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(cargusale@yahoo.com)<br />

Oncology Service, Wills Eye Institute, Philadelphia<br />

Purpose. To report the spectrum of iris lesions from a single ocular<br />

oncology center<br />

Methods. Retrospective review of medical records<br />

Results. Of 3451 patients, the mean age at presentation was 48 years<br />

(median 50 years, range 2 week to 95 years). There were 1423 males<br />

(41%) and 2028 females (59%). Of 3680 lesions, 2907 (79%) were<br />

benign and 773 (21%) were malignant, while 768 were cystic (21%)<br />

and 2912 (79%) solid. Specific diagnoses included nevus (41%), iris<br />

pigment epithelium (IPE) cyst (18%), melanoma (18%), freckle (3%),<br />

Lisch nodules (2%), melanocytoma (2%), melanocytosis (2%), and<br />

other (15%). Lesions were located in the iris stroma (80%) and IPE<br />

(20%). Most common diagnostic categories within solid lesions were<br />

melanocytic (68%), non-melanocytic (11%), vascular (2%), metastasis<br />

(2%) and pseudotumors (5%).<br />

Conclusions. Of 3680 iris lesions, 79% were benign; and the most<br />

common diagnosis included nevus (41%), IPE cyst (18%), melanoma<br />

(18%), and freckle (3%).<br />

Financial disclosure. None<br />

111 OT2<br />

CLINICAL AND OCT FINDINGS ON SYMPTOMATIC<br />

MACULAR NAEVI TREATED WITH INTRAVITREAL<br />

ANTI-VEGF<br />

Sonia A. Callejo, Mikael Sebag, Marc Blouin, Christine Corriveau<br />

(guilleyso@hotmail.com)<br />

Centre Hospitalier de l’Universite de Montreal CHUM Canada<br />

Purpose. To report the clinical and OCT findings of patients with<br />

symptomatic macular naevi treated with intraocular anti-VEGF.<br />

Methods. Retrospective small case series of 8 patients diagnosed<br />

with macular choroidal naevus with impared visual acuity treated<br />

with intravitreal anti-VEGF. Clinical information, serial color<br />

fundus photography, FA, OCT findings and ultrasonographic tumor<br />

measurements were reviewed and compared before and after anti-VEGF<br />

treatment.<br />

Results. 8 patients: 4 males and 4 females. Mean age at presentation:<br />

63 years (range 49 to 54). Mean follow up: 3 ½ years (range 7 months-9<br />

1/2 years). Mean number of anti-VEGF injections: 7.5 (range: 1 to 17).<br />

The largest naevus basal diameter was 7.3mm and the median thickness<br />

was 2.1mm. No ultrasonographic evidence of tumor enlargement or<br />

transformation into melanoma was documented following treatments.<br />

Large fluctuations in VA were recorded prior to anti-VEGF injections.<br />

Reduction in the degree of fluctuation was noticed during anti-VEGF<br />

treatments. Anti-VEGF treatment was associated with resolution or<br />

decreased of exudative retinal detachment, retinal thickness, cystic<br />

retinal changes (4 cases), subretinal fluid (6 cases), pigmented<br />

epithelium detachment (PED) (3 cases) and subretinal/intraretinal<br />

blood associated (1 case) or not (2 cases) to the presence of a choroidal<br />

endovascular membrane.<br />

Conclusions. Although a larger study is needed, the use of intraocular<br />

anti-VEGF treatment of symptomatic macular naevi is promising based<br />

on the improvement of clinical and OCT parameters as well as the<br />

stability of tumor measurements.<br />

Financial disclosure. None<br />

EYELID, CONJUNTIVA & ORBIT<br />

Abstracts<br />

71<br />

1340 OT3<br />

RISK FACTORS FOR GROWTH OF POSTERIOR UVEAL<br />

MELANOCYTIC LESIONS WITH THICKNESS GREATER<br />

THAN 2 MM IN 161 CONSECUTIVE PATIENTS<br />

Patrick De Potter, Audrey Noel, Jacques Jamart<br />

(patrick.depotter@uclouvain.be)<br />

Ocular Oncology Unit, Centre du Cancer, Cliniques Universitaires St Luc,<br />

Brussels, Belgium.<br />

Centre de Biostatistique et de Documentation médicale, Cliniques<br />

Universitaires de Mont-Godinne, Yvoir, Belgium<br />

Purpose. To better define the clinical and ultrasonographic risk factors<br />

predictive of growth of small melanocytic posterior uveal tumors<br />

presenting with a thickness of 2 mm or more as the only clinical suspicious<br />

factor predictive of tumor growth at first visit.<br />

Methods. Non comparative observational cases series including 161<br />

patients with suspicious choroidal or cilio-choroidal tumors measuring<br />

2 mm or more in thickness and no other clinical factors predicting of<br />

growth such as orange pigment, subretinal fluid, tumor margin touching<br />

disc, or tumor-related visual symptoms at initial visit. Those 161 patients<br />

were followed since October 1997 to document growth prior to treatment.<br />

Kaplan-Meier analysis was used to assess time to tumor growth and Cox<br />

proportional hazards regressions evaluated factors predictive of tumor<br />

growth<br />

Results. The mean age at diagnosis was 65 years old. The mean largest<br />

tumor diameter was 9 mm (range, 3 to 16 mm) and tumor thickness 2,6<br />

mm (range, 2 to 5,6 mm). The mean distance to the disc was 5,7 mm<br />

(range, 0,5 to 15 mm) and to the fovea 5,2 mm (range, 0 to 16 mm). Of<br />

the 161 small melanocytic lesions, 31 (19%) demonstrated growth after a<br />

mean follow-up of 32 months (range, 6 to 116 months). One patient (0.6%)<br />

developed systemic metastasis. The factors predictive of growth included<br />

greater tumor diameter, greater tumor thickness, lack of drusen, and<br />

acoustic hollowness. The global cumulative risks for tumor growth were<br />

4% at one year, 17% at 3 years, 22% at 5 years, and 27% at 10 years.<br />

Conclusions. Among posterior uveal melanocytic lesions with tumor<br />

thickness greater than 2.0 mm as the only clinical factor predictive of<br />

growth at initial visit, those with greater diameter, greater thickness,<br />

acoustic hollowness and lack of overlying drusen carried a significant risk<br />

for growth and should be monitored with regular surveillance.<br />

Financial disclosure. None<br />

6 OT4<br />

THE EXPANDING SPECTRUM OF RETINAL VASOPRO-<br />

LIFERATIVE TUMOURS<br />

Jerry A. Shields MD, David Reichstein MD, Arman Mashayekhi MD, Carol<br />

L. Shields MD (jerryshields@comcast.net)<br />

Wills Eye Institute<br />

Purpose. Retinal vasoproliferative tumor (RVPT) was originally<br />

described as an idiopathic fundus lesion with distinct clinical features.<br />

Subsequently, it found to be associated with a variety of ocular and<br />

systemic conditions and was subdivided into primary and secondary types.<br />

Methods. Review of lesions coded as retinal RVPT on the Oncology<br />

Service of Wills Eye Institute and literature search for causes of<br />

secondary retinal RVPTs<br />

Results. The secondary form of RVPT has now been associated with a

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