Bilateral Iridociliary T-Cell Lymphoma
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Glaucoma Related to Ocular and Orbital Tumors Sonal P
Chapter Glaucoma Related to Ocular and Orbital Tumors Sonal P. Yadav Abstract Secondary glaucoma due to ocular and orbital tumors can be a diagnostic challenge. It is an essential differential to consider in eyes with a known tumor as well as with unilateral, atypical, asymmetrical, or refractory glaucoma. Various intraocular neoplasms including iris and ciliary body tumors (melanoma, metasta- sis, lymphoma), choroidal tumors (melanoma, metastasis), vitreo-retinal tumors (retinoblastoma, medulloepithelioma, vitreoretinal lymphoma) and orbital tumors (extra-scleral extension of choroidal melanoma or retinoblastoma, primary orbital tumors) etc. can lead to raised intraocular pressure. The mechanisms for glaucoma include direct (tumor invasion or infiltration related outflow obstruction, tra- becular meshwork seeding) or indirect (angle closure from neovascularization or anterior displacement or compression of iris) or elevated episcleral venous pressure secondary to orbital tumors. These forms of glaucoma need unique diagnostic techniques and customized treatment considerations as they often pose therapeutic dilemmas. This chapter will review and discuss the mechanisms, clinical presenta- tions and management of glaucoma related to ocular and orbital tumors. Keywords: ocular tumors, secondary glaucoma, orbital tumors, angle infiltration, neovascular glaucoma, neoplastic glaucoma 1. Introduction With the advent of constantly evolving and advancing ophthalmic imaging tech- niques as well as surgical modalities in the field of ophthalmic diseases, diagnostic accuracy, and treatment outcomes of ocular as well as orbital tumors have improved remarkably over the past few years. Raised intraocular pressure (IOP) is known to be one of the presenting features or associated finding for numerous ocular as well as orbital tumors. Ocular and orbital tumors can cause secondary glaucoma due to various mechanisms. -
ICO Residency Curriculum 2Nd Edition and Updated Community Eye Health Section
ICO Residency Curriculum 2nd Edition and Updated Community Eye Health Section The International Council of Ophthalmology (ICO) Residency Curriculum offers an international consensus on what residents in ophthalmology should be taught. While the ICO curriculum provides a standardized content outline for ophthalmic training, it has been designed to be revised and modified, with the precise local detail for implementation left to the region’s educators. Download the Curriculum from the ICO website: icoph.org/curricula.html. www.icoph.org Copyright © International Council of Ophthalmology 2016. Adapt and translate this document for your noncommercial needs, but please include ICO credit. All rights reserved. First edition 201 6 . First edition 2006, second edition 2012, Community Eye Health Section updated 2016. International Council of Ophthalmology Residency Curriculum Introduction “Teaching the Teachers” The International Council of Ophthalmology (ICO) is committed to leading efforts to improve ophthalmic education to meet the growing need for eye care worldwide. To enhance educational programs and ensure best practices are available, the ICO focuses on "Teaching the Teachers," and offers curricula, conferences, courses, and resources to those involved in ophthalmic education. By providing ophthalmic educators with the tools to become better teachers, we will have better-trained ophthalmologists and professionals throughout the world, with the ultimate result being better patient care. Launched in 2012, the ICO’s Center for Ophthalmic Educators, educators.icoph.org, offers a broad array of educational tools, resources, and guidelines for teachers of residents, medical students, subspecialty fellows, practicing ophthalmologists, and allied eye care personnel. The Center enables resources to be sorted by intended audience and guides ophthalmology teachers in the construction of web-based courses, development and use of assessment tools, and applying evidence-based strategies for enhancing adult learning. -
Download Report Appendixes [PDF · 224
