Imaging of Pediatric Orbital Diseases
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AANP Teaching Rounds: Fausto J. Rodriguez MD Director, Clinical Neuropathology Service Professor of Pathology, Oncology and Ophthalmology Johns Hopkins University School of Medicine Disclosures • I have no relevant financial relationships to disclose Learning Objectives • Learning Objective #1: Outline the differential diagnosis of tumors of the ocular surface • Learning Objective #2: Recognize the spectrum of ocular infections relevant to ophthalmic pathology • Learning Objective #3: Recognize the morphologic features of the most common keratopathies and dystrophies Case 1 • 60-year-old woman with past medical history of hypertension, GERD, Atrial fibrillation and DVT • Autopsy: acute pulmonary hemorrhage, aortopulmonary fistula, and aortic dissection • No clinical history of eye disease Findings • Fuchs Dystrophy • Fuchs Adenoma Case 1 Fuchs Endothelial Corneal Dystrophy • Most common corneal dystrophy in the US • Corneal edema in ~5th-6th decade of life • Primary defect in corneal endothelium • Relatively easy clinical and pathologic diagnosis • PAS stain very useful in equivocal cases Fuchs adenoma • Benign tumor possibly developing from non-pigmented ciliary epithelium • Age related • Typically incidental at autopsy, but may rarely cause iris protrusion, shallowing of anterior chamber or glaucoma Case 2 • 54-year-old man with visual loss Masson Trichrome PAS Congo Red Case 2 Granular Corneal Dystrophy • Visual loss late in life • May recur in grafts after transplantation • Autosomal dominant inheritance • Transforming growth factor -
Commentary on the Masquerades of A
perim Ex en l & ta a l ic O p in l h t C h f Journal of Clinical & Experimental a o l m l a o n l r o Chua, J Clin Exp Ophthalmol 2016, 7:2 g u y o J Ophthalmology 10.4172/2155-9570.1000543 ISSN: 2155-9570 DOI: Commentary Open Access Commentary on the Masquerades of a Childhood Ciliary Body Medulloepithelioma: A Case of Chronic Uveitis, Cataract, and Secondary Glaucoma Jocelyn Chua* Eye Specialist Clinic, 290 Orchard Road, Singapore *Corresponding author: Dr Jocelyn Chua, Eye Specialist Clinic, 290 Orchard Road, #06-01 to 05, 238859, Singapore; Tel: +65 96897919; Email: [email protected], [email protected] Received date: February 09, 2016; Accepted date: April 20, 2016; Published date: April 25, 2016 Copyright: © 2016 Chua J. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Commentary Ciliary body medulloepithelioma is the commonest ciliary body tumor in childhood. The term “medulloepithelioma”, coined by "The masquerades of a childhood ciliary body medulloepithelioma: Grinker in 1931, best describes the origin of the tumor from the A case of chronic uveitis, cataract and secondary glaucoma" by Chua et primitive medullary epithelium located along the inner layer of the al. [1] is a case report of a healthy two year old boy who presented with optic cup. This undifferentiated medullary epithelium forms the non- a unilateral cataract, anterior uveitis and glaucoma after an innocuous pigmented ciliary body epithelium in the later years of development. -
The Uveo-Meningeal Syndromes
ORIGINAL ARTICLE The Uveo-Meningeal Syndromes Paul W. Brazis, MD,* Michael Stewart, MD,* and Andrew G. Lee, MD† main clinical features being a meningitis or meningoenceph- Background: The uveo-meningeal syndromes are a group of disorders that share involvement of the uvea, retina, and meninges. alitis associated with uveitis. The meningeal involvement is Review Summary: We review the clinical manifestations of uveitis often chronic and may cause cranial neuropathies, polyra- and describe the infectious, inflammatory, and neoplastic conditions diculopathies, and hydrocephalus. In this review we define associated with the uveo-meningeal syndrome. and describe the clinical manifestations of different types of Conclusions: Inflammatory or autoimmune diseases are