TY - JOUR
T1 - Traumatic enucleation for posterior uveal melanoma
AU - Specht, C. S.
AU - McLean, I. W.
AU - Biscoe, B. W.
N1 - Funding Information:
From the Department of Ophthalmic Pathology and the Registry of Ophthalmic Pathology, Armed Forces Institute of Pathology, Washington, D.C. This study was supported in part by research grant EY04482 from the National Eye Institute.
PY - 1990
Y1 - 1990
N2 - Two features of eyes enucleated for posterior uveal melanoma that may serve as indicators for traumatic enucleation and relate to dissemination of tumor cells at the time of enucleation are myelin artifact of the optic nerve head and acute hemorrhage within the tumor. Myelin artifact occurs when crushed optic nerve tissue is squeezed into the eye at the time of enucleation. Intralesional hemorrhage may occur during surgery and may be correlated with fluctuations in intraocular pressure. We reviewed 519 cases of posterior uveal melanoma treated by enucleation between 1950 and 1970. Without knowledge of the follow-up data, we examined histologic sections for myelin artifact, intralesional hemorrhage, subretinal hemorrhage, Callender cell type, size of tumor, necrosis, and scleral or orbital invasion. Neither myelin artifact nor intralesional hemorrhage were independent prognostic risk factors. These findings do not support or refute the hypothesis that excessive trauma during enucleation results in a worse prognosis.
AB - Two features of eyes enucleated for posterior uveal melanoma that may serve as indicators for traumatic enucleation and relate to dissemination of tumor cells at the time of enucleation are myelin artifact of the optic nerve head and acute hemorrhage within the tumor. Myelin artifact occurs when crushed optic nerve tissue is squeezed into the eye at the time of enucleation. Intralesional hemorrhage may occur during surgery and may be correlated with fluctuations in intraocular pressure. We reviewed 519 cases of posterior uveal melanoma treated by enucleation between 1950 and 1970. Without knowledge of the follow-up data, we examined histologic sections for myelin artifact, intralesional hemorrhage, subretinal hemorrhage, Callender cell type, size of tumor, necrosis, and scleral or orbital invasion. Neither myelin artifact nor intralesional hemorrhage were independent prognostic risk factors. These findings do not support or refute the hypothesis that excessive trauma during enucleation results in a worse prognosis.
UR - http://www.scopus.com/inward/record.url?scp=0025066276&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025066276&partnerID=8YFLogxK
U2 - 10.1016/S0002-9394(14)77875-4
DO - 10.1016/S0002-9394(14)77875-4
M3 - Article
C2 - 2240138
AN - SCOPUS:0025066276
SN - 0002-9394
VL - 110
SP - 518
EP - 521
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
IS - 5
ER -