Appendices Appendix A. Selected Internet Links Appendix Table A1. Internet links for radiotherapy organizations Organization URL address Deutsche Gesellschaft fur http://www.degro.org/jsp_public/cms/index.jsp Radiooncologie European Society for Therapeutic http://www.estroweb.org/estro/index.cfm Radiology and Oncology American Society for Therapeutic http://www.astro.org/ Radiology and Oncology National Association for Proton http://www.proton-therapy.org/ Therapy Particle Therapy Cooperative http://ptcog.web.psi.ch/ Group (Accessed June 16, 2008) Appendix Table A2. Internet links for particle beam instrumentation companies Company URL address Ion Beam Applications (IBA) http://www.iba-worldwide.com/ Solutions Still River Systems Inc http://www.stillriversystems.com/ Optivus Proton Therapy http://www.optivus.com/ Siemens http://www.medical.siemens.com/ Hitachi: Proton beam Therapy http://www.pi.hitachi.co.jp/rd-eng/product/industrial-sys/accelerator- sys/proton-therapy-sys/proton-beam-therapy/index.html ACCEL Instruments http://www.proton-therapy.com/ (Accessed June 16, 2008) Appendix Table A3. Internet links for particle beam treatment centers in the USA Center/Institute URL address Francis H. Burr Proton Therapy http://www.massgeneral.org/cancer/about/providers/radiation/proton/i Center (NPTC) ndex.asp Loma Linda University Proton http://www.llu.edu/proton/index.html Therapy Center University of California, Crocker http://media.cnl.ucdavis.edu/crocker/website/default.php Nuclear Lab Midwest Proton Radiotherapy http://www.mpri.org/ Institute, Bloomington M.D. Anderson Proton Therapy http://www.mdanderson.org/care_centers/radiationonco/ptc/ Center, Houston University of Florida Proton http://www.floridaproton.org/ Therapy Institute, Jacksonville (Accessed June 16, 2008) A-1 Appendix B. -
Ocular Oncology and Pathology 2018 Hot Topics in Ocular Pathology and Oncology— an Update
Ocular Oncology and Pathology 2018 Hot Topics in Ocular Pathology and Oncology— An Update Program Directors Patricia Chévez-Barrios MD and Dan S Gombos MD In conjunction with the American Association of Ophthalmic Oncologists and Pathologists McCormick Place Chicago, Illinois Saturday, Oct. 27, 2018 Presented by: The American Academy of Ophthalmology 2018 Ocular Oncology and Pathology Subspecialty Day Advisory Committee Staff Planning Group Daniel S Durrie MD Melanie R Rafaty CMP DES, Director, Patricia Chévez-Barrios MD Associate Secretary Scientific Meetings Program Director Julia A Haller MD Ann L’Estrange, Subspecialty Day Manager Dan S Gombos MD Michael S Lee MD Carolyn Little, Presenter Coordinator Program Director Francis S Mah MD Debra Rosencrance CMP CAE, Vice R Michael Siatkowski MD President, Meetings & Exhibits Former Program Directors Kuldev Singh MD MPH Patricia Heinicke Jr, Copy Editor 2016 Carol L Shields MD Mark Ong, Designer Maria M Aaron MD Gina Comaduran, Cover Designer Patricia Chévez-Barrios MD Secretary for Annual Meeting 2014 Hans E Grossniklaus MD Arun D Singh MD ©2018 American Academy of Ophthalmology. All rights reserved. No portion may be reproduced without express written consent of the American Academy of Ophthalmology. ii Planning Group 2018 Subspecialty Day | Ocular Oncology & Pathology 2018 Ocular Oncology and Pathology Planning Group On behalf of the American Academy of Ophthalmology and the American Association of Ophthalmic Oncologists and Pathologists, it is our pleasure to welcome you to Chicago and -
Luth): a 15 Year Review
REVIEW OF MANAGEMENT OF ORBITO-OCULAR MALIGNANCIES IN LAGOS UNIVERSITY TEACHING HOSPITAL (LUTH): A 15 YEAR REVIEW BY DR. ADEWUMI OLABIMPE ALABI (MBBS, IBADAN) AF/012/11/002/554 A PART II DISSERTATION SUBMITTED IN PARTIAL FULFILMENT OF THE AWARD OF FELLOWSHIP IN RADIOTHERAPY, FACULTY OF RADIOLOGY, NATIONAL POSTGRADUATE MEDICAL COLLEGE OF NIGERIA. NOVEMBER, 2015 1 DECLARATION I declare that this study titled “REVIEW OF MANAGEMENT OF ORBITO- OCULAR MALIGNANCIES IN LAGOS UNIVERSITY TEACHING HOSPITAL (LUTH): A 15 YEAR REVIEW” was carried out by me and to the best of my knowledge contains no material previously published or written by another person, nor material which has been submitted or accepted for the award of any degree or Fellowship except where due acknowledgement has been made in the text. _______________________________ DR. ADEWUMI OLABIMPE ALABI (MBBS, IBADAN) 2 CERTIFICATION This is to certify that this research project “REVIEW OF MANAGEMENT OF ORBITO- OCULAR MALIGNANCIES IN LAGOS UNIVERSITY TEACHING HOSPITAL (LUTH) : A 15 YEAR REVIEW” was conducted in the Departments of Radiotherapy and Ophthalmology (Guinness Eye Centre), LUTH, Idi-araba, Lagos and Supervised by: Professor A. T. Ajekigbe Head, Department of Radiotherapy/Consultant Clinical & Radiation oncologist, Lagos University Teaching Hospital, Idi-araba, Lagos. Signature/Date: _____________________ Professor (Mrs) F. B. Akinsola Head, 3 Department of Ophthalmology/Consultant Ophthalmologist, Guinness Eye Centre, Lagos University Teaching Hospital, Idi-araba, Lagos. Signature/Date: _____________________ Department of Radiotherapy, Lagos University Teaching Hospital, Idi – araba, Lagos state. 