probably uveitis and discuss the individual entities most often associ- the most common clinically recognized causes of true uveo-menin- ated with the uveo-meningeal syndrome. We review the geal syndromes. These entities often cause inflammation of various distinctive signs in specific causes for uveo-meningeal dis- tissues in the body, including ocular structures and the meninges (eg, ease and discuss our evaluation of these patients. Wegener granulomatosis, sarcoidosis, Behc¸et disease, Vogt-Koy- anagi-Harada syndrome, and acute posterior multifocal placoid pig- ment epitheliopathy). The association of an infectious uveitis with an acute or chronic meningoencephalitis is unusual but occasionally the eye examination may suggest an infectious etiology or even a The uveo-meningeal syndromes are a specific organism responsible for a meningeal syndrome. One should consider the diagnosis of primary ocular-CNS lymphoma in heterogeneous group of disorders that share patients 40 years of age or older with bilateral uveitis, especially involvement of the uvea, retina, and meninges. -
Ocular Involvement in AIDS
Eye (1988) 2,496-505 Ocular Involvement in AIDS ALLAN E. KREIGER, and GARY N. HOLLAND, Los Angeles, USA The acquired immunodeficiency syndrome roaneurysms, and intraretinal microvascular (AIDS) is no longer a rare disease afflicting abnormalities. Autopsy studies of AIDS only a small segment of the world popula patients indicate that capillary changes in the tion. It has been recognised to occur in most retina are almost always present. These countries of the world; and, as of October, include swelling of endothelial cells, thicken 1987, there had been over 1000 cases ing of the basal lamina, degeneration and loss reported in the United Kingdom. I Despite of pericytes, and narrowing of capillary scientific determination of the causitive lumens. IS The pathogenetic mechanisms agent, better understanding of the behind these changes are not known, how pathogenesis of the clinical disease, and ever HIV has recently been shown to be pre clarification of the risk factors involved, the sent in retinal tissue. IS Viral (HIV-l) antigen epidemic continues to spread. As physicians, was found in the internal and external nuc we are destined to have to deal with the rav lear layers and the external plexiform layer as ages of AIDS increasingly in the future. well as in the capillary endothelial cells. Pos The first case reports of what became sibly, the endothelial infection results in known as AIDS appeared in 1981.2 Ophthal capillary alterations and occlusions. Another mic lesions were noted in the UCLA patients possibility is the deposition of circulating from the very beginning; they were reported immune complexes, which have arisen from by Holland and his associates in 1982.3 Since systemic infections, in the retinal capillaries. -
(Diktyoma) Presenting As a Perforated, Infected Eye
Br J Ophthalmol: first published as 10.1136/bjo.61.3.229 on 1 March 1977. Downloaded from British Journal of Ophthalmology, 1977, 61, 229-232 Medulloepithelioma (diktyoma) presenting as a perforated, infected eye MOHAMED A. VIRJI Central Pathology Laboratory, Ministry of Health, Dar-es-Salaam, Tanzania SUMMARY A case of embryonal medulloepithelioma (diktyoma) presenting with perforated infected eye in a 13-year-old Black African girl is described. The tumour mass occupied most of the deformed eye, and invasion of the sclera anteriorly was seen. There was no evidence of orbital or distant tumour involvement. It is suggested that with increasing age these tumours are more likely to show frankly malignant features. Medulloepithelioma (diktyoma) is a rare neoplasm anteriorly perforated left eye, with loss of cornea, of the eye which is characterised by slow growth and purulent discharge, and a fragmenting mass of local invasion and is composed of glandular, irregular brownish-grey tissue attached mainly to neural, and mesenchymal