Affections of Uvea Affections of Uvea
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Passport to Success
The following terms and other boldface terms in the chapter are defined in the Glossary accommodation choroid After careful study of this chapter, you should be able to: cochlea conjunctiva 1. Describe the function of the sensory system convergence 2. Differentiate between the special and general senses and give examples of each cornea 3. Describe the structure of the eye gustation 4. List and describe the structures that protect the eye lacrimal apparatus 5. Define refraction and list the refractive parts of the eye lens (crystalline lens) 6. Differentiate between the rods and the cones of the eye olfaction 7. Compare the functions of the extrinsic and intrinsic muscles of organ of Corti the eye ossicle 8. Describe the nerve supply to the eye proprioceptor 9. Describe the three divisions of the ear refraction 10. Describe the receptor for hearing and explain how it functions retina 11. Compare static and dynamic equilibrium and describe the sclera location and function of these receptors semicircular canal 12. Explain the function of proprioceptors sensory adaptation 13. List several methods for treatment of pain sensory receptor 14. Describe sensory adaptation and explain its value tympanic membrane 15. Show how word parts are used to build words related to the vestibule sensory system (see Word Anatomy at the end of the chapter) vitreous body PASSport to Success Visit thePoint or see the Student Resource CD in the back of this book for definitions and pronun- ciations of key terms as well as a pretest for this chapter. ® Paul’s Second Case: Seeing More of the Sun’s Effects aul glanced once again at the postcard condition, and it does have a hereditary fac- sitting on his entranceway table as he ar- tor.” The doctor dilated Paul’s eyes with drops Prived home in the evening. -
The Behavior of Fibroblasts from the Developing Avian Cornea
THE BEHAVIOR OF FIBROBLASTS FROM THE DEVELOPING AVIAN CORNEA Morphology and Movement In Situ and In Vitro JONATHAN B. L. BARD and ELIZABETH D. HAY From the Department of Anatomy, Harvard Medical School, Boston, Massachusetts 02115. Dr. Bard's present address is the Medical Research Council Unit, Western General Hospital, Edinburgh 4, Scotland. ABSTRACT The early chick cornea is composed of an acellular collagenous stroma lined with an anterior epithelium and a posterior endothelium. At stage 2?-28 of development (51/2 days), this stroma swells so that the cornea is 75 120 #m thick. At the same time, fibroblasts that originate from the neural crest begin to invade this stroma. Using Nomarski light microscopy, we have compared the behavior of moving cells in isolated corneas with the migratory activities of the same cells in artificial collagen lattices and on glass. In situ, fibroblasts have cyclindrical bodies from which extend several thick pseudopodia and/or finer filopodia. Movement is accompanied by activity in these cytoplasmic processes. The flat ruffling lamelli- podia that characterize these cells on glass are not seen in situ, but the general mechanism of cell movement seems to be the same as that observed in vitro: either gross contraction or recoil of the cell body (now pear shaped) into the forward cell process, or more subtle "flowing" of cytoplasm into the forward cell process without immediate loss of the trailing cell process. We filmed collisions between cells in situ and in three-dimensional collagen lattices. These fibroblasts show, in their pair-wise collisions, the classical contact inhibition of movement (CIM) ex- hibited in vitro even though they lack ruffled borders. -
Clinical Study of Etiopathogenesis of Isolated Oculomotor Nerve Palsy
CLINICAL STUDY OF ETIOPATHOGENESIS OF ISOLATED OCULOMOTOR NERVE PALSY DISSERTATION SUBMITTED TO In partial fulfillment of the requirement for the degree of M.S. DEGREE EXAMINATION OF BRANCH III OPHTHALMOLOGY of THE TAMIL NADU DR. M. G. R MEDICAL UNIVERSITY CHENNAI- 600032 DEPARTMENT OF OPHTHALMOLOGY TIRUNELVELI MEDICAL COLLEGE TIRUNELVELI- 11 APRIL 2015 CERTIFICATE This is to certify that this dissertation entitled “Clinical Study Of Etiopathogenesis Of Isolated Oculomotor Nerve Palsy” submitted by Dr. Saranya.K.V to the faculty of Ophthalmology ,The Tamil Nadu Dr. MGR Medical University, Chennai in partial fulfillment of the requirement for the award of M.S Degree Branch III (Ophthalmology), is