2nd of August, 2015. This is to certify that this research project “REVIEW OF MANAGEMENT OF ORBITO- OCULAR MALIGNANCIES IN LAGOS UNIVERSITY TEACHING HOSPITAL (LUTH) : A 15 YEAR REVIEW” by Dr Alabi, Adewumi Olabimpe of the Department Of Radiotherapy, LUTH was conducted in the Departments of Radiotherapy and Ophthalmology (Guinness Eye Centre), LUTH, Idi-araba, Lagos State. -
Differential Diagnoses Symptoms and Other Useful Lists and Tables Signs for Ophthalmologists Case Presentations
Differential Diagnoses Symptoms and other Useful Lists and Tables Signs For Ophthalmologists Case Presentations Kenn Freedman MD PhD Department of Ophthalmology and Visual Sciences Texas Tech University Health Sciences Center Lubbock, Texas USA Acknowledgments and Disclaimer The differential diagnoses and lists contained herein are not meant to be exhaustive, but are to give in most cases the most common causes of many ocular / visual symptoms, signs and situations. Included also in these lists are also some less common, but serious conditions that must be “ruled-out”. These lists have been based on years of experience, and I am grateful for God’s help in developing them. I also owe gratitude to several sources* including Roy’s classic text on Ocular Differential Diagnosis. * Please see references at end of document This presentation, of course, will continue to be a work in progress and any concerns or suggestions as to errors or omissions or picture copyrights will be considered. Please feel free to contact me at [email protected] Kenn Freedman Lubbock, Texas - October 2018 Disclaimer: The diagnostic algorithm for the diagnosis and management of Ocular or Neurological Conditions contained in this presentation is not intended to replace the independent medical or professional judgment of the physician or other health care providers in the context of individual clinical circumstances to determine a patient’s care. Use of this Presentation The lists are divided into three main areas 1. Symptoms 2. Signs from the Eight Point Eye Exam 3. Common Situations and Case Presentations The index for all of the lists is given on the following 3 pages. -
Uveal Melanoma National Guidelines
Uveal Melanoma Guidelines – Draft for Consultation Uveal Melanoma National Guidelines Draft for public consulation June 2014 This project is the independent work of the Uveal Melanoma Guideline Development Group and is funded by Melanoma Focus (http://melanomafocus.com/) um_guideline_cons_draft_v2_23_6_14 Last saved by Nancy Turnbull Date 16 June 2014 Page 1 of 93 Uveal Melanoma Guidelines – Draft for Consultation Uveal Melanoma 1. Executive Summary ......................................................................................................................... 6 1.1 Care Pathway .......................................................................................................................... 6 1.2 Recommendations .................................................................................................................. 8 1.2.1 Patient Choice and Shared decision-making .................................................................. 8 1.2.2 Service Configuration ...................................................................................................... 8 1.2.3 General Guidance............................................................................................................ 8 1.2.4 Primary management ..................................................................................................... 9 1.2.5 Prognostication ............................................................................................................. 11 1.2.6 Surveillance .................................................................................................................. -
Uveal Melanoma National Guidelines
