to its combined OCT and SLO images. These findings were correlated to clinical and OCT information from 19 patients with ODM. Results: Histopathologic and combined OCT and SLO features included: disruption of the internal limiting membrane, disorganization of the retina (overlying the tumor), and visualization of the tumor's subretinal surface. Compressive and infiltrative changes in the optic nerve, peripapillary choroid, and retina were correlated directly to combined OCT and SLO images. To varying degrees, these histopathologic findings were seen on combined OCT and SLO. However, the pigment of the ODMs blocked OCT reflectance deep to the tumor's surface. Conclusions: This study demonstrated that OCT and SLO findings could be correlated directly with histopathologic characteristics. Imaging with OCT can be used to diagnose and correlate secondary retinal, superficial, and subretinal tumor characteristics. Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.
UR - http://www.scopus.com/inward/record.url?scp=72749113279&partnerID=8YFLogxK
U2 - 10.1016/j.ophtha.2009.06.015
DO - 10.1016/j.ophtha.2009.06.015
M3 - Article
C2 - 19815289
AN - SCOPUS:72749113279
SN - 0161-6420
VL - 117
SP - 114
EP - 119
JO - Ophthalmology
JF - Ophthalmology
IS - 1
ER -