a bonafide research work carried out by her under my direct supervision and guidance. Dr. L.D.THULASI RAM MS. (Ortho) Dr A.YOGESWARI. The Dean Professor & Head of the Department Tirunelveli Medical College, Department of Ophthalmology Tirunelveli Tirunelveli Medical College, Tirunelveli. DECLARATION BY THE CANDIDATE I hereby declare that this dissertation entitled “Clinical Study Of Etiopathogenesis Of Isolated Oculomotor Nerve Palsy” is a bonafide and genuine research work carried out by me under the guidance of Dr. RITA HEPSI RANI .M, Assistant Professor of Ophthalmology, Department of Ophthalmology, Tirunelveli Medical College, Tirunelveli Dr. Saranya.K.V Post Graduate In Ophthalmology, Department Of Ophthalmology, Tirunelveli Medical College, Tirunelveli. ACKNOWLEDGEMENT I express my sincere gratitude and thanks to The Dean, Tirunelveli Medical College, Tirunelveli, for providing all the facilities to conduct this study. I sincerely thank Dr.A.Yogeswari Professor and HOD, Dept of Ophthalmology for her valuable advice, comments and constant encouragement for the completion of this study. -
Pupils and Near Vision
PUPILS AND NEAR VISION Akilesh Gokul PhD Research Fellow Department of Ophthalmology Iris Anatomy Two muscles: • Radially oriented dilator (actually a myo-epithelium) - like the spokes of a wagon wheel • Sphincter/constrictor Pupillary Reflex • Size of pupil determined by balance between parasympathetic and sympathetic input • Parasympathetic constricts the pupil via sphincter muscle • Sympathetic dilates the pupil via dilator muscle • Response to light mediated by parasympathetic; • Increased innervation = pupil constriction • Decreased innervation = pupil dilation Parasympathetic Pathway 1. Three major divisions of neurons: • Afferent division 2. • Interneuron division • Efferent division Near response: • Convergence 3. • Accommodation • Pupillary constriction Pupil Light Parasympathetic – Afferent Pathway 1. • Retinal ganglion cells travel via the optic nerve leaving the optic tracts 2. before the LGB, and synapse in the pre-tectal nucleus. 3. Pupil Light Parasympathetic – Efferent Pathway 1. • Pre-tectal nucleus nerve fibres partially decussate to innervate both Edinger- 2. Westphal (EW) nuclei. • E-W nucleus to ipsilateral ciliary ganglion. Fibres travel via inferior division of III cranial nerve to ciliary ganglion via nerve to inferior oblique muscle. 3. • Ciliary ganglion via short ciliary nerves to innervate sphincter pupillae muscle. Near response: 1. Increased accommodation Pupil 2. Convergence 3. Pupillary constriction Sympathetic pathway • From hypothalamus uncrossed fibres 1. down brainstem to terminate in ciliospinal centre -
Primary Pupillary Margin Cyst of the Iris Pigment Epithelium
Chinese Medicine, 2011, 2, 16-19 doi:10.4236/cm.2011.21003 Published Online March 2011 (http://www.SciRP.org/journal/cm) Primary Pupillary Margin Cyst of the Iris Pigment Epithelium Rosanna Dammacco1, Giovanni Giancipoli1, Silvana Guerriero1, Domenico Piscitelli2, Nicola Cardascia1 1Department of Ophthalmology and Otorhinolaryngology, Bari University, Bari, Italy 2Department of Pathological Anatomy, Bari University, Bari, Italy E-mail: [email protected] Received January 13, 2011; revised February 2, 2011; accepted February 10, 2011 Abstract Purpose: Description of a patient with a solitary cyst of the pupillary margin iris pigment epithelium (IPE). Methods: A 63-year-old man referred a suspected iris-ciliary body melanoma in his left eye. Based on both clinical examination and ultrasound biomicroscopy, melanoma was considered unlikely. Surgery was under- taken to correct recurrent deterioration of vision due to movement of the lesion across the visual axis. Results: The lesion was excised completely. Ultrasound biomicroscopy and histopathological examination ruled out melanoma and allowed a final diagnosis of primary pupillary margin cyst of the IPE, characterized of pig- mented epithelium, with no connective tissue or vessels. No recurrences or fresh lesions appeared during a one-year follow-up. Conclusions: Primary epithelial iris cysts are usually benign. Treatment is required only in symptomatic patients and those with an uncertain diagnosis. Ultrasound biomicroscopy is indispensable to confirm the clinical diagnosis, follow the clinical course and intervene if surgery is required. Keywords: Melanoma, Iris Pigment Epithelium, Pupillary Cyst, Surgical Excision, Ultrasound Biomicroscopy 1. Introduction This paper describes a case of symptomatic primary central IPE cyst initially mistaken for an iris melanoma. -
