CLINICOPATHOLOGICAL CORRELATION OF ARGON-LASER PHOTOCOAGULATION OF RETINAL ANGIOMAS IN A PATIENT WITH VONHIPPEL-LINDAU DISEASE FOLLOWED FORMORE THAN 20 YEARS
Rh. Rosa et al., CLINICOPATHOLOGICAL CORRELATION OF ARGON-LASER PHOTOCOAGULATION OF RETINAL ANGIOMAS IN A PATIENT WITH VONHIPPEL-LINDAU DISEASE FOLLOWED FORMORE THAN 20 YEARS, Retina, 16(2), 1996, pp. 145-156
Purpose: The authors review the histopathologic findings in the eyes o
f a patient with multiple retinal angiomas and von Hippel-Lindau disea
se, who underwent treatment with argon laser photocoagulation with fol
low-up of more than 20 years. Methods: The patient was studied ophthal
moscopically and by fluorescein angiography before and after argon las
er photocoagulation of retinal angiomas. The eyes were obtained postmo
rtem, and the central portion of the right eye, including the macula a
nd optic nerve head, was sectioned serially for light microscopy. The
pupil-optic nerve segment of the left eye was step-sectioned serially
for light microscopy. Results: Histopathologic study of the right eye
disclosed mild cystoid macular edema and focal areas of exudation in t
he midperiphery possibly secondary to irradiation of the head. A 1.5 x
0.3-mm area of residual angioma was present in the nasal peripapillar
y retina. Superotemporally, four chorioretinal scars were present in o
ne photocoagulated area. These scars were composed of dense fibrous ti
ssue with vascularization and variable retinal pigment epithelium hype
rplasia. Large, nonangiomatous vessels within each of the scars were c
ontinuous with other retinal vessels. Inferotemporally, two chorioreti
nal scars were present in one photocoagulated area. Histopathologicall
y, these scars were similar to the superotemporal scars, except that n
o patent retinal vessels traversed the inferotemporal scars. Neovascul
arization of the retina was associated with one superotemporal and one
inferotemporal scar. No residual angiomatous tissue was present in th
e supero- or inferotemporal areas. Histopathologic examination of the
left eye disclosed extensive vitreous organization and periretinal fib
rovascular proliferation, extensive gliosis of the retina, and a 4.5 X
2-mm schisis cavity filled with fibrinous exudate. Three angiomas wit
h variable fibrosis were present in the left eye. Conclusion: Despite
a poor clinical course in one eye treated with xenon are photocoagulat
ion, trans-scleral diathermy, and argon laser photocoagulation, a pati
ent with von Hippel-Lindau disease and multiple retinal angiomas retai
ned good vision in the other eye after successful treatment with argon
laser photocoagulation with follow-up of more than 20 years, The amou
nt of regression of angiomatous tissue after photocoagulation varied f
rom lesion to lesion (complete in some; minimal in others). The author
s conclude that argon laser photocoagulation of early lesions is effec
tive in ablating smaller (less than or equal to 3-disc diameter) retin
al angiomas.