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12 Retina Gabriele K
299 12 Retina Gabriele K. Lang and Gerhard K. Lang 12.1 Basic Knowledge The retina is the innermost of three successive layers of the globe. It comprises two parts: ❖ A photoreceptive part (pars optica retinae), comprising the first nine of the 10 layers listed below. ❖ A nonreceptive part (pars caeca retinae) forming the epithelium of the cil- iary body and iris. The pars optica retinae merges with the pars ceca retinae at the ora serrata. Embryology: The retina develops from a diverticulum of the forebrain (proen- cephalon). Optic vesicles develop which then invaginate to form a double- walled bowl, the optic cup. The outer wall becomes the pigment epithelium, and the inner wall later differentiates into the nine layers of the retina. The retina remains linked to the forebrain throughout life through a structure known as the retinohypothalamic tract. Thickness of the retina (Fig. 12.1) Layers of the retina: Moving inward along the path of incident light, the individual layers of the retina are as follows (Fig. 12.2): 1. Inner limiting membrane (glial cell fibers separating the retina from the vitreous body). 2. Layer of optic nerve fibers (axons of the third neuron). 3. Layer of ganglion cells (cell nuclei of the multipolar ganglion cells of the third neuron; “data acquisition system”). 4. Inner plexiform layer (synapses between the axons of the second neuron and dendrites of the third neuron). 5. Inner nuclear layer (cell nuclei of the bipolar nerve cells of the second neuron, horizontal cells, and amacrine cells). 6. Outer plexiform layer (synapses between the axons of the first neuron and dendrites of the second neuron). -
(12) Patent Application Publication (10) Pub. No.: US 2013/0172829 A1 BADAW (43) Pub
US 2013 0172829A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2013/0172829 A1 BADAW (43) Pub. Date: Jul. 4, 2013 (54) DRY EYE TREATMENT SYSTEMS (52) U.S. Cl. CPC .................................... A61F 9/0008 (2013.01) (71) Applicant: SIGHT SCIENCES, INC., San USPC .......................................................... 604/294 Francisco, CA (US) (72) Inventor: Paul BADAWI, San Francisco, CA (US) (57) ABSTRACT (73) Assignee: SIGHT SCIENCES, INC., San Dry eye treatment apparatus and methods are described Francisco, CA (US) herein which generally comprise a patch or strip affixed to the skin of the upper and/or lower eyelids to deliver heat or other (21) Appl. No.: 13/645,985 forms of energy, pressure, drugs, moisture, etc. (alone or in combination) to the one or more meibomianglands contained (22) Filed: Oct. 5, 2012 within the underlying skin. The treatment strip or strips include one or more strips configured to adhere to an under Related U.S. Application Data lying region of skin in proximity to one or both eyes of a (63) Continuation-in-part of application No. 13/343,407, subject such that the one or more strips allow for the subject filed on Jan. 4, 2012. to blink naturally without restriction from the one or more patches. Moreover, the one or more Strips may be configured Publication Classification to emit energy to the underlying region of skin and where the one or more strips are shaped to follow a location of one or 51) Int.nt. CC. more me1bOm1amibomiam gland S COnta1nedined W1thinwithin the underlyingunderW1n A6DF 9/00 (2006.01) region of skin. -
MOC PORT/DOCK Practice Core Modules Content Outline
MOC PORT/DOCK Practice Core Modules Content Outline 1 Cataract and Anterior Segment (10%) 1.1 Basic Anatomical and Scientific Aspects 1.1.1 The Normal Lens 1.1.1.1 Anatomy 1.2 Assessment Techniques 1.2.1 History-Taking and Preoperative Examination of Ocular Structures 1.2.1.1 Take patient history 1.2.1.2 Examine ocular structures 1.2.1.3 Signs and symptoms 1.2.1.4 Indications for surgery 1.2.1.6 External examination 1.2.1.7 Slit-lamp examination 1.2.1.8 Fundus evaluation 1.2.1.9 Impact on visual functioning and quality of life 1.2.2 Measurement of Visual and Macular Function 1.2.2.1 Visual acuity testing 1.2.2.2 Test visual acuity 1.2.2.5 Visual field testing 1.2.2.6 Test visual field 1.2.2.7 Cataract's effect on visual acuity 1.2.2.8 Estimate cataract's effect on visual acuity 1.2.2.10 Measure visual (and macular) function 1.2.4.3 Evaluate glare disability: subjective and objective 1.3 Clinical Disease Conditions and Manifestations 1.3.1 Types of Cataract 1.3.1.1 Identify types of cataracts 1.3.2 Anterior Segment Disorders 1.3.2.1 Diagnose anterior segment disorders 1.3.2.2 Cataract associated with uveitis 1.3.2.3 Diabetes mellitus and cataract formation 1.3.2.4 Lens-induced glaucoma 1.3.2.4.1 Lens particle 1.3.2.4.2 Phacolytic 1.3.2.4.3 Phacomorphic Copyright and Use Policy for ABO Content Outlines © 2017 – American Board of Ophthalmology. -
Eyelids (2 Lec.)
