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Entropion

Entropion is an disorder characterized by the inward turning of the margin, most commonly the lower lid, which causes the eyelashes and to rub against the and , resulting in irritation, discomfort, and potential corneal damage. This condition primarily affects older adults, with a of approximately 2.1% in individuals over 60 years, and is more common in women and those of white ethnicity. The etiology of entropion varies by type, including involutional (age-related, due to lid laxity and weakening of supporting tissues), cicatricial (scarring from trauma, surgery, or inflammatory conditions like ), spastic (secondary to ocular irritation or inflammation), and congenital (present at birth from developmental abnormalities). Risk factors include advanced age, previous or injury, chronic dry eye, and infections such as in certain regions. Common symptoms include a sensation of a in the eye, redness, excessive tearing or dryness, light sensitivity, mucous discharge, and eyelid crusting, which can worsen with blinking or exposure to wind. If untreated, entropion may lead to complications such as corneal abrasions, ulcers, infections, or even vision loss from chronic epithelial damage. Diagnosis typically involves a comprehensive , including slit-lamp evaluation, lid distraction tests, and assessment of eyelid position to confirm inward rotation and rule out similar conditions like . Treatment options range from conservative measures—such as lubricating , taping the eyelid, or injections for temporary relief—to surgical interventions like Quickert sutures, tarsal strip procedures, or retractor reinsertion, which offer more permanent correction depending on the underlying cause and severity.

Background

Definition

Entropion is defined as the inversion or inward turning of the margin, most commonly affecting the lower , resulting in the lashes and skin rubbing against the and potentially leading to irritation or ulceration of the . This malposition disrupts the normal of the to the eye, causing the posterior to rotate inward toward the ocular surface. Anatomically, entropion involves instability in key structures that maintain eyelid position, including the tarsal plate—a dense fibrous framework providing rigidity—the orbicularis oculi muscle, which influences lid closure and tone, and the medial and lateral canthal tendons, which anchor the lid to the orbital rim for horizontal stability. Weakening or distortion of these components allows the eyelid margin to evert or invert abnormally. In contrast, ectropion represents the outward turning of the eyelid margin, exposing the and leading to different ocular surface issues. Entropion is broadly classified as congenital or acquired, with the latter encompassing involutional (age-related), cicatricial (scarring), and (muscle ) subtypes. The lower is far more commonly affected than the upper, though upper involvement can occur in specific forms like marginal entropion. Historically, cicatricial entropion was first described in ancient Indian texts, notably the around 600 BCE, which detailed surgical corrections for inversions causing lash irritation.

Epidemiology

Entropion is a significant malposition affecting older adults, with involutional entropion—the most common form—having a prevalence of approximately 2.1% in populations aged 60 years and older in Western countries. This age-related variant arises from progressive tissue degeneration and is more prevalent among females than males, attributed to factors such as thinner and greater eyelid laxity in women. The condition's incidence rises with advancing age, reaching up to 7.6% in individuals over 80 years. In contrast, cicatricial entropion, often resulting from chronic infections like , exhibits much higher prevalence in low-resource settings, particularly in and the , where remains endemic and can affect up to 15% of adults in hyperendemic communities through progressive scarring. accounts for the majority of infectious blindness globally, with approximately 1.9 million people visually impaired by its blinding sequelae, including entropion, as of 2024, predominantly in these regions. Congenital entropion, a rare subtype present at birth, occurs in fewer than 1 in 10,000 live births and is characterized by anomalous inversion due to structural defects. However, in Asian populations, related conditions like epiblepharon—typically affecting the lower and causing lash inversion that resembles entropion—affect approximately 10% of children, often resolving spontaneously but requiring in symptomatic cases. Globally, entropion rates for infectious causes have declined in developed nations due to and hygiene practices that have eradicated , while involutional forms remain stable. In developing regions, infectious entropion persists due to ongoing transmission, though progress continues: as of January 2025, 21 countries have eliminated as a problem. Post-2020, overall prevalence of involutional entropion has remained stable, but telemedicine has enhanced awareness and early detection in , with video consultations proving effective for assessing malpositions like entropion.