Nomina Histologica Veterinaria, First Edition
NOMINA HISTOLOGICA VETERINARIA Submitted by the International Committee on Veterinary Histological Nomenclature (ICVHN) to the World Association of Veterinary Anatomists Published on the website of the World Association of Veterinary Anatomists www.wava-amav.org 2017 CONTENTS Introduction i Principles of term construction in N.H.V. iii Cytologia – Cytology 1 Textus epithelialis – Epithelial tissue 10 Textus connectivus – Connective tissue 13 Sanguis et Lympha – Blood and Lymph 17 Textus muscularis – Muscle tissue 19 Textus nervosus – Nerve tissue 20 Splanchnologia – Viscera 23 Systema digestorium – Digestive system 24 Systema respiratorium – Respiratory system 32 Systema urinarium – Urinary system 35 Organa genitalia masculina – Male genital system 38 Organa genitalia feminina – Female genital system 42 Systema endocrinum – Endocrine system 45 Systema cardiovasculare et lymphaticum [Angiologia] – Cardiovascular and lymphatic system 47 Systema nervosum – Nervous system 52 Receptores sensorii et Organa sensuum – Sensory receptors and Sense organs 58 Integumentum – Integument 64 INTRODUCTION The preparations leading to the publication of the present first edition of the Nomina Histologica Veterinaria has a long history spanning more than 50 years. Under the auspices of the World Association of Veterinary Anatomists (W.A.V.A.), the International Committee on Veterinary Anatomical Nomenclature (I.C.V.A.N.) appointed in Giessen, 1965, a Subcommittee on Histology and Embryology which started a working relation with the Subcommittee on Histology of the former International Anatomical Nomenclature Committee. In Mexico City, 1971, this Subcommittee presented a document entitled Nomina Histologica Veterinaria: A Working Draft as a basis for the continued work of the newly-appointed Subcommittee on Histological Nomenclature. This resulted in the editing of the Nomina Histologica Veterinaria: A Working Draft II (Toulouse, 1974), followed by preparations for publication of a Nomina Histologica Veterinaria. -
I. Multiple Mechanisms of Accommodation A. Variable Axial Length B
Mechanics, Aging and Neurological Control of accommodation: I. Multiple Mechanisms of Accommodation A. Variable axial length B. Corneal Power C. Lenticular power D. Pupil size E. Lenticular refractive index gradient (isoindical surfaces) II. Anatomy A. Lens B. Capsule C. Zonules D. Ciliary Body E. Index gradient III. Autonomic innervation IV. Amplitude of accommodation and age A. Functional presbyopia B. Absolute presbyopia C. Treatment Bifocals Monovision Surgically implanted prosthesis Course title - (VS217) Oculomotor functions and neurology Instructor - Clifton Schor GSI: James O’Shea, Michael Oliver & Aleks Polosukhina Schedule of lectures, exams and laboratories : Lecture hours 10-11:30 Tu Th; 5 min break at 11:00 Labs Friday the first 3 weeks Examination Schedule : Quizes: January 29; February 28 Midterm: February 14: Final March 13 Power point lecture slides are available on a CD Resources: text books, reader , website, handouts Class Website: Reader. Website http://schorlab.berkeley.edu Click courses 117 class page name VS117 password Hering,1 First Week: read chapters 16-18 See lecture outline in syllabus Labs begin this Friday, January 25 Course Goals Near Response - Current developments in optometry Myopia control – environmental, surgical, pharmaceutical and genetic Presbyopia treatment – amelioration and prosthetic treatment Developmental disorders (amblyopia and strabismus) Reading disorders Ergonomics- computers and sports vision Virtual reality and personal computer eye-ware Neurology screening- Primary care gate keeper neurology, systemic, endocrines, metabolic, muscular skeletal systems. Mechanics, Aging and Neurological Control of accommodation : I. Five Mechanisms of Accommodation A. Variable axial length B. Corneal Power and astigmatism C. Lenticular power D. Pupil size & Aberrations E. Lenticular refractive index gradient (isoindical surfaces) II. -
Posterior Uveal (Ciliary Body and Choroidal) Melanoma Leslie T