Uveal Melanoma Guidelines January 2015 Uveal Melanoma National Guidelines January 2015 Authors: Nathan P, Cohen V, Coupland S, Curtis K, Damato B, Evans J, Fenwick S, Kirkpatrick L, Li O, Marshall E, McGuirk K, Ottensmeier C, Pearce N, Salvi S, Stedman B, Szlosarek P, Turnbull N This project is the independent work of the Uveal Melanoma Guideline Development Group and is funded by Melanoma Focus (http://melanomafocus.com/) Page 1 of 112 Uveal Melanoma Guidelines January 2015 Uveal Melanoma 1. Executive Summary ......................................................................................................................... 6 1.1 Care Pathway .......................................................................................................................... 6 1.2 Recommendations ................................................................................................................ 10 1.2.1 Patient Choice and Shared decision-making ................................................................ 10 1.2.2 Service Configuration .................................................................................................... 10 1.2.3 General Guidance.......................................................................................................... 10 1.2.4 Primary management ................................................................................................... 11 1.2.5 Prognostication ............................................................................................................. 14 -
Ciliary Body Melanoma
Central JSM Ophthalmology Case Report *Corresponding author Maria Luisa Gois da Fonseca, Department of Retina and Vitreous, Federal Fluminense University Niterói, Marques do Parana Avenue 303 Centro- Niterói, Brazil, Ciliary Body Melanoma: A Case Tel: 24033900 21 26299000; Email: [email protected] Submitted: 20 April 2020 Report With A Satisfactory Accepted: 29 April 2020 Published: 30 April 2020 Clinical Evolution ISSN: 2333-6447 Copyright Carolina Correa Leal Lima, Maria Luisa Gois da Fonseca*, © 2020 Leal Lima CC, et al. Guilherme Herzog Neto and Raul Nunes Galvarro Vianna OPEN ACCESS Department of Retina and Vitreous, Federal Fluminense University Niterói, Brazil Keywords Abstract • Melanoma • Oculoplastics Ciliary body melanomas are rare uveal disorders. Due to its anatomical location, it • Oncology is usually incidentally discovered in advanced stages. There is no established treatment • Ophthalmology for metastatic disease and the one-year survival rate of these patients is only fifteen • Uveal melanoma percent. We intend to report a case of ciliary body melanoma with good clinical outcomes. INTRODUCTION Ciliary body melanomas represent twelve percent of the uveal melanomas. Usually asymptomatic, it is incidentally discovered in the sixth decade of life. Owing to the anatomy of the eye, commonly the diagnosis is only made in advanced stages [1]. The present article intends to report a ciliary body melanoma case and literature review. CASE PRESENTATION Male, 80 years, one-eyed, right eye vision loss after a central retinal vein occlusion that evolved to neovascular glaucoma, has been attended at Federal Fluminense University Hospital Antonio Pedro for left eye (LE), cataracts surgery evaluation. At the Figure 1 Biomicroscopy illustrating vascularized hyperpigmented examination, best-corrected visual acuity (BCVA), was no light nodular lesion between bulbar conjunctiva and inferior tarsus in the perception right eye (RE), and 20/50 LE. -
Primary Cysts of the Iris
PRIMARY CYSTS OF THE IRIS BY Jerry A. Shields, MD INTRODUCTION PRIMARY IRIS CYSTS ARE RELATIVELY UNCOMMON, AND THERE HAVE BEEN NO LARGE studies which define the clinical characteristics and natural course of these lesions. The purpose of this thesis is to summarize the available literature on primary iris cysts, to review the clinical data on 62 affected patients who have been evaluated and followed by the author, and to document their clinical features with anterior segment photographs. On the basis of these observations, certain misconceptions in the literature regarding primary iris cysts will be challenged and a simple classification of such lesions will be proposed. DEFINITIONS For purposes of this report a cyst is defined as an epithelial-lined space. A primary iris cyst is an epithelial-lined space which involves a portion of the iris and which has no recognizable etiology. A secondary iris cyst is an epithelial-lined space which involves