Pathophysiology

Causes

Entropion is classified into congenital and acquired forms based on its . Congenital entropion arises from developmental abnormalities such as dysgenesis of the lower eyelid retractors or an extra fold of skin on the that directs the lashes inward from birth. True congenital entropion is rare, but a related condition, epiblepharon—characterized by a horizontal skin fold and orbicularis muscle overriding the tarsus, causing lash misdirection—is common in East Asian children and can produce similar symptoms. These structural defects lead to instability and inward rotation of the margin, often exacerbated by facial paralysis in infants that allows unchecked retractor function. Acquired entropion encompasses several subtypes, each driven by distinct mechanisms. Cicatricial entropion results from scarring and of the posterior , causing tarsoconjunctival and shortening that pulls the margin inward; common triggers include inflammation from conditions like , chemical or thermal burns, trauma, Stevens-Johnson syndrome, or ocular cicatricial . Involutional entropion, the most prevalent form particularly among the elderly, stems from age-related tissue laxity, including horizontal laxity due to canthal tendon relaxation, tarsal atrophy, and orbital fat loss, combined with dehiscence or disinsertion of the lower retractors that destabilizes the lid margin. This allows the preseptal to override the pretarsal portion, further promoting inversion. Spastic entropion occurs due to sustained contraction of the in response to ocular surface irritation, inflammation, or infection, often following intraocular surgery, which exacerbates underlying laxity through preseptal muscle override. Mechanical entropion is induced by external forces, such as tumor masses or space-occupying lesions that exert pressure on the , distorting its alignment inward. Rare causes include iatrogenic factors, such as postoperative disinsertion of structures from prior surgeries like extraction or leading to cicatricial changes, and neurological conditions like that impair lid support.

Risk Factors

Entropion susceptibility is influenced by both non-modifiable and modifiable risk factors, which vary depending on the type of entropion, such as involutional, cicatricial, or congenital forms. Among non-modifiable factors, advanced age over 60 years significantly increases the risk, primarily due to age-related weakening of eyelid tissues and supporting structures in involutional entropion. East Asian ethnicity is associated with a higher prevalence of epiblepharon, a congenital condition causing lash inversion akin to entropion, with studies reporting rates exceeding 20% in Japanese children at age 1 year. A family history of congenital entropion also elevates risk, as evidenced by reports of autosomal dominant inheritance patterns in affected kindreds. Modifiable risk factors include chronic eye infections, such as exposure to in endemic regions, which can lead to cicatricial changes predisposing to entropion. Previous ocular , particularly , has been linked to a fourfold increased of lower involutional entropion compared to unoperated eyes. Autoimmune diseases like ocular cicatricial pemphigoid contribute to cicatricial entropion through progressive conjunctival scarring and eyelid distortion. Nutritional deficiencies, including in developing regions, can cause and spastic entropion with associated trichiasis. Environmental factors play a role, with poor in trachoma-endemic areas facilitating recurrent infections that heighten entropion risk. Prolonged sun exposure may accelerate periorbital skin aging and tissue laxity, indirectly contributing to involutional entropion development.

Clinical Presentation

Symptoms

Patients with entropion often experience a sensation in the affected eye, as if something is irritating the ocular surface, along with excessive tearing known as epiphora. These symptoms arise from the inward turning of the , causing eyelashes to rub against the and . Additional common complaints include , or sensitivity to light, and a burning sensation due to the ongoing lash-cornea contact. Patients may also report eye redness, itching, mucous discharge, dryness or dry eye sensation, and irritation that makes wearing lenses difficult or impossible. Symptoms typically begin as intermittent discomfort, particularly during or eye closure, but can progress to constant over time, especially in older individuals where muscle weakening exacerbates the condition. may develop if corneal exposure leads to surface damage. These effects are often more pronounced in dry environments or with exposure to wind, intensifying the sensation of and tearing. While these are subjective experiences, they are closely linked to observable eyelid inversion, though the focus here remains on patient-reported indicators.

