Atlas of Ophthalmology

Anterior Chamber

Brain and Optical Pathway

Congenital Syndromes, Malformations and Abnomalities

Glaucomas, Ocular Hypertension

Hypertensive Retinopathy

Iris and Ciliary Body

Lacrimal System

Neuro-Ophthalmology

Anatomy and Embryology

Angioid Streaks

Aquired Macular Diseases

Congenital Abnormalities and Syndromes

Diseases of Hematopoesis (see under Systemic Diseases)

Hereditary Degenerations and Dystrophies

Infections (see Systemic Diseases)

Retinal Detachment, Rhegmatogenous. Retinal Perforations, Breaks

Proliferative Vitreoretinopathy (PVR)

Proliferative Vitreoretinopathy (PVR), Classification

Proliferative Vitreoretinopathy (PVR), Preretinal Proliferation

Proliferative Vitreoretinopathy (PVR), Subretinal Proliferation

Case, Proliferative Vitreoretinopathy (PVR), Subretinal Proliferation

PVR, Pre- and Subretinal Proliferation, Early, Grade A

PVR, Subretinal Cell Cluster, Early, Histology

PVR, Subretinal Proliferation

PVR, Subretinal Proliferation, Attached Retina

PVR. Subretinal Proliferation

Proliferative Vitreoretinopathy (PVR), Vitreal Proliferation

PVR, Total Retinal Detachment

PVR,Total Retinal Detachment, Ultrasound

Rhegmatogenous Retinal Detachment

Surgical Procedures and Postoperative Cases

Toxic Retinopathies; see also Light Toxicitiy

Trauma (Injury)

Tumors, Neoplasma

Vascular Diseases (see also: Systemic Immunologic Diseases)

Strabismus, Ocular Motility Disorders

Systemic Diseases

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PVR, Pre- and Subretinal Proliferation, Early, Grade A

Diagnosis:	PVR, Pre- and Subretinal Proliferation, Early, Grade A
Comment to photo:	Preretinal pigmentation and subretinal white dots are caused by proliferating cells deriving from RPE
Author(s):	Machemer, Robert, M.D., Duke Univ. Medical School, Durham, NC, USA
ICD10-Code:	H35.21
Path:	Retina -> Retinal Detachment, Rhegmatogenous. Retinal Perforations, Breaks -> Proliferative Vitreoretinopathy (PVR) -> Proliferative Vitreoretinopathy (PVR), Subretinal Proliferation
Additional keywords:	retina
Image ID:	1551

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