a portion of the iris and which has a recognizable etiology, such as surgical trauma, nonsurgical trauma, or miotic drugs. Such secondary iris cysts have already been thoroughly and accurately described in the literature. They will be included in the overall classification but will not be included in the statistical part of this report. REVIEW OF THE LITERATURE The literature on primary iris cysts is rather confusing because most reports have cited only a single example or a small series of patients and no writer has accumulated enough cases to classify the lesions into clini- cally meaningful categories. A review of the available literature indicated that such cysts may occur on the pupillary margin, in the posterior epithelial layer of the iris, or as free-floating cysts in the aqueous or vitreous chambers. -
Pigmented Medulloepithelioma of the Ciliary Body
CLINICOPATHOLOGIC REPORTS, CASE REPORTS, AND SMALL CASE SERIES SECTION EDITOR: W. RICHARD GREEN, MD lomata acuminata. While receiving flamed fibrovascular cores Conjunctival Papillomas highly active antiretroviral therapy (Figure 2). Nucleated keratino- Caused by Human (HAART), including indinavir sul- cytes from the paraffin-embedded Papillomavirus Type 33 fate, nevirapine, and combivir, he has specimen were microdissected un- had no new opportunistic infections der direct visualization. After protein- Conjunctival papillomas are associ- and his CD4+ cell count has in- ase K digestion, DNA sequences for ated with human papillomavirus creased above 200/mm3. He sought HPV genotypes 16, 18, and 33 were (HPV) infection. In children, the le- ophthalmic care because of occa- amplified with a kit (PCR Human sions are typically manifestations of sional bleeding from the conjuncti- Papillomavirus Detection Kit; Pan an infection acquired during deliv- val lesions. An initial ocular exami- Vera, Madison, Wis) and transblot- ery.1 In adults, conjunctival papillo- nation revealed bilateral inferior ted for Southern blot hybridization. mas are most likely venereal and are palpebral conjunctival papillomas that Briefly, the common sense primer for often associated with anogenital le- were excised from the right eye. The HPV types 16, 18, and 33 was 5Ј- sions.2 Papillomas due to HPV more results of a histopathologic examina- AAGGGCGTAACCGAAATC- frequently progress to malignancy in tion showed conjunctival papillo- GGT-3Ј and the antisense primers of patients with the human immuno- mas without atypia. The results of an each HPV strain were as follows: 5Ј- deficiency virus (HIV) infection.3 Hu- immunohistochemistry test for HPV GTTTGCAGCTCTGTGCATA-3Ј for man papillomavirus types 6, 11, 16, types 6, 11, 16, 18, 31, and 33 was HPV 16, 5Ј-GTGTTCAGTTCCGT- and 18 have been identified in be- negative. -
Brachytherapy for Patients with Uveal Melanoma: Historical Perspectives and Future Treatment Directions
Journal name: Clinical Ophthalmology Article Designation: Review Year: 2018 Volume: 12 Clinical Ophthalmology Dovepress Running head verso: Brewington et al Running head recto: UM brachytherapy-early beginning to the molecular era open access to scientific and medical research DOI: 129645 Open Access Full Text Article REVIEW Brachytherapy for patients with uveal melanoma: historical perspectives and future treatment directions Beatrice Y Brewington1 Abstract: Surgical management with enucleation was the primary treatment for uveal melanoma Yusra F Shao2 (UM) for over 100 years. The Collaborative Ocular Melanoma Study confirmed in 2001 that Fredrick H Davidorf1 globe-preserving episcleral brachytherapy for UM was safe and effective, demonstrating Colleen M Cebulla1 no survival difference with enucleation. Today, brachytherapy is the most common form of radiotherapy for UM. We review the history of brachytherapy in the treatment of UM and the 1Havener Eye Institute, Department of Ophthalmology and Visual Science, evolution of the procedure to incorporate fine-needle-aspiration biopsy techniques with DNA- Ohio State University, 2Medical and RNA-based genetic prognostic testing. Student Research Program, The Ohio Keywords: brachytherapy, uveal melanoma, UM, fine-needle-aspiration biopsy, genetic State University College of Medicine, Columbus, OH, USA prognostic testing, molecular markers Introduction In the early 1900s, patients often presented with large, symptomatic uveal melanoma (UM), for which the primary course of treatment was enucleation.