TY - JOUR
T1 - Repair after xenon arc photocoagulation. 2. A clinical and light microscopic study of the evolution of retinal lesions in the rhesus monkey
AU - Wallow, Ingolf H.L.
AU - Tso, Mark O.M.
N1 - Funding Information:
In addition, to determine whether lesions more severe than those considered "ideal" would also lead to a union between retina and choroid, we produced and followed a second group of more severe burns. These were of a magnitude comparable to those originally recommended for therapeutic use Armed Forces Institute of Pathology, and the Department of Ophthalmology, George Washington University Medical Center, Washington, D.C. This work was supported in part by a research contract, Project Number 38061102B71P-06, from the Medical Research and Development Command, U.S. Army, Washington, D.C, and Public Health Service Grants EY-00397 and EY-00790 (Dr. Tso), and by Trainings Grants Wa 217/1 and 217/2 from the Deutsche Forschungsgemeinschaft (Dr. Wallow).
PY - 1973/4
Y1 - 1973/4
N2 - The evolution of two groups of lesions produced by photocoagulation in the retina of the rhesus monkey was studied by ophthalmoscopy and by light microscopy. In the first group, the moderate lesions were comparable to those that have been considered by Curtin and Norton as "ideal" for the creation of chorioretinal adhesions in human subjects. In the second group, the severe lesions were comparable to lesions that had been proposed by Meyer-Schwickerath as producing chorioretinal adhesions in man. Histopathologically, no adhesions of the retina were observed in the lesions of the first group. Adhesions of the retina did occur in the lesions of the second group, but Bruch's membrane was intact in all lesions, and no direct contribution to these adhesions from the choroid was observed. Thus, these adhesions were not truly chorioretinal. Instead, they appeared to be a union between retinal glial cells and the RPE or between retinal glial cells and Bruch's membrane. Ophthalmoscopically, two types of hyperpigmentation were observed. The first was attributable to accumulations of pigmentladen macrophages. In lesions of moderate severity these macrophages formed a ring around the center, while in severe lesions they were present throughout the central region. The second type of hyperpigmentation was due to the presence of hyperpigmented cells of the RPE around the lesions and was observed in both moderately severe and severe lesions.
AB - The evolution of two groups of lesions produced by photocoagulation in the retina of the rhesus monkey was studied by ophthalmoscopy and by light microscopy. In the first group, the moderate lesions were comparable to those that have been considered by Curtin and Norton as "ideal" for the creation of chorioretinal adhesions in human subjects. In the second group, the severe lesions were comparable to lesions that had been proposed by Meyer-Schwickerath as producing chorioretinal adhesions in man. Histopathologically, no adhesions of the retina were observed in the lesions of the first group. Adhesions of the retina did occur in the lesions of the second group, but Bruch's membrane was intact in all lesions, and no direct contribution to these adhesions from the choroid was observed. Thus, these adhesions were not truly chorioretinal. Instead, they appeared to be a union between retinal glial cells and the RPE or between retinal glial cells and Bruch's membrane. Ophthalmoscopically, two types of hyperpigmentation were observed. The first was attributable to accumulations of pigmentladen macrophages. In lesions of moderate severity these macrophages formed a ring around the center, while in severe lesions they were present throughout the central region. The second type of hyperpigmentation was due to the presence of hyperpigmented cells of the RPE around the lesions and was observed in both moderately severe and severe lesions.
UR - https://www.scopus.com/pages/publications/0015612175
UR - https://www.scopus.com/pages/publications/0015612175#tab=citedBy
U2 - 10.1016/0002-9394(73)90813-1
DO - 10.1016/0002-9394(73)90813-1
M3 - Article
C2 - 4633188
AN - SCOPUS:0015612175
SN - 0002-9394
VL - 75
SP - 610
EP - 626
JO - American journal of ophthalmology
JF - American journal of ophthalmology
IS - 4
ER -