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the rarity of UM, timely completion of this large trial with embedded<br />

correlative studies appears feasible in the multicenter setting.<br />

Financial disclosure. None<br />

2212 UM18<br />

A CLINICAL PROBE FOR TRANSSCLERAL OPTICAL<br />

SPECTROSCOPY OF INTRAOCULAR TUMOURS<br />

J Krohn1,2, P Svenmarker3, CT Xu3, S Andersson-Engels3 (joerkroh@<br />

online.no)<br />

1. Department of Clinical Medicine, Section of Ophthalmology, University<br />

of Bergen, Bergen, Norway<br />

2. Department of Ophthalmology, Haukeland University Hospital,<br />

Bergen, Norway<br />

3. Department of Physics, Lund University, Lund, Sweden<br />

Purpose<br />

To develop a fiber optic probe for in vivo diagnosis of intraocular<br />

tumours by means of diffuse reflectance spectroscopy, and to optimize<br />

its geometric parameters for transmitting and receiving light through<br />

the sclera.<br />

Methods<br />

Two probe parameters were investigated: the source-detector distance<br />

and the fiber protrusion, i.e. length of the fibers extending from the probe<br />

end. Fluorescence stained choroidal tumour phantoms in enucleated<br />

porcine eyes were measured with diffuse reflectance- and laser-induced<br />

fluorescence spectroscopy. To evaluate the amount of light entering the<br />

tumour phantom, rather than merely the scleral tissue, the fluorescence<br />

from the phantoms was compared with the transmitted excitation light.<br />

The IOP and tissue temperature were monitored, and the scleral surface<br />

was imaged by scanning electron microscopy.<br />

Results. A fiber source-detector distance of 5 mm with 0 mm fiber<br />

protrusion provided maximum contrast of light interacting with the<br />

tumour phantom relative to light propagating between the fibers without<br />

entering into the phantom volume. Scleral applanation by the probe led<br />

to a mean IOP rise of 15 mm Hg. During spectroscopy, a temperature rise<br />

of 0.3 ºC was measured between the sclera and the tumour phantom.<br />

The indentation of the optical fibers did not cause any visible damage<br />

to the sclera.<br />

Conclusions. A source-detector distance of 5 mm with 0.5 mm fiber<br />

protrusion was considered optimal in terms of clinical and spectroscopic<br />

parameters. The study indicates that transscleral spectroscopy can be<br />

safely performed in human eyes, without leading to unacceptable IOP<br />

elevation, significant temperature rise, or scleral damage.<br />

Financial disclosure. Supported by grants from the Western Norway Regional Health Authority<br />

300 UM19<br />

OUR EXPERIENCE WITH TRANSPUPILLARY THERMO<br />

THERAPY FOR SUSPECTED OR SMALL CHOROIDAL<br />

MELANOMAS<br />

Mordechai Rosner, Iris Moroz , Josef Moisseiev, Victoria Vishnevskia-Dai<br />

(mrosner@post.tau.ac.il)<br />

Goldschleger Eye Institute, Sackler Faculty of Medicine, Tel-Aviv<br />

University, Sheba Medical Center, Tel-Hashomer, Israel<br />

Purpose. Changes in treatment approaches to choroidal melanomas<br />

resulted in better preservation of the eyeball and the visual acuity,<br />

UVEAL MELANOMA<br />

Abstracts<br />

102<br />

without increasing the mortality. As it is assumed that the initial spread<br />

of metastases is during the proliferating stage, it might be vital to<br />

diagnose and treat choroidal melanomas during the very early stages.<br />

In this presentation we summarize our experience with treatment of<br />

posterior choroidal nevi suspected for malignant transformation or small<br />

choroidal melanomas, less than 2.5 mm in thickness using Transpupillary<br />

Thermo Therapy (TTT).<br />

Methods. Six patients affected by small posterior choroidal melanoma<br />

were treated with TTT as a sole treatment from 2007 to 2011, and are<br />

followed up.<br />

Results. Six patients affected by small posterior choroidal melanoma<br />

were treated with TTT as a sole treatment from 2007 to 2011, and are<br />

followed up.<br />

Conclusions. TTT might be the treatment of choice for selected, very<br />

small melanomas. However, studies with long follow-up and large<br />

number of patients are needed to evaluate it effectiveness.<br />

Financial disclosure. None<br />

1842 UM20<br />

RESECTION OF IRIS TUMOURS : INTERNAL APPROACH<br />

Arun D. Singh M.D. (singha@ccf.org)<br />

Department of Ophthalmic Oncology, Cole Eye Institute, Cleveland Clinic<br />

Foundation, Cleveland, OH, USA<br />

Purpose. To describe a novel minimally invasive surgical technique for<br />

resection of small iris tumours.<br />

Methods. The surgical technique is described as “Small Incision Internal<br />

Resection and Aspiration.” Through a 3.0 mm beveled clear corneal<br />

incision a viscoelastic is instilled into the anterior chamber. Using 25 gauge<br />

horizontal vitrectomy scissors and vitrectomy forceps, the lesion is excised<br />

en bloc with a visible tumour free margin. A segment of clear plastic tubing<br />

(diameter 3.5 mm), primed with viscoelastic, is inserted into the anterior<br />

chamber through the enlarged corneal incision. Controlled aspiration<br />

allows removal of the entire lesion into the tube. The tube is then withdrawn<br />

from the anterior chamber and the lesion expressed onto filter paper. The<br />

iris defect is closed using a modified Siepser slip-knot technique. The larger<br />

corneal incision is closed with interrupted 10-0 nylon sutures.<br />

Results. This technique has been performed on 6 patients with localized<br />

iris tumours (base size : 5.0-1.7 mm) (hemangioma [1] and melanoma<br />

[5]). Reduced postoperative morbidity (inflammation, hypotony,<br />

astigmatism) allowed rapid uneventful recovery in all cases (Va 20/20).<br />

The histopathologic diagnosis could be established in each case and the<br />

margins were negative in all cases.<br />

Conclusions. Minimally invasive technique for resection of selected cases<br />

of iris tumours avoids the potential morbidity associated with a large<br />

corneoscleral incision allowing for rapid visual recovery.<br />

Financial disclosure. None<br />

1917 UM21<br />

PLAQUE RADIOTHERAPY TREATMENT WITH RUTHE-<br />

NIUM-106 FOR IRIS MALIGNANT MELANOMA<br />

Amit K. Arora, Maria Tsimpida, Victoria M.L. Cohen, John L. Hungerford<br />

(amitkarora@hotmail.com)<br />

St. Bartholomew’s Hospital and Moorfields Eye Hospital, London<br />

Purpose. To report results of Ruthenium-106 plaque radiotherapy for iris<br />

malignant melanoma

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