Signs

The primary clinical sign of entropion is the inward rolling of the margin, most commonly affecting the lower , where the lashes and skin turn toward the eyeball, causing the eyelashes to contact the or . This malposition is often visible upon and can lead to mechanical of the ocular surface. On slit-lamp examination, secondary findings include conjunctival injection due to chronic friction, along with corneal abrasions manifesting as punctate or superficial epithelial defects that stain with fluorescein. In more advanced cases, filamentary may develop, characterized by strands adhering to the . Lower eyelid laxity is a key associated sign, assessed via the snap-back test, where the pulled lower lid returns slowly to the globe or not at all without blinking, indicating horizontal lid laxity. In cicatricial entropion, trichiasis is prominent, with misdirected lashes rubbing against the due to conjunctival scarring. Conversely, involutional entropion features horizontal laxity from age-related tissue weakening, often with override of the orbicularis muscle over the tarsus. Diagnostic maneuvers include gentle eversion of the to evaluate posterior tightness and retractor function, as well as of - by distracting the laterally from the (normal: less than 6 mm).

Diagnosis

History and Examination

The diagnosis of entropion begins with a detailed patient to determine the and guide further evaluation. Onset is typically inquired about to distinguish acute cases, such as entropion following irritation or surgery, from chronic forms like involutional entropion associated with aging or cicatricial entropion due to scarring from infections or trauma. Progression is assessed to note whether the condition is intermittent, as in early types, or worsening over time, often exacerbated by ongoing inflammation or lid laxity in elderly patients. Associated factors, including prior ocular trauma, infections (e.g., herpes zoster), inflammatory conditions, or surgical interventions, are elicited, as these can precipitate or cicatricial variants. Family is explored particularly for congenital entropion, which may involve genetic dysgenesis of lid structures, though it is rare in adults. Systemic symptoms are also reviewed to identify underlying causes, such as autoimmune disorders in cicatricial entropion, where patients may report associated conditions like Stevens-Johnson syndrome or ocular cicatricial pemphigoid. Common ocular complaints include redness, pain, , epiphora, and foreign body sensation, often linked to corneal exposure. In cases suggestive of systemic involvement, further workup for infections or autoimmune diseases may be indicated based on history alone. The physical examination starts with assessment of to detect any reduction due to corneal involvement, followed by external of the eyelids for inward turning of the margin, trichiasis, or signs of irritation such as lid edema or . evaluates for horizontal lid laxity using the distraction test, where excessive medial-lateral movement greater than 6 mm indicates tarsal instability, and the snapback test, where failure to return to position without blinking suggests poor tone. Basic motility tests assess lower lid in downgaze; reduced (less than 3-4 mm) points to retractor disinsertion, a key feature in involutional entropion. Red flags during history and examination include acute unilateral onset, which raises suspicion for spastic entropion secondary to irritation, and bilateral scarring or forniceal shortening, indicative of cicatricial causes like or . Standard protocols incorporate slit-lamp biomicroscopy for detailed lid margin evaluation and fluorescein to reveal corneal epithelial defects, abrasions, or resulting from lash-globe contact.

