Vernal keratoconjunctivitis

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| Vernal keratoconjunctivitis | |
|---|---|
| |
| Synonyms | Spring catarrh, warm weather conjunctivitis |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Itching, redness, tearing, photophobia, discharge |
| Complications | Corneal ulcer, vision loss |
| Onset | Typically in childhood |
| Duration | Chronic, often resolves after puberty |
| Types | N/A |
| Causes | Allergic reaction |
| Risks | Atopy, family history |
| Diagnosis | Clinical diagnosis, slit lamp examination |
| Differential diagnosis | Atopic keratoconjunctivitis, giant papillary conjunctivitis, allergic conjunctivitis |
| Prevention | N/A |
| Treatment | Antihistamines, mast cell stabilizers, topical corticosteroids |
| Medication | N/A |
| Prognosis | N/A |
| Frequency | More common in tropical and subtropical regions |
| Deaths | N/A |
Vernal keratoconjunctivitis (VKC) is a chronic, bilateral inflammation of the conjunctiva and cornea. It is a form of allergic conjunctivitis that primarily affects children and young adults, particularly males, and is more prevalent in warm, dry climates.
Signs and Symptoms[edit]
VKC is characterized by intense itching, photophobia, tearing, and a thick, ropy discharge. Patients often experience a burning sensation and a feeling of a foreign body in the eye. The condition is typically seasonal, with exacerbations in the spring and summer months.
Conjunctival Changes[edit]
The conjunctiva may exhibit papillae on the upper tarsal conjunctiva, which can become large and cobblestone-like. Limbal papillae may also be present, often associated with Horner-Trantas dots, which are collections of degenerated epithelial cells and eosinophils.
Corneal Involvement[edit]
Corneal involvement can lead to keratitis, with the potential for corneal ulceration and pannus formation. In severe cases, shield ulcers may develop, which can significantly impact vision.
Pathophysiology[edit]
VKC is an IgE-mediated hypersensitivity reaction. The condition involves a complex interplay of mast cells, eosinophils, and T-lymphocytes. The release of inflammatory mediators such as histamine and cytokines contributes to the symptoms and tissue changes observed in VKC.
Diagnosis[edit]
Diagnosis is primarily clinical, based on the characteristic signs and symptoms. A detailed patient history and examination of the conjunctiva and cornea are essential. In some cases, conjunctival scrapings may be performed to identify eosinophils.
Management[edit]
Management of VKC involves avoiding known allergens and using pharmacological treatments to control symptoms. Topical antihistamines, mast cell stabilizers, and nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used. In more severe cases, topical corticosteroids or immunomodulatory agents such as cyclosporine may be necessary.
Prognosis[edit]
The prognosis for VKC is generally good, with most patients experiencing a reduction in symptoms as they age. However, ongoing management is often required to prevent complications and maintain quality of life.
See also[edit]
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