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The Retinoblastoma Center of Houston; MD Anderson Cancer Center; Texas Children’s Cancer Center; The Methodist Hospital Research Institute; Baylor College of Medicine, Houston, Texas, USA Purpose. Massive ischemia and necrosis can occur in advanced cases of retinoblastoma. Few reports have documented clinical findings just prior to and just after the ischemic event. Methods. A single case report. Results. The case will demonstrate the clinical findings just prior to and after a massive ischemic event in a patient with bilateral retinoblastoma. Photographic, radiographic and histologic correlation will be presented. Conclusions. This case demonstrates the atypical findings that can occur in advanced eyes with retinoblastoma that develop a massive ischemic event. Financial disclosure. Dr. Gombos is a member of the Children’s Oncology Group and has received reimbursement for travel. He is a paid consultant for IMS Health. 121 RF7 SUPRA-SELECTIVE CATHETERIZATION OF THE OPH- THALMIC ARTERY FOR INTRA-ARTERIAL CHEMO- THERAPY INJECTION IN RETINOBLASTOMA Vicktoria (Vicky)Vishnevskia-Dai1, Iris Moroz1 , Joseph Moisseiev, Mordechai Rosner1, Mati Bakon2 (vivida65@gmail.com) 1.Goldschleger Eye Institute, Sheba Medical center, Sackler School of medicine, Tel-Aviv University Israel. 2. Invasive neuro-radiology center, Sheba Medical center, Sackler School of medicine, Tel-Aviv University Israel. Purpose. A 3-year old girl with unilateral group D retinoblastoma was treated with Supra-selective catheterization of the ophthalmic artery and intraarterial melphalan injections. Financial disclosure. None 1957 RF8 PARANEOPLASTIC VITELLIFORM RETINOPATHY M. Turell1, G. Adamus2, Y. Wang3, C.C. Chan3, A. Singh1 (turellm2@ccf.org) 1. Department of Ophthalmic Oncology, Cole Eye Institute, Cleveland Clinic, Cleveland, OH 2. Casey Eye Institute, Oregon Health & Science University, Portland, OR 3. Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, MD Purpose. An 80-year old man was referred for evaluation of choroidal metastases. The case will be presented as an unknown for opinions from the audience. Methods. Fundus photos, Fluorescein angiography, and OCT are presented. Results. Ophthalmic imaging exludes the possibility of choroidal metastases. Serum autoantibodies additionally confirm the paraneoplastic nature of the disease. Conclusions. The clinical picture is consistent with the rare disease, paraneoplastic vitelliform retinopathy. Financial disclosure. None Rapid Fire Cases Abstracts 76 214 RF9 CILIARY BODY TUMOR IN A CHILD Adriana C. Fandiño MD, Raslawsky E. Cristina MD, Chantada Guillermo MD (acfandino@gmail.com) Ophthalmology Department; Radiotherapy Department; Hematooncology Department, Hospital de Pediatria J.P.Garrahan, Buenos Aires, Argentina Purpose. When a 10-year-old boy presented with rapid visual loss because of progressive astigmatism, a ciliary body mass with rapid progression was found. Methods. It was assumed to be a medulloepithelioma and treated with brachytherapy. Results. The patient had an excellent course with more than eight year follow-up. Conclusions. The case will be presented for opinions from the audience Financial disclosure. None 418 RF10 RETINAL DETACHMENT AFTER FNAB Arturo Irarrazaval, Pablo Cazón (artuira@consultoresoftalmologicos.com) Consultores Oftalmológicos Purpose. To show a case where after the FNAB a retinal detachment that did not resolve occurred. Methods. Retrospective study of the patient chart Results. The patient was first treated with pneumatic retinopexy, and after that with vitrectomy, which resolved the detachment. Conclusions. FNAB, although rarely, can produce a retinal detachment, that can be succesfully treated with retina surgery. Financial disclosure. None 2047 RF11 DIFFUSE MELANOCYTIC NEOPLASM IN A 9 YEAR-OLD FEMALE WITH OCULODERMAL MELANOCYTOSIS A.C. Schefler, A.M. Schimel, A. Abbey, E. Hodapp, S.R. Dubovy (aschefler@med.miami.edu) Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida, U.S.A. Purpose. This is an unusual case of a diffuse melanocytic malignancy involving 360 degrees of the ciliary body and the entire choroid in a 9 year-old girl with oculodermal melanocytosis. The patient presented with melanocytomalytic glaucoma and ultimately underwent enucleation. Extensive clinical photographs and histopathology will be shown. Financial disclosure. None 2251 RF12 A CASE OF ADENOMA OF THE NON-PIGMENTED CILIARY EPITHELIUM CAUSING NEOVASCULAR GLAUCOMA Vasilios P. Papastefanou, Victoria ML Cohen (bazmed@hotmail.com)