Eyelids (2 lec.) Dr Abdulmelik shallal Anatomy: Eyelids are thin movable curtains composed of skin on their anterior surface and mucus membrane (conjunctiva) on the posterior surface, they contain: 1- Smooth muscles (Müller's muscles). 2- Striated muscles (Orbicularis oculi and Levator palpebrae superioris "LPS"). 3- Dense fibrous plates (Tarsal plates). 4- Glands. 5- Nerves and blood vessels. 1 The contents of the lid are distributed as follows: the anterior surface is made of skin which has a round edge with the lid margin, the subcutaneous tissue, muscular layer, the submuscular (areolar tissue) layer, the orbital septum which end as a tarsal plate (that forms the architecture of lid) and finally the conjunctiva (palpebral) which is situated most posterior. The free margin of the eyelids contains: 1- The lashes (Cilia). 2- Grey line. 3- Orifices of Meibomian glands. 4- Mucocutaneous junction 5- Superior and inferior puncti of Naso-Lacrimal System (NLS). Muscles of the eyelids: 1- Orbicularis oculi muscle: It is a thin oval sheet of concentric striated muscle surrounding the palpebral fissure. It can be divided into: a- Peripheral (orbital) part: This is involved in forceful closure of lids. b- Central (palpebral) part: This is involved in involuntary blinking, voluntary nonforceful closure and participates in forceful closure with the orbital part. c- Muscle of Rioland's: this part is represented by the gray line of lid margin. d- lacrimalis muscle: that attached to the fundus of lacrimal sac. This part is involved in pumping action of lacrimal drainage system. Nerve supply: Sensory: Ophthalmic branch of trigeminal nerve Motor: Facial nerve. -
Familial Hypercholesterolemia and Xanthomatosis Associated with Diabetes Mellitus: a Case Report and Review of the Literature Ch
Familial Hypercholesterolemia and Xanthomatosis Associated with Diabetes Mellitus: A Case Report and Review of the Literature Ching-Hsiang Leung, Tien-Ling Chen*, Chao-Hung Wang, Kun-Wu Tsan, and Daniel T. H. Chin** Division of Endocrinology and Metabolism, Department of Internal Medicine; *Division of Allergy, Immunology & Rheumatology, Department of Internal Medicine; **Department of Pathology; Mackay Memorial Hospital, Taipei, Taiwan Abstract Familial hypercholesterolemia is an autosomal dominant disorder due to mutations in the low-density lipoprotein receptor gene, characterized by skin and tendon xanthomas, xanthelasma and premature arcus corneae. It is associated with an increased risk of premature coronary heart disease, which is further increased if there is co-existing diabetes mellitus. A 35-year-old female who developed cutaneous and tendon xanthomas since the age of 12 was diagnosed as having mixed primary familial hypercholesterolemia and secondary hyperlipidemia due to diabetes mellitus, and osteomyelitis. However, familial hypercholesterolemia remains seriously under-diagnosed, delaying treatment. Screening of first-degree relatives and extended family members plays an important role in early detection and treatment. ( J Intern Med Taiwan 2003;14:23-30 ) Key Words:Familial hypercholesterolemia, Xanthomatosis, Diabetes mellitus, LDL receptor, Osteomyelitis Introduction Familial hypercholesterolemia is a monogenic 1 , autosomal dominant 2 disorder due to mutations in the gene for the LDL receptor 3, characterized by xanthomas 4, xanthelasma and premature arcus corneae 5. Our report concerns a 35-year-old female patient who developed xanthomas since the age of 12 and was diagnosed as having mixed primary familial hypercholesterolemia and secondary hyperlipidemia due to diabetes mellitus, and osteomyelitis. The significance, characteristic features, diagnosis and treatment of familial hypercholesterolemia are discussed. -
Erdheim-Chester Disease and Eyes
