Different approaches treat complications of vasoproliferative tumors
Though the small tumors are themselves benign, they are frequently associated with vision-threatening complications.
TAORMINA, Italy — Skill in diagnosis and the right choice of single or combined treatment are crucial to preserving vision with complications of vasoproliferative retinal tumors. Proper diagnosis and treatment can guarantee satisfactory functional results in most cases, according to Javier Elizalde, MD, of the Barraquer Ophthalmic Center in Barcelona, Spain.
Vasoproliferative retinal tumors are benign and relatively small in size, but they may often be the cause of vitreoretinal complications profoundly impairing visual acuity. At the Jules Gonin Club meeting here, Dr. Elizalde presented a series of cases in which different therapeutic methods were successfully applied.
---Peripheral vasoproliferative tumor associated to Coats’ syndrome with secondary lipid exudation within the macula. Coats’ disease may reveal varying degrees of vascular malformations, including telangiectasis, aneurysms and these unusual exudative peripheral tumors that might be mistaken for a retinal capillary hemangioma.
He introduced his study by explaining that vasoproliferative retinal tumors are intraocular masses composed predominantly of vascular and glial tissue. These lesions were first described as “presumed acquired retinal hemangiomas,” and in 1995 they were reclassified by Carol Shields as “vasoproliferative tumors of the ocular fundus.” Fiona Irvine and coauthors recently suggested the term “reactionary retinal glioangiosis” based on histopathologic observations of the lesions. The tumor appears as a reactive mass containing blood vessels that may derive from sensory retina and possibly from glial cells or retinal pigment epithelial cells.
“Most of the vasoproliferative tumors are solitary and are typically located in the inferior, inferotemporal, or temporal region of the fundus,” Dr. Elizalde explained. “Clinical features of these lesions vary from case to case, but in general the lesion appears as a well circumscribed peripheral yellowish red mass with some associated exudation that usually extends from the lesion towards the posterior pole.”
As Dr. Elizalde pointed out, even cases with progressive exudation may develop a huge exudative retinal detachment. Patients with chronic pooling of exudate underneath the retina can finally develop subretinal fibrosis. Also some hemorrhage (intraretinal, subretinal or even within the vitreous cavity) may appear adjacent to the lesion. Cystoid macular edema, retinal pigment epithelium (RPE) proliferation and preretinal macular fibrosis can also be associated to these tumors.
---A and B ultrasound study demonstrated the 3.98 mm by 1.68 mm lesion and its high internal reflectivity pattern.
“Between 1995 and 2000 we treated 19 consecutive cases. They were all solitary and unilateral tumors. The lesion was located in the inferior, inferotemporal or temporal side of the fundus in 15 eyes (79%). In 6 cases (31.6%), the tumors were classified as idiopatic. In 13 cases (68.4%) they were associated with other preexisting ocular or periocular lesions, including retinitis pigmentosa (5 cases), Coats’ syndrome (4 cases), familial exudative vitreoretinopathy (1 case), post-traumatic chorioretinopathy (1 case), uveitis (1 case). One case had progressed after an active maxillary sinusitis surgery,” Dr. Elizalde said .
The most common vitreoretinal complications included intra- or subretinal exudation, vitreous hemorrhage, preretinal fibrosis, cystoid macular edema and posterior vitreous detachment.
The choice of treatment was based on the presence of potentially reversible causes of visual loss.
“Two tumors were asymptomatic and we decided to just keep them under observation,” Dr. Elizalde said. “They may remain stable for years or even regress spontaneously. Small lesions without extensive exudation (12 cases) were treated with laser photocoagulation or with external cryotherapy, which sometimes can induce dramatic tumor regression. Vitreoretinal surgery was necessary in 5 cases, in combination with laser or cryotherapy.”
He added that large and diffuse tumors (basal dimension greater than 10 mm) or cases that do not respond to other therapies can be managed by plaque radiotherapy. Also, in case of difficult diagnosis, transcleral resection of the lesion may be necessary.
“We had no such cases, but variables of this condition are many, and the best treatment option should be selected for every single case,” he said. “Combined techniques are often advisable.” Functional results are usually favorable. Visual acuity improved in 15 of our cases (84.2%), which is indeed a very good percentage.”
|Familial pigmentary dystrophy of the retina with some cysts near the optic disc in both eyes and lipid exudation in the left eye related to an inferiorly located peripheral vasoproliferative tumor.|
|External cryotherapy and laser photocoagulation of the tumor was performed and the exudation progressively disappeared.|
|Vasoproliferative tumor that progressed after an acute maxillary sinusitis surgery. An epiretinal proliferation within the macula was noted. Also intravitreal hemorrhages and some exudation extending from the inferior tumor towards the macula were observed.|
|Magnified photography of the macular area before (left) and after the vitreoretinal surgery (epiretinal membrane peeling and external cryotherapy of the tumor) with some cystoid macular edema still remaining (right).|
|Final result after 1, 3, 5 and 7 months after surgical treatment.|
For Your Information:
- Javier Elizalde, MD, can be reached at the Ocular Oncology Service, Centro de Oftalmología Barraquer, Muntaner 314, 08021 Barcelona, Spain; (34) 93-200-63-11; fax: (34) 93-200-24-69; e-mail: firstname.lastname@example.org. Dr. Elizalde has no direct financial interest in any of the products mentioned in this article, nor is he a paid consultant for any companies mentioned.
- Shields JA, Decker WL, et al. Presumed acquired retinal hemangiomas. Ophthalmol. 1983;90:1292-1300.
- Shields CL, Shields JA, et al. Vasoproliferative tumors of the ocular fundus: classification and clinical manifestation in 103 patients. Arch Ophthalmol. 1995;113:615-623.
- Irvine F, O’Donnell N, et al. Retinal vasoproliferative tumors: surgical management and histopathological findings. Arch Ophthalmol. 2000;118:563-569.