elements (Andersen, the superior and temporal portion of the eye and 1962). It presents even rarely as an infected perfor- extending into the posterior chamber. The infection ated eye with a fungating mass replacing the ocular was controlled with systemic antibiotics and the left copyright. contents. Soudakoff (1936) reported the case of a eye was enucleated. Radiological examination of 28-year-old Chinese who had a perforated eye with the skull showed no orbital involvement, and chest tumour mass completely filling it. This paper x-rays were normal. Postoperative recovery was reports the case of a young black African girl who uneventful. -
Primary Orbital Lymphoma – a Challenging Diagnosis
10.2478/AMB-2020-0030 PRIMARY ORBITAL LYMPHOMA – A CHALLENGING DIAGNOSIS St. Vylkanov1, K. Trifonova2, K. Slaveykov3, D. Dzhelebov2 1Department of Neurosurgery, Trakia University – Stara Zagora, Bulgaria 2Department of Ophthalmology, Trakia University – Stara Zagora, Bulgaria 3First Department of Internal Diseases and General Medicine, Trakia University – Stara Zagora, Bulgaria Abstract. Background and purpose: The occurrence of primary orbital lymphoma com- prises approximately 1% of non-Hodgkin’s lymphoma and 8% of extranodal lymphoma. The vast majority of orbital lymphomas are of B-cell origin, of which extranodal margin- al zone B-cell lymphoma is the most common subtype. The purpose of this paper was to present the diagnostic challenges in a case of orbital lymphoma. Case presentation: An 84- year -old woman with orbital tumour was operated on after a long period of inappropriate treatment. It was later diagnosed as B-cell lymphoma. Conclusion: Orbital lymphoma can be easily mistaken for another ocular disease due to the slowly progressing non-specific complaints of the patients. We should be alert to the possibility of this ocular diagnosis when we are presented with an elderly patient with proptosis. Key words: B-cell lymphoma, challenge, non-specific, elderly Corresponding author: K. Slaveykov, First Department of Internal Diseases and General Medicine, 11 Armeyska Street, 6000 Stara Zagora, Bulgaria, e-mail: [email protected] BACKGROUND phoid tissue type (MALT) (59%) is the most common subtype, followed by diffuse large B-cell lymphoma rbital lymphoma is reported as the most com- (23%), follicular lymphoma (9%), and mantle cell lym- mon malignant tumor of the ocular adnexa, phoma (5%) [18]. -
Retinoblastoma Simulators
Retinoblastoma: Atypical Presentation & Simulators Dr. Njambi Ombaba; Paediatric Ophthalmologist, University of Nairobi Objectives • To review of typical presentation of retinoblastoma • To understand the atypical presentation • To understand the Rb simulators Presentation of retinoblastoma Growth patterns Endophytic: Inner retina, vitreous mass, no overlying vessels, pseudohypopyon Exophytic: Outer retina, SR space mass, overlying vessels, RD Diffuse: No mass, signs of inflammation/ endophthalmitis Echogenic soft tissue mass Variable shadowing – calcification Persistent on reduced gain Heterogeneous – necrosis/ haemorrhage Floating debris- vitreous seeds, increased globulin MRI- • Pre-treatment staging T1- Hyper intense to vitreous T2-Hypo intense to vitreous T1:C+Gd- homo/ heterogeneous Enhancement: Choroid & AC ON involvement Hypo intense sclera- Normal Trilateral retinoblastoma CT SCAN Typically a mass of high density Usually calcified and moderately enhancing on iodinated contrast CT has a sensitivity of 81–96%, and a higher specificity for calcification detection However, delineation of intraocular soft-tissue detail is limited. Low sensitivity for ON invasion Atypical presentation Non calcified Retinoblastoma Calcification is key to diagnosis retinoblastoma US detects calcifications in 92–95% of positive cases Non-calcified retinoblastomas: 1. Tumefaction with irregular internal structure 2. Medium reflectivity 3. Typical signs of vascularity 4. Retinal detachment with part of the retinal surface destroyed. Rare, 2% of all -