Erdheim-Chester Disease and Eyes OMAR OZGUR, MD OCTOBER 10, 2015 9:30- 10:00AM OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY AND ORBITAL ONCOLOGY FELLOW DEPARTMENT OF PLASTIC SURGERY THE UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER HOUSTON, TX, UNITED STATES Outline Anatomy and function of the eye and orbit Background and overview of ECD What can ECD do to the eye? DoubleDouble visionvision Pain Exophthalmos Overview of an eye exam General eye conditions that may also occur Droopy eyelids Dry eye syndrome Cataracts Refractive error Questions Please ask anytime! www.nasa.gov – Cat’s Eye Nebula Background anatomy https://c2.staticflickr.com/2/1363/542580866_940d2f9a02.jpg http://fiftylives.org/blog/wp- content/uploads/2012/08/Cornea.jpg Eye anatomy https://c2.staticflickr. com/2/1363/5425808 66_940d2f9a02.jpg http://www.retina-doctors.com/galleries/splash_patients/Eye%20anatomy%20-%20AN0003.jpg Optic nerves http://antranik.org/wp-content/uploads/2011/11/optic-nerve-lateral- geniculate-nucleus-of-thalamus-optic-radiation-visual-cortex.jpg?9873a6 http://www.vision-and-eye-health.com/images/GCA-AION.jpg Orbital anatomy http://www.leventefe.com.au/portfolio /mi-tec-medical-media-3/ http://msk- anatomy.blogspot.com/2014/12/ cranial-nerves-anatomy.html Eyelid structure http://eyestrain.sabhlokcity.com/2011/ 09/meibomian-gland-disease-mgd/ http://www.mastereyeassociates.com/blepharitis http://www.medindia.net/patients/patientinfo/gran ulated-eyelids.htm CT and MRI http://www.ijri.org/articles/2012/2 2/3/images/IndianJRadiolImaging_ -
Diagnosis and Management of Primary Biliary Cholangitis Ticle
REVIEW ArtICLE 1 see related editorial on page x Diagnosis and Management of Primary Biliary Cholangitis TICLE R Zobair M. Younossi, MD, MPH, FACG, AGAF, FAASLD1, David Bernstein, MD, FAASLD, FACG, AGAF, FACP2, Mitchell L. Shifman, MD3, Paul Kwo, MD4, W. Ray Kim, MD5, Kris V. Kowdley, MD6 and Ira M. Jacobson, MD7 Primary biliary cholangitis (PBC) is a chronic, cholestatic, autoimmune disease with a variable progressive course. PBC can cause debilitating symptoms including fatigue and pruritus and, if left untreated, is associated with a high risk of cirrhosis and related complications, liver failure, and death. Recent changes to the PBC landscape include a REVIEW A name change, updated guidelines for diagnosis and treatment as well as new treatment options that have recently become available. Practicing clinicians face many unanswered questions when managing PBC. To assist these healthcare providers in managing patients with PBC, the American College of Gastroenterology (ACG) Institute for Clinical Research & Education, in collaboration with the Chronic Liver Disease Foundation (CLDF), organized a panel of experts to evaluate and summarize the most current and relevant peer-reviewed literature regarding PBC. This, combined with the extensive experience and clinical expertise of this expert panel, led to the formation of this clinical guidance on the diagnosis and management of PBC. Am J Gastroenterol https://doi.org/10.1038/s41395-018-0390-3 INTRODUCTION addition, diagnosis and treatment guidelines are changing and a Primary biliary cholangitis (PBC) is a chronic, cholestatic, auto- number of guidelines have been updated [4, 5]. immune disease with a progressive course that may extend over Because of important changes in the PBC landscape, and a num- many decades. -
Management of Hyperlipidemias: an Update
Review MManagementanagement ofof hyperlipidemias:hyperlipidemias: AnAn updateupdate Article NNitinitin RRanjananjan Department of Dermatology, ABSTRACT Jawaharlal Nehru Medical College, Aligarh Muslim The discovery of the key enzymes, receptors, and transporters in cholesterol biosynthesis University, Aligarh, India has enabled us to assemble fragments of knowledge concerning lipids and lipoproteins into dynamic pathways, leading to the development of a multitude of lipid-lowering drugs. AAddressddress forfor ccorrespondence:orrespondence: Dr. Nitin Ranjan, Department After a brief recapitulation of the pathways of cholesterol metabolism and the dermatologic