Conjunctivitis Alergic

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    Conjunctivitis, Allergic

    Author: Parag A Majmudar, MD, Fellowship Co-Director, Department of Ophthalmology,

    Cornea and Refractive Surgery Service, Assistant Professor, Rush-Presbyterian-St Luke's

    Medical CenterContributor Information and Disclosures

    Updated: Aug 4, 2010

    Print This Email This

    Overview Differential Diagnoses & Workup Treatment & Medication Follow-up References Keywords

    Introduction

    Background

    Immunologic reactions of conjunctiva and cornea

    The ocular surface may exhibit a wide variety of immunologic responses that may result in

    conjunctival and corneal inflammation. In the Gell and Coombs classification system for

    various immunologic hypersensitivity reactions, 5 classes of reactions are recognized.

    Type I (immediate) hypersensitivity reactions occur when a sensitized individual comes in

    contact with a specific antigen. Immunoglobulin E (IgE) has a strong affinity for mast cells,

    and the cross-linking of 2 adjacent IgE molecules by the antigen triggers mast cell

    degranulation. This, in turn, causes the release of various preformed and newly formed

    mediators of the inflammatory cascade, including histamine, tryptase, chymase, heparin,

    chondroitin sulfate, prostaglandins, thromboxanes, and leukotrienes. These various

    inflammatory mediators, together with various chemotactic factors, result in increased

    vascular permeability and migration of eosinophils and neutrophils. The principal ocular type

    I hypersensitivity reaction is allergic conjunctivitis, which is discussed in further detail in this

    article.

    Type II hypersensitivity reactions are autoimmune reactions and may be complement

    mediated. These reactions may be the underlying cause of various ocular conditions, such as

    cicatricial pemphigoid and Mooren ulcer.

    Type III hypersensitivity reactions result in antigen-antibody immune complexes, whichdeposit in tissues and cause inflammation. Classic type III reaction systemically is the Arthus

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    reaction, and ocular type III hypersensitivity reactions include Stevens-Johnson syndrome

    and marginal infiltrates of the cornea. Corneal immune (Wesley) rings are also an example of

    type III reactions.

    Type IV hypersensitivity reactions, also known as cell-mediated immunity, are mediated by T

    lymphocytes. While type I reaction is immediate hypersensitivity, this reaction is also knownas delayed-type hypersensitivity, since its onset is generally after 48 hours. Type IV

    hypersensitivity reactions imply immunocompetence on the part of the individual since an

    intact immune system is required to mount the cell-mediated response. Ocular examples of

    type IV hypersensitivity include phlyctenular keratoconjunctivitis, corneal allograft rejection,

    contact dermatitis, and drug allergies.

    This section focuses primarily on the major type I hypersensitivity reactions involving the

    conjunctiva, more commonly referred to as allergic conjunctivitis.

    Types of allergic conjunctivitis

    Allergic conjunctivitis may be divided into 5 major subcategories. Seasonal allergic

    conjunctivitis (SAC) and perennial allergic conjunctivitis (PAC) are commonly grouped

    together. Vernal keratoconjunctivitis (VKC),atopic keratoconjunctivitis(AKC), andgiant

    papillary conjunctivitis(GPC) constitute the remaining subtypes of allergic conjunctivitis.

    Pathophysiology

    Seasonal and perennial allergic conjunctivitis

    Since conjunctiva is a mucosal surface similar to the nasal mucosa, the same allergens thattrigger allergic rhinitis may be involved in the pathogenesis of allergic conjunctivitis.

    Common airborne antigens, including pollen, grass, and weeds, may provoke the symptoms

    of acute allergic conjunctivitis, such as ocular itching, redness, burning, and tearing. The

    main distinction between SAC and PAC, as implied by the name, is the timing of symptoms.

    Individuals with SAC typically have symptoms of acute allergic conjunctivitis for a defined

    period of time, that is, in spring, when the predominant airborne allergen is tree pollen; in

    summer, when the predominant allergen is grass pollen; or in fall, when the predominant

    allergen is weed pollen. Typically, persons with SAC are symptom-free during the winter

    months in cooler climates because of the decreased airborne transmission of these allergens.

    In contrast, individuals with PAC may have symptoms that last the whole year; thus, PAC

    may not be caused exclusively by seasonal allergens, although they may play a role. Other

    common household allergens, such as dust mite, cockroaches, and pet dander, may be

    responsible for the symptoms of PAC.

    Vernal keratoconjunctivitis

    VKC is a chronic bilateral inflammation of the conjunctiva, commonly associated with a

    personal and/or family history of atopy. More than 90% of patients with VKC exhibit one or

    more atopic conditions, such as asthma, eczema, or seasonal allergic rhinitis.

    Atopic keratoconjunctivitis

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    AKC is a bilateral inflammation of conjunctiva and eyelids, which has a strong association

    with atopic dermatitis. It is also a type I hypersensitivity disorder with many similarities to

    VKC, yet AKC is distinct in a number of ways.

