Physical Address
304 North Cardinal St.
Dorchester Center, MA 02124
Recurrent corneal erosion (RCE) syndrome is a common clinical entity that can be frustrating to both patients (due to cyclical symptoms) and treating clinicians (due to difficulty in diagnosis and treatment).
Although most patients can be diagnosed based on history alone, certain patients will require a thorough ocular examination and additional diagnostic testing to make a diagnosis.
In general, the clinician should divide RCE patients into two groups to help with treatment recommendation: loss of basement membrane (traumatic etiology) versus abnormal material between basement membrane and epithelium (dystrophies and degenerations), respectively.
A commonly encountered entity, recurrent corneal erosion (RCE) syndrome was first described in 1872 by Hansen as “intermittent neuralgic vascular keratitis.” Characterized by repeated breakdown of the corneal epithelium due to dysfunction in the epithelial-stromal complex integrity, erosions can occur spontaneously or be associated with a prior corneal injury, certain corneal dystrophies, or systemic illnesses ( Table 21.1 ). The areas of denuded corneal epithelium reepithelialize, yet the process recurs in the future with another cycle of epithelial sloughing. Without the overlying corneal epithelium to protect the Bowman layer, the stroma is exposed in the eroded areas, leading to progressive damage and opacification of the stroma.
Primary |
Epithelial Dystrophy |
|
Bowman Layer Dystrophy |
|
Stromal Dystrophy |
|
Endothelial Dystrophy |
|
Secondary |
Trauma |
|
Degeneration |
|
Eyelid Pathology |
|
Postinfectious Keratitis |
|
Systemic Etiology |
|
Other |
|
Become a Clinical Tree membership for Full access and enjoy Unlimited articles
If you are a member. Log in here