Exudative Retinitis (Coats Disease)
- PMID: 32809517
- Bookshelf ID: NBK560682
Exudative Retinitis (Coats Disease)
Excerpt
Coats disease is an idiopathic ocular condition characterized by retinal telangiectasia, aneurysms, and exudation. George Coats first described it in 1908 as a unilateral condition with retinal exudation and telangiectasia in male children. Later, Theodor von Leber described a similar case with telangiectatic and aneurysmal vessels without subretinal exudation. This condition was later known as Leber multiple miliary aneurysms. It was identified as an earlier disease process of Coats disease. Subsequently, Shields et al. defined Coats disease as ‘idiopathic retinal telangiectasia associated with exudation and frequent exudative retinal detachment with no signs of retinal or vitreal traction.’
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Sections
- Continuing Education Activity
- Introduction
- Etiology
- Epidemiology
- Pathophysiology
- Histopathology
- History and Physical
- Evaluation
- Treatment / Management
- Differential Diagnosis
- Staging
- Prognosis
- Complications
- Deterrence and Patient Education
- Enhancing Healthcare Team Outcomes
- Review Questions
- References
References
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- Jones JH, Kroll AJ, Lou PL, Ryan EA. Coats' disease. Int Ophthalmol Clin. 2001 Fall;41(4):189-98. - PubMed
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- Shields JA, Shields CL, Honavar SG, Demirci H. Clinical variations and complications of Coats disease in 150 cases: the 2000 Sanford Gifford Memorial Lecture. Am J Ophthalmol. 2001 May;131(5):561-71. - PubMed
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- Shienbaum G, Tasman WS. Coats disease: a lifetime disease. Retina. 2006 Apr;26(4):422-4. - PubMed
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- Shields JA, Shields CL, Honavar SG, Demirci H, Cater J. Classification and management of Coats disease: the 2000 Proctor Lecture. Am J Ophthalmol. 2001 May;131(5):572-83. - PubMed
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