    In 1953, Hogan first described the association between atopic dermatitis and conjunctival

    inflammation.1

    He reported 5 cases of conjunctival inflammation in male patients with atopicdermatitis.

    1Atopic dermatitis is a common hereditary disorder that usually has its onset in

    childhood; symptoms may regress with advancing age. Approximately 3% of the population

    is afflicted with atopic dermatitis, and, of these, approximately 25% have ocular involvement.

    Giant papillary conjunctivitis

    GPC is an immune-mediated inflammatory disorder of superior tarsal conjunctiva. As the

    name implies, the primary finding is the presence of "giant" papillae, which are typically

    greater than 0.3 mm in diameter. It is believed that GPC represents an immunologic reaction

    to a variety of foreign bodies, which may cause prolonged mechanical irritation to the

    superior tarsal conjunctiva. Although contact lenses (hard and soft) are the most commonirritant, ocular prostheses, extruded scleral buckles, and exposed sutures following previous

    surgical intervention may precipitate GPC.

    Frequency

    United States

    Allergic conjunctivitis occurs very frequently and is seen most commonly in areas with high

    seasonal allergens.

    Mortality/Morbidity

    Allergic conjunctivitis rarely causes any visual loss.

    Race

    VKC occurs predominantly in areas with tropical and temperate climates, such as the

    Mediterranean, the Middle East, and Africa.

    The limbal form of VKC commonly occurs in dark-skinned individuals from Africa and

    India.

    Sex

    VKC has a significant male preponderance.

    Age

    VKC typically affects young males with onset generally in the first decade and with duration

    up to one decade. Its symptoms usually peak prior to the onset of puberty and then subside.

    Clinical

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    History

    Seasonal and perennial allergic conjunctivitis

    Diagnosis of allergic conjunctivitis generally is made by taking a thorough history and by

    careful clinical observation.

    Important features of history include a personal or family history of atopic disease, such as

    allergic rhinitis, bronchial asthma, and/or atopic dermatitis. Perhaps the most important

    feature in the clinical history is the symptom of itching. Without itching, the diagnosis of

    allergic conjunctivitis is suspect.

    Vernal keratoconjunctivitis

    As with other allergic or type I hypersensitivity disorders, itching is the most important and

    most common symptom.

    Other commonly reported symptoms are photophobia, foreign body sensation, tearing, and

    blepharospasm.

    Ocular signs of VKC commonly are seen in the cornea and conjunctiva. In contrast to AKC,

    the eyelid skin usually is not involved.

    Atopic keratoconjunctivitis

    In contrast to the symptoms of VKC, the symptoms in AKC are perennial. However, there

    may be seasonal variation with worsening symptoms during winter months.

    The single most common symptom is bilateral itching of the eyelids, but watery discharge,

    redness, photophobia, and pain may be associated.

    Giant papillary conjunctivitis

    Primary symptoms in GPC are ocular itching with a mucoid or ropy discharge, very similar to

    that seen in VKC.

    Another symptom may be a persistent foreign body sensation when using contact lenses,

    resulting in an inability to wear contact lenses for the desired length of time.

    Physical

    Seasonal and perennial allergic conjunctivitis

    Classic signs of allergic conjunctivitis include injection of conjunctival vessels as well as

    varying degrees of chemosis (conjunctival edema) and eyelid edema.

    The conjunctiva often has a milky appearance due to obscuration of superficial blood vessels

    by edema within the substantia propria of the conjunctiva. Edema is generally believed to be

    the direct result of increased vascular permeability caused by release of histamine fromconjunctival mast cells.

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    Vernal keratoconjunctivitis

    VKC may be subdivided into 2 varieties, as follows: palpebral and limbal. The classic

    conjunctival sign in palpebral VKC is the presence of giant papillae. They most commonly

    occur on the superior tarsal conjunctiva; usually, the inferior tarsal conjunctiva is unaffected.

    Giant papillae assume a flattop appearance, which often is described as "cobblestonepapillae." In severe cases, large papillae may cause mechanical ptosis.

    A ropy mucous discharge may be present, which commonly is associated with tarsal papillae.

    Large numbers of eosinophils are present in the discharge.

    The limbal form of VKC commonly occurs in dark-skinned individuals, such as those from

    Africa or India. As the name implies, papillae tend to occur at the limbus and have a thick

    gelatinous appearance. They commonly are associated with multiple white spots (Horner-

    Trantas dots), which are collections of degenerated epithelial cells and eosinophils. Horner-

    Trantas dots are transient, with each appearance rarely lasting more than 1 week.

    While corneal vascularization is rare, the cornea may be affected in a variety of ways.