Posterior Uveal (Ciliary Body and Choroidal) Melanoma Leslie T. L. Pham, MD, Jordan M. Graff, MD, and H. Culver Boldt, MD July 27, 2010 Chief Complaint: 31-year-old man with "floaters and blurry vision" in the right eye (OD). History of Present Illness: In August 2007, a healthy 31-year-old truck driver from Nebraska started noticing floaters in his right eye. The floaters gradually worsened and clouded his central vision. His family doctor tried changing his blood pressure medications, but this did not help. He later saw an ophthalmologist in his home state who told him there was a "mass" in his right eye. He was referred to the University of Iowa Department of Ophthalmology and Visual Sciences. Past Ocular History: The patient has had no prior eye surgery or trauma. Past Medical History: The patient reports prior excision of a benign skin nevus. He also has hypertension. Medications: Metoprolol and triamterene/hydrochlorothiazide Family History: The patient’s mother has a history of neurofibromatosis. His father had an enucleation for an "eye cancer" and subsequently died due to metastatic spread of the cancer. His grandmother had skin melanoma. Social History: The patient lives in Nebraska with his wife and child. He has never smoked and only drinks on "special occasions". Review of Systems: Negative, except as noted above. Ocular Examination: General: Well-developed, well-nourished Caucasian man in a pleasant mood Skin: Several scattered macules and papules on the trunk and all four extremities Distance visual acuity (without correction): o 20/60-2 OD o 20/20 OS Near acuity (without correction) o 20/30 OD o 20/20 OS Ocular motility: Full OU. -
Ophthalmic Pathology and Oncology A) Pathology
Ophthalmic pathology and oncology Objective Understanding the pathophysiology and oncology of the eye and in systemic diseases and their presentations. Differentiation of benign and malignant eye diseases, understanding the pathology and examination techniques with focus on the main risk factors of the disease. Recognising signs and symptoms of the disease with diagnostic tests at the slit lamp as well as functional and structural analysis. Management of presentation, including various therapeutic options (medical and surgical) and follow-up. Psychology and management of patients presenting with a potentially blinding and life-threatening disease. A) Pathology Anatomy and pathophysiology of: -Ocular anatomy and histology of the major structures of the eye and its adnexa: • Conjunctiva • Cornea • Sclera • Anterior chamber • Posterior chamber • Iris • Ciliary body • Lens • Vitreous • Retina and retinal pigment epithelium • Choroid • Optic nerve • Visual pathway • Eyelids • Extraocular muscles • Lacrimal system • Orbit Disease process • Congenital anomaly • Choristoma versus hamartoma Inflammation • Acute versus chronic • Focal versus diffuse • Granulomatus versus nongranulomatous Degeneration (includes dystrophy) Neoplasia • Benign versus malignant • Epithelial versus soft tissue versus haematopoietic -Basic pathophysiology of the common disease processes of the eye and its adnexa, and identify the major histologic findings: a. Degeneration (e.g., pterygium, keratoconus) b. Dystrophy (e.g., Fuchs’ dystrophy, TGFBI-associated dystrophies) c. Infection (e.g., fungal keratitis, bacterial endophthalmitis) d. Inflammation (e.g., chalazion, idiopathic orbital inflammation) e. Neoplasm and proliferation (e.g., basal and squamous cell carcinoma, uveal melanoma, retinoblastoma) - Pathophysiology and identify the major histologic findings of common diseases of the eye (e.g., keratitis, exfoliation syndrome, corneal and retinal dystrophies and degenerations, frequent neoplasms, oculoplastics, cornea, glaucoma, retina, ophthalmic oncology). -
Eye External Anatomy of Eye Accessory Structures
4/22/16 Eye Bio 40B Dr. Kandula External Anatomy of Eye Accessory Structures l Eyebrows l Levator Palpebrae Superioris - opens eye l Eyelashes l Ciliary glands – modified sweat glands l Small sebaceous glands l Sty is inflamed ciliary glands or small sebaceous glands 1 4/22/16 Terms: Lacrimal gland and duct Surface of eye Lacrimal puncta Lacrimal sac Nasolacrimal duct Nasal cavity Tears / Lacrimal fluid l a watery physiologic saline, with a plasma-like consistency, l contains the bactericidal enzyme lysozyme; l it moistens the conjunctiva and cornea, l provides nutrients and dissolved O2 to the cornea. Extrinsic Muscles of the Eye: Lateral/medial rectus Important to know Superior/inferior rectus actions and nerve Superior/inferior oblique supply in table 2 4/22/16 Extrinsic Eye Muscles • Eye movements controlled by six extrinsic