of Dermatology, Jawaharlal manifestations of lipid derangement, we shall review drugs which modify intestinal cholesterol Nehru Medical College, and bile-acid reabsorption, and hepatic lipoprotein biosynthesis and catabolism. The current Aligarh Muslim University literature is examined to determine future therapeutic targets in lipid metabolism, as well as (AMU), Aligarh - 202 001, the role of traditional foods as lipid-lowering agents. The latest National Cholesterol Education Uttar Pradesh, India. E-mail: [email protected] Program guidelines for managing hypercholesterolemia are also discussed. DOI: 10.4103/0378-6323.55387 Key words: Guidelines, Lipid metabolism, Low-density lipoprotein cholesterol, Statins PMID: ***** IINTRODUCTIONNTRODUCTION nascent CMs acquire cholesteryl esters (ChE), apo-C, and apo-E from HDL to form CMs. These CMs come Cholesterol serves not only as an essential component in contact with lipoprotein lipase (LPL) located on the of the cell membrane but also as the precursor luminal surface of vascular endothelium of skeletal molecule from which steroid hormones, bile salts, muscle and adipose tissue. LPL breaks down the and vitamin D are synthesized. It is both derived from triglyceride component of CMs into free fatty acids the diet and synthesized within the body, mainly in (FFA) and monoglycerides, in the process converting the liver. -
Ophthalmology
RAPID Ophthalmology mage i b e a in l n k n o Zahir Mirza Editorial Advisor: Andrew Coombes Rapid Ophthalmology To my supportive and ever thoughtful wife. Zahir Mirza Rapid Ophthalmology Dr Zahir Mirza, BSc, MBChB Ophthalmic Specialist Trainee Western Eye Hospital, Imperial NHS Trust London, UK Editorial Advisor Mr Andrew Coombes, BSc, MBBS FRCOphth Consultant Eye Surgeon Barts and the London NHS Trust London, UK A John Wiley & Sons, Ltd., Publication This edition first published 2013 C John Wiley & Sons, Ltd Wiley-Blackwell is an imprint of John Wiley & Sons, formed by the merger of Wiley’s global Scientific, Technical and Medical business with Blackwell Publishing. Registered office: John Wiley & Sons, Ltd, The Atrium, Southern Gate, Chichester, West Sussex, PO19 8SQ, UK Editorial offices: 9600 Garsington Road, Oxford, OX4 2DQ, UK The Atrium, Southern Gate, Chichester, West Sussex, PO19 8SQ, UK 111 River Street, Hoboken, NJ 07030-5774, USA For details of our global editorial offices, for customer services and for information about how to apply for permission to reuse the copyright material in this book please see our website at www.wiley.com/wiley-blackwell. The right of the author to be identified as the author of this work has been asserted in accordance with the UK Copyright, Designs and Patents Act 1988. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, except as permitted by the UK Copyright, Designs and Patents Act 1988, without the prior permission of the publisher. -
Mythbusters All Droopy Eyelids Are Created Equal
Financial disclosures Mythbusters Oculoplastic Edition Jed T. Poll, M.D. Utah Optometric Association June 3, 2016 Myth #1 Seriously…They’re all the same • Causes of “Droopy Eyelids” • Dermatochalasis All droopy • Blepharoptosis • Brow ptosis eyelids are • Pseudoptosis created equal I’m still not convinced… Different kinds-o-ptosis? Most common Usually congenital Dermatochalasis Ptosis Stretched tendon Weak muscle Excess skin problem Eyelid muscle problem High lid crease Absent lid crease Weighs down eyelid Lid margin / lashes low Involutional Myogenic Normal lid function Possible lid dysfunction Uncommon Uncommon Myasthenia / Botox Lesion / Mass Fluctuating Treat mass effect Many patients have both Neurogenic Mechanical 1 So…They’re not all the same Myth #1 • Correct Dx = Correct treatment – Not always surgical • Potential comorbidities All droopy – Droopy lid with… eyelids are • Anisocoria - Horner’s syndrome / CN III palsy • Fluctuations - Myasthenia Gravis created equal Myth #2 Will my insurance cover this? • Most common question for dermato and ptosis • 3 Elements: All eyelid – Complaint of visual impairment that improves with eyelid elevation surgery is – Supported by clinical exam – Documented with clinical photographs and cosmetic taped/untaped visual fields Dermatochalasis Evaluation Ptosis Evaluation • Exam: PF: lid margin to lid margin – “Grading” the amount of dermatochalasis MRD: light reflex to lid margin • 1+ to 4+ scale or mild to severe 1+ 2+ 3+ 4+ Dermatochalasis continuum Barely any Barely seeing 2 Ptosis Evaluation -