    Punctate epithelial keratopathy (PEK) may be due to the toxic effect of inflammatory

    mediators released from the conjunctiva and may be a precursor of the characteristic shield

    ulcer, which is pathognomonic of VKC. As the areas of PEK coalesce, they may result in

    frank epithelial erosion resulting in shield ulcer, which is typically shallow with white

    irregular epithelial borders. Although the pathogenesis of shield ulcer is not well understood,

    a major factor in promoting development may be chronic mechanical irritation from the giant

    tarsal papillae. Some evidence suggests that the major basic protein released from eosinophils

    may promote ulceration.

    Another type of corneal involvement is vernal pseudogerontoxon, which is a degenerative

    lesion in the peripheral cornea resembling corneal arcus. Keratoconus may be seen in chronic

    cases, which may be associated with chronic eye rubbing.

    Atopic keratoconjunctivitis

    AKC may affect eyelid skin and lid margin, conjunctiva, cornea, and lens. Skin of the eyelids

    may exhibit eczematoid dermatitis with dry, scaly, and inflamed skin. Lid margins may show

    meibomian gland dysfunction and keratinization. Staphylococcal colonization of eyelid

    margins is very common and may result in blepharitis. Conjunctiva may show chemosis and

    typically a papillary reaction, which is more prominent in the inferior tarsal conjunctiva, incontrast to that seen in vernal keratoconjunctivitis.

    Hyperplasia of limbal regions may result in a gelatinous thickening, similar to the limbal

    variant of VKC, and Horner-Trantas dots also may be present, although rarely. Fibrosis or

    scarring of the conjunctiva may result in a shortened fornix or symblepharon formation with

    chronic inflammation. Corneal involvement ranges from punctate epithelial keratopathy early

    in the course of the disease, to neovascularization, stromal scarring, and possibly ulceration.

    There is a strong association between herpes simplex viral keratitis and AKC.

    Another corneal finding, which may be associated with AKC, is keratoconus, which may

    stem from chronic eye rubbing. Characteristic lenticular changes in AKC include anterior orposterior subcapsular cataract formation. Lens opacities are usually bilateral and present in

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    the second decade of life but progress very slowly. There may be an association with the

    long-term use of topical corticosteroids. Note that there is an increased incidence of retinal

    detachment following surgical removal of cataracts in patients with atopic dermatitis; the

    exact mechanism is unknown.

    Table. Major Differentiating Factors Between VKC and AKC

    Opentable in new window

    [CLOSE WINDOW]

    Table

    Characteristics VKC AKC

    Age at onset Generally presents at a younger age -

    Sex Males are affected preferentially. No sex predilection

    Seasonal variation Typically occurs during spring months Generally perennial

    Discharge Thick mucoid discharge Watery and clear discharge

    Conjunctival scarring - Higher incidence of

    conjunctival scarring

    Horner-Trantas dots Horner-Trantas dots and shield ulcers

    are commonly seen.

    Presence of Horner-Trantas

    dots is rare.

    Corneal neovascularization Not present Tends to develop deep

    corneal neovascularization

    Presence of eosinophils in

    conjunctival scraping

    Conjunctival scraping reveals

    eosinophils to a greater degree in VKC

    than in AKC.

    Presence of eosinophils is less

    likely.

    Characteristics VKC AKC

    Age at onset Generally presents at a younger age -

    Sex Males are affected preferentially. No sex predilection

    Seasonal variation Typically occurs during spring months Generally perennial

    Discharge Thick mucoid discharge Watery and clear discharge

    Conjunctival scarring - Higher incidence of

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    conjunctival scarring

    Horner-Trantas dots Horner-Trantas dots and shield ulcers

    are commonly seen.

    Presence of Horner-Trantas

    dots is rare.

    Corneal neovascularization Not present Tends to develop deep

    corneal neovascularization

    Presence of eosinophils in

    conjunctival scraping

    Conjunctival scraping reveals

    eosinophils to a greater degree in VKC

    than in AKC.

    Presence of eosinophils is less

    likely.

    Giant papillary conjunctivitis

    Examination of superior tarsal conjunctiva reveals the presence of large cobblestone papillae,which are generally 0.3 mm or greater in diameter and, in severe cases, may cause

    mechanical ptosis of the upper lid.

    In his original description of GPC in 1977, Allansmith described 3 zones of superior tarsal

    conjunctiva.2

    Zone 1 is located closest to the fornix and is the most inferior portion of the

    tarsal conjunctiva seen when the upper eyelid is everted. Zone 3 is located closest to the

    eyelid margin. Zone 2 is located between zone 1 and zone 3.

    Papillae typically associated with soft contact lensrelated GPC initially appear in zone 1 and

    progress toward zone 3, while those associated with rigid gas permeable contact lenses

    exhibit a reverse pattern, with zone 3 affected first. GPC associated with a localized irritant,such as an exposed suture or a filtering bleb, is typically localized to the area overlying these

    inciting lesions.

    Another clinical sign of GPC may be chronic bulbar conjunctival injection and inflammation

    due to prolonged and persistent use of contact lenses.