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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