Diagnostic Tests

Slit-lamp biomicroscopy is a primary diagnostic for evaluating corneal involvement in entropion, allowing detailed visualization of epithelial defects, punctate , or ulceration caused by aberrant lash contact with the ocular surface. The (TBUT) test assesses tear film to identify evaporative dry eye secondary to entropion, with values under 10 seconds indicating that may exacerbate symptoms; this test is particularly relevant in cases where incomplete blinking or exposure contributes to ocular surface damage. Functional tests such as the lid distraction test quantify horizontal eyelid laxity by pulling the lower lid away from the ; a distance exceeding 6 mm is abnormal and supports a of involutional entropion due to tissue weakening. The snap-back test complements this by evaluating lid return after displacement, with delayed or incomplete snapping indicating laxity or retractor dysfunction. In suspected mechanical entropion, orbital imaging with or computed (CT) identifies underlying masses or tumors exerting traction on the lid, guiding further management. For cicatricial entropion linked to autoimmune conditions like ocular cicatricial pemphigoid, conjunctival biopsy with direct immunofluorescence is the gold standard, detecting linear IgG and deposits along the in 60-80% of cases to confirm the . Anterior segment (AS-OCT) has gained emphasis since 2020 for detecting subtle corneal epithelial irregularities and tear meniscus height alterations in entropion-associated dry eye, providing non-invasive quantitative assessment of surface changes.

Management

Nonsurgical Treatments

Nonsurgical treatments for entropion primarily aim to provide temporary relief from symptoms, particularly in cases of mild involutional or entropion, by addressing malposition and protecting the ocular surface without invasive procedures. These approaches are often indicated for acute entropion secondary to underlying ocular or as preoperative stabilization, with efficacy in symptom control ranging from temporary resolution in spastic cases to partial management in mild involutional presentations. Temporary measures include eyelid taping, which involves applying transparent medical to the lower to evert it away from the , thereby preventing lash-cornea contact; this method offers immediate but short-term relief, typically lasting until the tape is removed or displaced. type A (onabotulinumtoxinA) injections into the orbicularis oculi muscle are particularly effective for spastic entropion, relaxing the muscle to evert the lid; injections typically begin working within 3-5 days, achieve peak effect in 7-14 days, and provide relief for 3-6 months, with studies reporting resolution of entropion in nearly all treated spastic cases without systemic side effects. These interventions are ambulatory and suitable for patients unfit for or those requiring bridging . Lubrication therapies protect the from abrasion due to inverted lashes and maintain ocular surface integrity. Artificial tears and lubricating ointments are applied frequently to reduce friction and irritation, while moisture chambers—such as sealed or plastic shields—can be used to create a humid environment around the eye, minimizing evaporation and exposure in severe cases. Soft bandage contact lenses may also be prescribed to act as a protective barrier over the , alleviating discomfort in symptomatic patients. Medications address secondary complications, such as topical antibiotics (e.g., erythromycin ointment) for bacterial infections arising from corneal exposure or agents (e.g., steroid drops) for associated that exacerbates lid spasm. These are used adjunctively with other nonsurgical options to manage and prevent ulceration, particularly in acute presentations.

Surgical Treatments

Surgical treatments for entropion aim to restore normal eyelid anatomy by addressing the underlying structural defects, such as laxity, scarring, or congenital anomalies, through targeted operative techniques. These procedures are typically indicated after nonsurgical options fail or for persistent cases confirmed by preoperative evaluation. For involutional entropion, common in older adults due to age-related tissue weakening, procedures focus on correcting horizontal lid laxity and reattaching lower eyelid retractors. The Quickert-Rathbun involves placing everting sutures through the , tarsus, and to advance and tighten the retractors, often serving as a temporary or adjunct measure to induce formation for permanent correction. The Weis employs a transverse full-thickness blepharotomy followed by marginal sutures to create a barrier against orbicularis override and stabilize the lid margin, particularly effective for mild to moderate cases without significant laxity. For more pronounced laxity, the lateral tarsal strip technique is preferred, involving lateral canthotomy, tarsal stripping, shortening, and reattachment to the orbital rim to restore tension while preserving the canthal angle. Cicatricial entropion, resulting from conjunctival scarring due to conditions like or autoimmune diseases, requires techniques to release scar tissue and augment the posterior . Posterior lamella grafting, such as using hard palate mucosa, involves excising scarred tarsoconjunctival tissue and replacing it with a graft to lengthen and evert the lid margin, providing a stable, non-keratinized surface. Tarsal fracture, or modified tarsotomy, creates controlled breaks in the tarsus to allow rotation and eversion, often combined with grafts for severe cases to prevent recurrence. Congenital entropion, typically affecting the lower lid in infants or young children, is managed with procedures that shorten the lid horizontally and promote eversion. Horizontal lid shortening via tarsal resection or plication, combined with everting sutures, adheres the to the tarsus, correcting inversion and associated epiblepharon without excessive scarring. Postoperative care includes application of ophthalmic ointment twice daily to prevent , along with for lubrication; non-absorbable sutures are removed after approximately one week, while absorbable materials dissolve naturally. Overall success rates for these surgical interventions range from 85% to 95%, with low recurrence when addressed early and using combined techniques tailored to the .