Ocular Oncology Service, St Bartholomew`s Hospital and Moorfields Eye Hospital, London, UK Purpose. A 67-year old Caucasian man presented with rapidly reducing vision in the right eye. Reduced vision was attributed to cataract and he underwent routine cataract surgery. However, intraoperatively a solid mass was noted. The patient was referred to the Ocular Oncology Service. Methods. Transillumination did not reveal a clear shadow and B scan ultrasound revealed a ciliary body mass with internal blood flow and medium internal reflectivity. An incisional biopsy was performed. The histology results are discussed. A diagnosis of ciliary body adenoma of the non-pigmented epithelium (NPCE adenoma) was made. Results. One year later, patient developed hyperemia with blurred vision in the affected eye. He had marked episcleral injection, an oedematous cornea, marked rubeosis and angle closure. The intraocular pressure was 42 mmHg. The ciliary body adenoma remained unchanged . The tumour was treated with plaque radiotherapy (Ru-106) in order to restrict the neovascular response. Treatment was successful in reducing the tumour size on B-scan ultrasonography. Intracameral injections of bevacizumab where required pre- and postoperatively to control the rubeosis. Conclusions. To our knowledge, this is the first report of neovascular glaucoma secondary to a ciliary body adenoma. Financial disclosure. None 1934 RF13 CHOROIDAL NEVUS...CHOROIDAL NEVUS? Miguel A. Materin, Ruth Halaban, Antonella Bacchiocchi (miguel.materin@yale.edu) Yale School of Medicine Purpose. 10 years follow up on a typical choroidal nevus Conclusions. To be discussed at the meeting. Financial disclosure. None 2312 RF14 MUSHROOM SHAPED TUMOR. MELANOMA OR NOT? Jerry Shields, MD (jerryshields@comcast.net) Wills Eye Institute Purpose. To present a mushroom shaped tumor Methods. Review of case Results. Diagnosis and management Conclusions. A mushroom shaped tumor could be melanoma or something else. Financial disclosure. None 104 RF15 AMELANOTIC INTRAOCULAR LESION IN A 26 YEAR- OLD FEMALE PATIENT Luiz F. Teixeira1,2, Carla R. D. Macedo2, Carlos A.G. Filho1, Camila H. Hashimoto2, Marcia Lowen3, Maria C. Martins1 (luizfteixeira@hotmail.com) 1. Department of Ophthalmology- Federal University of Sao Paulo- UNIFESP 2. Pediatric Oncology Institute/GRAACC/UNIFESP 3. Department of Pathology- Federal University of Sao Paulo Rapid Fire Cases Abstracts 77 Purpose. A 26 year-old female patient presented with an unusual intraocular lesion. It will be presented as a mysterious case for discussion. Financial disclosure. None 2328 RF16 PIGMENTED ANTERIOR SEGMENT TUMOR IN A YOUNG MAN Carolina M. Gentile, Camila Challiol, Atilio Lombardi, J. Oscar Croxatto (carolina.gentile@gmail.com) Hospital Italiano de Buenos Aires, Argentina Purpose. The aim of the presentation is to discuss the diagnosis and management of an anterior melanocytic segment tumor in a young adult. Methods. A 38 years-old male high mountain climber presented with a growing anterior segment pigmented mass. Diagnosis and management will be discussed with the audience. It will be presented as an unknown case for opinions. Results. Fine needle aspiration biopsy was performed and the diagnosis was melanocytoma. Conclusions. Anterior uveal melanocytomas are uncommon benign melanocytic tumors. Despite the benign nature of iris melanocytoma, growth was observed and histologic confirmation was necessary to establish a diagnosis and ruled out malignancy. Financial disclosure. None 2254 RF17 AMELANOTIC CHOROIDAL MASS EXTENDING TO THE FOVEA Zelia M. Correa, MD, PhD, James J. Augsburger, MD (correazm@uc.edu) Dept of Ophthalmology, University of Cincinnati, Cincinnati, OH, USA Purpose. Case presentation Methods. A 66-year-old asymptomatic Caucasian female was found to have a choroidal