Orbital Lymphoma Review of Literature
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) e-ISSN: 2279-0853, p-ISSN: 2279-0861.Volume 18, Issue 4 Ser. 1 (April. 2019), PP 05-09 www.iosrjournals.org Orbital Lymphoma Review of Literature Dr Rakesh Kumar MS1, Dr Priya Sinha MS2, Dr Nimish Kumar Singh MS3, Dr Abhay Kumar DNB4, Prof. Rajiv Gupta5 1Department of Ophthalmology 2Obsteritician and gynecologist 3Department of Ophthalmology 4Department of Pediatrics 5Department of Ophthalmology RIMS Ranchi Corresponding Author: Dr Rakesh Kumar MS Department of Ophthalmology Disclosure The authors have no financial interests in any of the products mentioned in the article. AIM: To discuss presentation, investigation, diagnosis and treatment of orbital lymphoma ----------------------------------------------------------------------------------------------------------------------------- ---------- Date of Submission: 20-03-2019 Date of acceptance: 06-04-2019 --------------------------------------------------------------------------------------------------------------------------------------- I. Background: Lymphoid tumours are the most common primary orbital malignancy in adults constituting about 10% of all orbital tumors1 and about 2% of all lymphomas.2 Lymphoma represents about 13% of primary malignant eyelid tumors.3 Orbital lymphoma may present as in localized form (orbit, lacrimal gland, lids, and conjunctiva) of systemic lymphoma . Majority of orbital lymphomas are non Hodgkin’s type and are seen primarily in adults in the 50 to 70 year age group. Orbital lymphoma can affect the conjunctiva, eyelid, and orbit/lacrimal gland as well as the nasolacrimal drainage system. The reported frequencies of involvement in these sites are the conjunctiva 20– 33%, orbit/lacrimal gland 46–74%, and eyelid 5–20%.4,5 Orbital lymphomas are usually unilateral but may involve both orbits and demonstrate a predilection for the lacrimal gland. Bilaterality is reported in 10–20% of cases. -
Intralesional Rituximab for Primary Iris Lymphoma
Letters Laboratories, Allergan, Inspire, Ista Pharmaceuticals, and LUX Biosciences; injection, the tumor shrank and completely disappeared on and having stock or stock options in Eyegate. No other disclosures were slitlamp, gonioscopic, and ultrasonographic biomicroscopic reported. examinations by 5 months (Figure, G-I). There were no ante- 1. Teichmann L. Das Saugader System. Leipzig, Germany: Engelmann; 1861:1-121. rior segment toxic effects or recurrence 8 months after the 2. Busacca A. Les vaisseaux lymphatiques de la conjonctive bulbaire humaine last injection and no evidence of systemic lymphoma based étudiés par la méthode des injections vitales de bleutripan. Arch d’opht. 1948; 8:10. on examination and fludeoxyglucose F 18 positron emission 3. Nakao S, Hafezi-Moghadam A, Ishibashi T. Lymphatics and tomography. lymphangiogenesis in the eye. J Ophthalmol. 2012;2012:783163. 4. Mihara M, Hara H, Araki J, et al. Indocyanine green (ICG) lymphography is Discussion | Intralesional rituximab injection is used success- superior to lymphoscintigraphy for diagnostic imaging of early lymphedema of fully to treat ocular lymphomas. Savino et al4 described 7 pa- the upper limbs. PLoS One. 2012;7(6):e38182. tients with adnexal MALT lymphomas, treated with 4 weekly 5. Rayes A, Oréfice F, Rocha H. Distribuição da rede linfática da conjuntiva bulbar humana normal, estudada através de injeções conjuntivais de azul de injections and followed up for more than 1 year, who had com- tripan a 1%. Arq Bras Oftalmol. 1980;43(5):188-200. plete remission (4 patients [57%]), partial response (2 pa- 6. Singh D. Conjunctival lymphatic system. J Cataract Refract Surg. 2003;29(4): tients [29%]), or no response (1 patient [14%]); the disease re- 632-633. -
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. -
Choroidal and Adnexal Extranodal Marginal Zone B-Cell