Outcomes

Complications

Untreated or poorly managed entropion can lead to significant ocular complications due to chronic mechanical trauma from the inverted margin rubbing against the and . This persistent abrasion often results in corneal epithelial defects, progressing to , ulceration, or even perforation in severe cases. The damaged corneal surface becomes susceptible to secondary bacterial infections, which can escalate to more serious intraocular involvement such as if the infection spreads beyond the . Chronic sequelae of entropion include corneal scarring and opacity, which impair by causing irregular or central vision loss. Persistent irritation may also induce ongoing ocular pain and discomfort, while the visible malposition contributes to cosmetic , affecting patient . In cases of cicatricial entropion, the condition often stems from underlying autoimmune disorders such as ocular cicatricial pemphigoid, where progressive conjunctival scarring can worsen systemic disease manifestations if not addressed through appropriate medical management. Surgical interventions for entropion carry risks of rare adverse events, including overcorrection that results in , where the eyelid turns outward excessively. Recurrence is another potential issue, particularly in involutional entropion, with reported rates ranging from 5% to 10% depending on the technique and follow-up duration.

Prognosis

The prognosis for entropion is generally excellent with timely , achieving rates exceeding 90% in many surgical series. Early prevents progression to corneal damage, which can lead to irreversible vision impairment if the condition remains unaddressed. In contrast, delayed management increases the risk of poor outcomes due to secondary corneal complications. Key factors influencing include the underlying and timing of correction; early surgical intervention preserves more effectively by averting ocular surface damage. Recurrence rates vary by type, with cicatricial entropion showing higher relapse (approximately 18-20%) compared to involutional entropion (typically 1-5%). Postoperative monitoring is recommended for 6-12 months to assess and detect any recurrence early. Recent patient surveys indicate quality-of-life improvements in over 75% of cases following , primarily through relief of irritation and enhanced daily functioning. disparities affect outcomes, with better in regions with ready access to care; in endemic areas lacking , trachoma-related entropion results in significant loss, contributing to blindness in untreated individuals.

Entropion in Animals

In Dogs

Entropion is a common conformational in dogs, particularly affecting brachycephalic breeds with excess facial skin, such as the , where annual prevalence reaches 15.41% (95% CI 14.00–16.91), followed by the at 9.28% (95% CI 7.64–11.14), and English Bulldogs with rates exceeding 10%. This condition arises from inherited traits leading to inward rolling of the eyelids, often exacerbated by the anatomical features of these breeds. In , entropion typically presents as bilateral juvenile onset, manifesting before one year of age and causing irritation from eyelashes and lid margins rubbing against the , which frequently results in painful corneal ulcers affecting up to 14% of cases at initial presentation. Adult-onset forms are less common and usually secondary to scarring from prior ocular , infections, or chronic inflammation, leading to similar signs including epiphora, , and . For juvenile cases in puppies, temporary eyelid tacking with sutures is a standard initial intervention to evert the lids and allow growth, achieving resolution in 36.6% of eyes without further and a median treatment age of around six months. Definitive surgical correction involves techniques like the Hotz-Celsus procedure, which shortens the by excising a skin-muscle , or the Y-maneuver for more severe inversions, often combined with lateral wedge resection for optimal outcomes, yielding success rates of 94.2% to 98.4% per eye with breed-specific adjustments to account for skin laxity. Veterinarians recommend genetic screening through ophthalmic examinations like those certified by the Orthopedic Foundation for Animals (OFA) Eye Certification Registry to identify at-risk breeding stock, as programs have reduced entropion diagnosis risk by nearly twofold in cohorts post-implementation. Recent post-2022 studies emphasize emerging minimally invasive options, such as CO2 for mild cases, which precisely removes tissue to evert the lid with reduced scarring and faster recovery compared to traditional .