Biomarkers in Sebaceous Gland Carcinomas
3/24/2017 Biomarkers in Sebaceous Gland Carcinomas Sander R. Dubovy, MD Professor of Ophthalmology and Pathology Victor T. Curtin Chair in Ophthalmology Florida Lions Ocular Pathology Laboratory Bascom Palmer Eye Institute University of Miami Miller School of Medicine Biomarkers in Sebaceous Gland Carcinomas Disclosure of Relevant Disclosure of Relevant Financial Relationships Financial Relationships USCAP requires that all planners (Education Committee) in a position to Dr. Sander R. Dubovy declares he has no conflict(s) of interest influence or control the content of CME disclose any relevant financial to disclose. relationship WITH COMMERCIAL INTERESTS which they or their spouse/partner have, or have had, within the past 12 months, which relates to the content of this educational activity and creates a conflict of interest. Biomarkers in Sebaceous Gland Carcinomas Outline Introduction • Sebaceous carcinoma (SC) is a malignant neoplasm that arises from • Introduction to sebaceous cell carcinoma the sebaceous glands, most commonly in the periocular areas. • Incidence, demographics, risk factors • Clinical manifestations are often mistaken for benign conditions and • Ocular origins thus proper diagnosis and management is delayed. • Gross pathology • Metastases to regional lymph nodes and other sites are common. • Microscopic pathology • Immunohistochemistry • Management • Cases Biomarkers in Sebaceous Gland Carcinomas Biomarkers in Sebaceous Gland Carcinomas 1 3/24/2017 Introduction Sebaceous Gland • Pathologists should be aware of the -
Correlation of Corneal Arcus and Serum Lipid Profile
Original Research Article Correlation of corneal arcus and serum lipid profile Kiran Shetty1, Sarita Gonsalves2*, Shrinivas Gonagi3 1,2Assistant Professor, 3Professor, Dept. of, 1,2Father Muller Medical College, Mangaluru, Karnataka, 3DM WIMS Medical College, Wayanad, Kerala, India *Corresponding Author: Sarita Gonsalves Email: [email protected] Abstract Arcus senilis is depositionin the peripheral cornea and is considered a part of the normal ageing process usually seen in the elderly. However, there is a strong association of altered lipid metabolism and presence of arcus. We conducted a study at our hospital to find out if corneal arcus is an indicator of deranged lipid metabolism or only a consequence of normal ageing process. It was found that almost all patients with 360 degree corneal arcus had deranged lipid metabolism. Since eleveated serum lipids are a strong risk factor for cerebro vascular accidents and cardio vascular disease it is important to study the correlation between arcus and altered lipid profile. As slit lamp examination of arcus nis a simple, easy and inexpensive method to screen patients for hypercholesterolemia. Keywords: Arcus, Corneal arcus, Familial dysbetalipoproteinemia, Familial hypercholesterolemia. Introduction concluding the deposits to be due to lipids. Cornea has a Corneal arcus or arcus senilis is known to be a corneal temperature gradient which can affect the deposition of lipid finding in most of the aging population. It is has been s. It also has a gradient regarding how dense the collagen documented that at the age of 60 about 50-60% of the fibers of the cornea are packed and this effects what size of general human population have arcus and by the age of 80 particle can move towards the center.