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exudative fluid from the hemangioma. Collapse of this structure may be<br />

the origin of an epiretinal membrane.<br />

Conclusions. Intraoperative PDT therapy is an option in pediatric VHL<br />

patients with peripapillary hemangiomas. Technique for this procedure<br />

performed under general anesthesia will be discussed.<br />

Financial disclosure. None<br />

105 OTp103<br />

MEK INHIBITOR-ASSOCIATED SEROUS RETINOPATHY<br />

- CLINICAL FEATURES OF A NEW RETINAL DISORDER<br />

Scott C. N. Oliver, Raul Velez Montoya, Wells Messersmith, Jeffrey L<br />

Olson, Naresh Mandava (scott.oliver@ucdenver.edu)<br />

Departments of Ophthalmology and Medical Oncology, University of<br />

Colorado School of Medicine, USA<br />

Purpose. MAPK/ERK kinase (MEK) inhibitors are a promising class<br />

of antineoplastic agents undergoing human clinical trial. This report<br />

describes new findings of serous retinopathy and outer retinal thickening<br />

not previously reported with these agents<br />

Methods. Retrospective review<br />

Results. Three patients with metastatic cancer had multiple central<br />

scotomas 1,3, and 14 days after study drug initiation. Subneurosensory<br />

fluid (SRF) was visible clinically and on optical coherence<br />

tomography(OCT). Additionally, OCT identified diffuse outer retinal<br />

thickening in areas not associated with fluid. FA and ICG angiography<br />

did not show leakage. Findings resolved with drug discontinuation.<br />

Conclusions. MEK inhibitor associated serous retinoapathy consists<br />

of rapid onset localized SRF and diffuse outer retinal thickening. It<br />

resembles, but is distinct from CSR, and requires further investigation.<br />

Financial disclosure. Dr. Oliver is a consultant with Array Bioscience, Inc.<br />

1450 OTp104<br />

BENIGN TUMORS OF CILIARY BODY IN KOREAN<br />

PATIENTS<br />

Christopher Seungkyu Lee1A, Hee Jung Kwon1A, Hyae Min Jeon1B, Min<br />

Kim1A, Sung Chul Lee1A (sklee219@yuhs.ac)<br />

(A) Department of Ophthalmology,<br />

(B) Department of Pathology,<br />

(1) Yonsei University College of Medicine, Seoul, Korea<br />

Purpose. To evaluate clinical features, management, histopathology,<br />

and prognosis of benign ciliary body tumors in Korean patients.<br />

Methods. A retrospective medical chart review was conducted on various<br />

benign tumors of ciliary body that were evaluated by the authors between<br />

2006 and 2011.<br />

Results. All 8 patients underwent transscleral local resection of ciliary<br />

body tumors, which were pathologically confirmed to be benign. Of 8, 3<br />

were diagnosed with adenoma of nonpigmented ciliary body epithelium<br />

(2 men, 1 woman; mean age 35 years; mean initial and final visual acuities<br />

(VAs) 20/25 and 20/32 over 2 years), 1 was adenoma of pigmented ciliary<br />

body epithelium (woman; 83 years; mean initial and final VAs 20/200<br />

and light perception over 1 month), 2 were melanocytoma (2 men; mean<br />

age 40 years; mean initial and final VAs 20/25 and 20/25 over 2 years),<br />

1 was schwannoma (woman; 30 years; initial and final VAs 20/100 and<br />

detecting hand movement over 5 years), and 1 was leiomyoma (woman;<br />

46 years; initial and final VAs 20/400 and 20/80 over 1.5 years).<br />

EYELID, CONJUNTIVA & ORBIT<br />

Abstract Posters<br />

87<br />

Conclusions. Various benign tumors can be found in the ciliary body<br />

that should be differentiated from malignant tumors, especially ciliary<br />

body melanoma. Benign ciliary body tumors are rare and each type of<br />

tumor has its characteristic clinical and histopathological features that<br />

can suggest the diagnosis. In the management of these tumors, local<br />

resection, rather than enucleation, should be considered first as the<br />

treatment of choice. The visual prognosis was fair without any systemic<br />

morbidity.<br />

Financial disclosure. None<br />

321 OTp105<br />

TREATMENT OF SEROUS MACULAR DETACHMENT<br />

ASSOCIATED WITH CIRCUMSCRIBED CHOROIDAL<br />

HEMANGIOMA<br />

Sung Chul Lee, Hee Jung Kwon, Min Kim, Christopher Seungkyu Lee<br />

(sunglee@yuhs.ac)<br />

Department of Ophthalmology, Institute of Vision Research, Yonsei<br />

University College of Medicine, Seoul, Korea<br />

Purpose. To evaluate the effect of transpupillary thermotherapy<br />

(TTT) and intravitreal injection of bevacizumab (IVB) on serous<br />

macular detachment (SMD) associated with circumscribed choroidal<br />

hemangioma (CCH).<br />

Methods. We retrospectively reviewed the records of CCH patients<br />

treated by TTT and/or IVB to reduce SMD. We assessed changes in<br />

visual acuity (VA), resolution of SMD and central fovea thickness (CFT) by<br />

optical coherence tomography (OCT).<br />

Results. Of 8 patients treated with TTT, 5 patients showed complete<br />

resolution of SMD in OCT with improvement of median LogMAR VA from<br />

0.7 to 0.22 (p=0.042). These 5 patients showed no recurrence of SMD<br />

for a mean duration of 51.8 months, but SMD finally recurred in 4 of<br />

them.<br />

Of 9 patients treated with IVB, 5 patients showed resolution of SMD with<br />

a decrease of median CFT from 514 µm to 330 µm (p=0.043). Of these 5<br />

patients, 2 patients showed recurrence of SMD after 6.2 months.<br />

In TTT group, 5 patients (3 patients in complete SMD resolution group,<br />

2 patients in persistent SMD group) received additional IVB and 4 of<br />

them also had cystoids macular edema (CME) with SMD before IVB.<br />

All the patients showed persistent CME after IVB despite the complete<br />

resolution of SMD in two of them.<br />

Conclusions. In some patients with SMD in CCH, both TTT and IVB may<br />

be used effectively. However, the duration of treatment effectiveness<br />

appears to be longer in TTT than that in IVB. IVB for recurred SMD after<br />

TTT Results in variable outcome but IVB had no effect on CME.<br />

Financial disclosure. None<br />

2132 OTp106<br />

INTRAOCULAR RELAPSE OF MULTIPLE MYELOMA<br />

RESPONSIVE TO BORTEZOMIB<br />

Tero Kivelä (tero.kivela@helsinki.fi)<br />

Department of Ophthalmology, Helsinki University Central Hospital,<br />

Helsinki, Finland<br />

Purpose. To report complete response to systemic bortezomib of a<br />

relapse of multiple myeloma in the iris.<br />

Methods. A 60-year-old man was diagnosed with multiple myeloma,

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