In Cats

Entropion in is a condition characterized by the inward rolling of the margin, leading to trichiasis where hair or eyelashes rub against the and . This results in ocular irritation and potential secondary complications such as corneal ulcers. Unlike in , where congenital entropion is more prevalent in certain breeds, it is less common in cats and often manifests as a secondary issue rather than a primary conformational defect.

Causes

Entropion in can be classified as primary or secondary. Primary entropion arises from developmental abnormalities in or orbital structure, most notably in breeds with brachycephalic (flat-faced) features such as or those with elongated facial anatomy like Maine Coons. Secondary entropion is more frequent and includes spastic forms triggered by ocular pain or from irritants like corneal ulcers, infections (e.g., herpesvirus-1), or ; cicatricial forms due to scarring from chronic inflammation or injury; and age-related cases in geriatric resulting from (sunken eye) and loss of orbital fat, with a mean age of onset around 11.3 years in over half of affected felines. Neurological issues or systemic dermatologic conditions can also contribute, though these are rarer.

Symptoms

Affected cats typically exhibit signs of ocular discomfort, including (squinting), epiphora (excessive tearing), (light sensitivity), and rubbing at the eyes with paws. Mucous or serous discharge is common, and in chronic cases, corneal exposure leads to ulceration, pigmentation, or sequestra formation. Brachycephalic cats may display subtler symptoms due to their facial conformation, but untreated entropion can progress to vision-threatening issues like corneal scarring or . In juvenile cats, symptoms often stem from ongoing rather than inherent .

Diagnosis

Diagnosis relies on a thorough ophthalmic by a , identifying eyelid inversion and trichiasis through direct visualization. Fluorescein staining detects corneal ulcers or abrasions, while a Schirmer tear test assesses tear production (normal range: 12-21 mm/min in ). Topical may be applied to evaluate the eyelid position without pain-induced . Underlying causes, such as infections or systemic diseases, require additional tests like viral screening for herpesvirus. Brachycephalic breeds warrant for conformational contributions.

Treatment

Initial management focuses on relieving irritation with topical antibiotics or lubricants to prevent secondary infections and corneal damage. For spastic entropion, temporary measures like eyelid tacking sutures or partial tarsorrhaphy (stitching eyelids together) allow resolution of underlying spasms, often lasting 10-14 days in young cats. Permanent correction involves surgery, preferably by a veterinary ophthalmologist, using techniques such as the modified Hotz-Celsus procedure (excision of a skin wedge to evert the lid) combined with lateral canthal closure, achieving success rates of 95-99%. In select cases, hyaluronic acid fillers offer a non-surgical option with approximately 92% efficacy, avoiding general anesthesia. Concurrent issues like ulcers must be addressed to prevent recurrence.

Prognosis and Complications

With prompt surgical intervention before significant corneal damage, the prognosis is excellent, restoring comfort and preserving in most cases. Prophylactic lateral canthal closure during reduces recurrence risk to near 0%, compared to 17% without it. Untreated or delayed cases risk chronic , corneal sequestra, or loss from scarring. Older cats with may require ongoing monitoring, but overall outcomes are favorable when managed early.

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