eye muscles Four recti muscles § Superior rectus – moves eyeball superiorly supplied by Cranial Nerve III § Inferior rectus - moves eyeball inferiorly supplied by Cranial Nerve III § Lateral rectus - moves eyeball laterally supplied by Cranial Nerve VI § Medial rectus - moves eyeball medially supplied by Cranial Nerve III Extrinsic Eye Muscles Two oblique muscles rotate eyeball on its axis § Superior oblique rotates eyeball inferiorly and laterally and is supplied by Cranial Nerve IV § Inferior oblique rotates superiorly and laterally and is supplied by Cranial Nerve III Convergence of the Eyes l Binocular vision in humans has both eyes looking at the same object l As you look at an object close to your face, -
Localization and Characterization of Substance P Binding Sites in Rat and Rabbit Eyes
Investigative Ophthalmology & Visual Science, Vol. 32, No. 6, May 1991 Copyright © Association for Research in Vision and Ophthalmology Localization and Characterization of Substance P Binding Sites in Rat and Rabbit Eyes Philippe Denis,*t Veronique Fardin4 Jean-Philippe Nordmann,t Pierre-Paul Elena,§ Laurent Laroche,-(- Henri Saraux,t and William Rostene* Specific and high-affinity binding sites for Substance P (SP) were found in eyes from albino rabbits and rats using an in vitro autoradiographic method with l2SI-Bolton Hunter SP (BHSP). Autoradiograms were generated by apposing 10-20/im-thick cryostat eye sections to 3H-Hyperfilm or liquid emulsion and quantified by means of image-analysis procedures. Kinetic studies showed that equilibrium was reached after a 75-min incubation at room temperature. In rat retina, specific binding corresponding to approximately 90% of total binding, was reversible, of high affinity (dissociation constant [Kd], 0.13 ± 0.02 nM). Half-time for dissociation of 125I-BHSP was about 15 min. I) n la be led SP and the two neurokinins (NK) A and B competed in a concentration-dependent manner for retinal sites labeled by 125I-BHSP with the following order of potencies: SP > NKA > NKB, in agreement with a pharmaco- logic profile of a SP receptor site. In both species, specific binding was found in the iris sphincter muscle, choroid, and retina. In rats, detectable amounts of SP-binding sites were also expressed in the corneal epithelium and iridial stroma. Quantitative analysis of the autoradiograms revealed that the highest densities of 125I-BHSP binding sites were localized in the iris sphincter muscle in rabbits and the inner retina in rats. -
Presynaptic Effects of Botulinum Toxin Type a on the Neuronally Evoked Response of Albino and Pigmented Rabbit Iris Sphincter and Dilator Muscles
Presynaptic Effects of Botulinum Toxin Type A on the Neuronally Evoked Response of Albino and Pigmented Rabbit Iris Sphincter and Dilator Muscles Hitoshi Ishikawa,* Yoshihisa Mitsui,* Takeshi Yoshitomi,* Kimiyo Mashimo,* Shigeru Aoki,† Kazuo Mukuno† and Kimiya Shimizu* *Department of Ophthalmology, Kitasato University, School of Medicine, Sagamihara, Japan; †Department of Orthoptics and Visual Science, Kitasato University, School of Allied Health Sciences, Sagamihara, Japan Purpose: To investigate the effects of botulinum toxin type A (botulinum A toxin) on the autonomic and other nonadrenergic, noncholinergic nerve terminals. Methods: The effects of botulinum A toxin on twitch contractions evoked by electrical field stimulation (EFS) were studied in isolated albino and pigmented rabbit iris sphincter and di- lator muscles using the isometric tension recording method. Results: Botulinum A toxin inhibited the fast cholinergic and slow substance P-ergic compo- nent of the contraction evoked by EFS in the rabbit iris sphincter muscle without affecting the response to carbachol and substance P. These inhibitory effects were more marked in the albino rabbit than in the pigmented rabbit. Botulinum A toxin (150 nmol/L) did not affect the twitch contraction evoked by EFS in the rabbit iris dilator muscle. Conclusions: These data indicated that botulinum A toxin may inhibit not only the acetyl- choline release in the cholinergic nerve terminals, but also substance P release from the trigeminal nerve terminals of the rabbit iris sphincter muscle. However, the neurotoxin has little effect on the adrenergic nerve terminals of the rabbit iris dilator muscle. Furthermore, the botulinum A toxin binding to the pigment melanin appears to influence the response quantitatively in the two types of irides.