mass measuring 14 X 12 mm in base and 2.5 mm in thickness, extending to the fovea +/- SRF on routine eye exam. Results. The importance of accurate diagnosis will be discussed. Conclusions. Clinical diagnosis impacts management decision. Financial disclosure. None 29 RF18 PIGMENTED CHOROIDAL TUMOR Jacob Pe’er, MD, Shahar Frenkel, MD, PhD (peer@hadassah.org.il) Specialized Ocular Oncology Service, Department of Ophthalmology, Hadassah - Hebrew University Medical Center, Jerusalem, Israel Purpose. An 84-year-old woman presented with elevated (6.9 mm) pigmented lesion with retinal and choroidal hemorrhage around it. The lesion was diagnosed as choroidal melanoma and treated using brachytherapy, with good response. One year later regrowth was noticed, and the eye was enucleated. There was a surprise in the histopathologic examination. Financial disclosure. None
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XV th NH City Hotel and Tower Boliv
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List of Congress Meetings of the In
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Table of Contents Welcome address K
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Keynote Lectures Lymphoma of the oc
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The venue for the Biannual Meeting
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Buenos Aires Downtown MAP 12 Venue
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MORNING 8.30-10.10 Papers (Moderato
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50 RES 26 USING THE GLYCOLYTIC INHI
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2226 RES 4 NOTCH SIGNALING PROMOTES
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a reduction in the number of living
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array further detected copy number
Page 25 and 26: 615 RES 21 TRB2 AND SKP2 IN THE RET
Page 27: following treatment with 2-fluorode
Page 30 and 31: 1909 Rb14 RESULTS OF PATIENTS WITH
Page 32 and 33: Posters Retinoblastoma 2006 RBp100
Page 34 and 35: 120 RBp135 MANAGEMENT OF AN ECTOPIC
Page 36 and 37: After treatment, 10 patients lived
Page 38 and 39: Methods. Six cycles of carboplatin
Page 40 and 41: 1940 RB15 PROTON THERAPY FOR RECURR
Page 42 and 43: 4. Fluoroscopy for cannula placemen
Page 44 and 45: Methods. A retrospective chart revi
Page 46 and 47: Ruth A. Kleinerman1, Chu-ling Yu1,
Page 48 and 49: 2006 RBp100 RETINOBLASTOMA ASSESSME
Page 50 and 51: months. Mean delay between beginnin
Page 52 and 53: not associated with severity of RB.
Page 54 and 55: Conclusions. During a ten-year peri
Page 56 and 57: 30 RBp127 TREATMENT MODULATION IN R
Page 58 and 59: (follow-up 5 years). Two years afte
Page 61 and 62: 8.30-9.00 Poster presentations ECOp
Page 63 and 64: Uvea (Moderators: B. Damato, M. Sag
Page 65 and 66: Morning 8.30-9.00 Poster presentati
Page 67 and 68: 1621 EC1 EVALUATION OF THE “HEDGE
Page 69 and 70: Purpose. Ocular surface squamous ne
Page 71 and 72: (cargusale@yahoo.com) Oncology Serv
Page 73 and 74: of the tissues most commonly affect
Page 75: 2128 RF1 RETINOBLASTOMA David H. Ab
Page 79 and 80: Arturo Irarrazaval, Pablo Cazon, Os
Page 81 and 82: A CASE OF TEARING AND SWELLING OF T
Page 83 and 84: 1849 ECp101 FIVE CASES OF CARCINOMA
Page 85 and 86: patients. The isolated involvement
Page 87 and 88: exudative fluid from the hemangioma
Page 89: maximum of 7 rituximab injections.
Page 92 and 93: 153 UM14 PHENO-GENOTYPIC IDENTIFICA
Page 94 and 95: 8.30-9.00 Poster presentations UMp1
Page 96 and 97: 2253 UM1 PRELIMINARY STUDY OF VASCU
Page 98 and 99: Purpose. To determine the presence
Page 100 and 101: gene expression profile of melanocy
Page 102 and 103: the rarity of UM, timely completion
Page 104 and 105: C. Metz, T. Gkika, W. Sauerwein, N.
Page 106 and 107: Patients in the triamcinolone group
Page 108 and 109: 1350 Ump101 INDUCED EXPRESSION OF P
Page 110 and 111: Purpose. To report the Results of R
Page 112 and 113: 1547 Ump113 LONG-TERM OBSERVATIONS
Page 114 and 115: 2038 Ump119 VALUE OF DOPPLER ANALYS
Page 116: Methods. A total of 4070 patients w
Page 119: First authors Naseripour, Masood No
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