Eye (2013) 27, 828–835 & 2013 Macmillan Publishers Limited All rights reserved 0950-222X/13 www.nature.com/eye 1 2 1 CLINICAL STUDY Choroidal and P Loriaut , F Charlotte , B Bodaghi , D Decaudin3, V Leblond4, C Fardeau1, adnexal extranodal L Desjardins5, P Lehoang1 and N Cassoux5 marginal zone B-cell lymphoma: presentation, imaging findings, and therapeutic management in a series of nine cases Abstract Purpose To describe the clinical and Eye (2013) 27, 828–835; doi:10.1038/eye.2013.74; imaging presentation, pitfalls in the published online 19 April 2013 1Department of Ophthalmology, diagnosis of choroidal extranodal marginal Pitie´ -Salpe´ trie` re Hospital, zone B-cell lymphoma of mucosa-associated Keywords: choroid; extranodal marginal zone Paris, France lymphoid tissue (MALT), as well as the B-cell lymphoma of mucosa-associated therapeutic management and prognosis. lymphoid tissue; MALT 2 Department of Pathology, Methods A retrospective case review of nine Pitie´ -Salpe´ trie` re Hospital, Paris, France choroidal MALT lymphomas was performed. Initial clinical presentation and imaging Introduction 3Department of findings of these histologically confirmed Non-Hodgkin lymphoma (NHL) is a general Hematology, Institut Curie cases of lymphoma were analyzed. Treatment term for a large group of malignancies of Paris, Paris, France methods, time to diagnosis, systemic work- lymphoid tissue. Although it usually affects the up, and treatment prognosis were assessed. lymphatic system, extranodal sites are common 4Department of Hematology, Results Initial presentation was essentially and may involve almost all tissues. Although Pitie´ -Salpe´ trie` re Hospital, blurred vision. The features described on lymphoma of the ocular region is a relatively Paris, France examination were: anterior and posterior rare condition, NHL is the most common type scleritis, iridocyclitis, choroidal infiltration, and typically involves mucosa-associated 5 Department of Ophthalmic and exudative retinal detachment. -
Successful Treatment of Ciliary Body Medulloepithelioma with Intraocular
Stathopoulos et al. BMC Ophthalmology (2020) 20:239 https://doi.org/10.1186/s12886-020-01512-y CASE REPORT Open Access Successful treatment of ciliary body medulloepithelioma with intraocular melphalan chemotherapy: a case report Christina Stathopoulos*, Marie-Claire Gaillard, Julie Schneider and Francis L. Munier Abstract Background: Intraocular medulloepithelioma is commonly treated with primary enucleation. Conservative treatment options include brachytherapy, local resection and/or cryotherapy in selected cases. We report for the first time the use of targeted chemotherapy to treat a ciliary body medulloepithelioma with aqueous and vitreous seeding. Case presentation: A 17-month-old boy with a diagnosis of ciliary body medulloepithelioma with concomitant seeding and neovascular glaucoma in the right eye was seen for a second opinion after parental refusal of enucleation. Examination under anesthesia showed multiple free-floating cysts in the pupillary area associated with iris neovascularization and a subluxated and notched lens. Ultrasound biomicroscopy revealed a partially cystic mass adjacent to the ciliary body between the 5 and 9 o’clock meridians as well as multiple nodules in the posterior chamber invading the anterior vitreous inferiorly. Fluorescein angiography demonstrated peripheral retinal ischemia. Left eye was unremarkable. Diagnosis of intraocular medulloepithelioma with no extraocular invasion was confirmed and conservative treatment initiated with combined intracameral and intravitreal melphalan injections given according to the previously described safety-enhanced technique. Ciliary tumor and seeding totally regressed after a total of 3 combined intracameral (total dose 8.1 μg) and intravitreal (total dose 70 μg) melphalan injections given every 7–10 days. Ischemic retina was treated with cryoablation as necessary.