Congenital and acquired epiblepharon

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 by Gangadhara Sundar, MD on August 15, 2020.


Disease Entity

Congenital and acquired Epiblepharon

Disease

Epiblepharon is a developmental eyelid condition characterised by redundant anterior lamella presenting as an abnormal horizontal skin fold overriding the eyelid margin, resulting in misdirected lashes towards the conjunctiva and cornea. Typically seen in children and young adults of East Asian descent, it is much more common in the lower eyelids compared to the upper eyelids (Fig 1) [1]. Typically, it is seen as a congenital or developmental condition. However Acquired Epiblepharon may be seen in east Asian children and adults following orbital conditions like Thyroid Eye Disease, and other causes of proptosis. Other ethnic groups with some east Asian characteristics, like Hispanics, latin americans and Eskimos etc may also manifest this.

Etiology

While in East Asian children it is developmental and an exaggeration of normal anatomy, in other ethnic groups it is a true abnormality. Developmental epiblepharon results from poor or non-attachment of the lower and/or upper eyelid retractors to the overlying skin and subcutaneous tissues. This, along with the circumferential orbicularis oculi fibres, results in overriding of the preseptal over the pretarsal orbicularis causing a skin fold, which in turn results in an inward or posterior rotation of the eyelashes against the medial bulbar conjunctival and infero-medial and central cornea. When the eyelashes are long and thick with persistent conjunctival and corneal touch, they result in varying degrees of symptomatic kerato-conjunctivopathy. Long standing keratopathy may even result in irreversible corneal scarring. Other factors proposed include orbicularis hypertrophy and relatively poor attachment of the pretarsal orbicularis, athough disputed.

Secondary epiblepharon often arises from secondary increases in intraorbital pressure eg. Thyroid Eye Disease, orbital tumors (Fig 2)[2], acute orbital hemorrhage, obesity etc, in patients at risk with tight orbits and eyelids typical of East Asians.

Risk Factors

The well known and most common risk factor are children and young adults of East Asian descent, typically with parents who have either a weak or absent upper eyelid creases ('double eyelids'). Thus children with absent or poor eyelid creases and those with higher Body Mass Index (BMI) are at greater risk. While patients with soft finer lashes may be minimally symptomatic, those with thick stubby lashes are more symptomatic from resultant keratopathy. The tighter eyelids in East Asian orbits is also a risk factor.

Types of epiblepharon

Developmental, primary or congenital epiblepharon: This is the most common type typically seen in children and young adults of East Asian descent. Occasionally patients may present at a much later age having had symptoms for years but misdiagnosed as other conditions. In other ethnic groups, this is a transient developmental abnormality which usually resolves spontaneously.

Secondary, acquired epiblepharon: This is increasingly more recognized in patients at risk with secondary underlying orbital pathology with resultant proptosis and tight eyelids and may be seen at any age.

Severity and Grading

Khwarg et al have proposed a practical classification based on the degree and extent of eyelid skin fold, lash-corneal touch and keratopathy.

Primary prevention

None.

Diagnosis

The diagnosis of epiblepharon is primary clinical, based on history, clinical suspicion and dynamic slit lamp exam of the eye with and without corneal staining.

History

The classic history and presentation is a young child of East Asian descent, who presents with rubbing, frequent blinking, tearing and/or discharge from one or both eyes, where other conditions like nasolacrimal duct obstruction and allergic conjunctivitis have been ruled out. Most children may have received a course of topical antibiotics or antiallergics without much response. Occasionally, younger and older adults may have had similar symptoms since childhood or even present with having had repeated epilations or trimmed eyelashes.

Patients with an acquired epiblepharon often present with typical clinical features of an underlying orbital disease i.e., thyroid eye disease, orbital tumor or inflammatory disease, orbital haemorrhage.

Physical examination

A high degree of suspicion is often necessary to make a diagnosis. External examination may reveal a narrow palpebral fissure, weak or absent upper eyelid crease, any of the variants of medial epicanthal fold and occasionally wet sticky eyes. The eyelid margin and the posterior lamella are in their normal position. Slit lamp exam often shows a variable degree of the eyelid skin overriding the lower eyelid margin. The lashes are directed against the medial bulbar conjunctiva and infero-medial cornea, especially in down gaze and adduction. Fluorescein staining of the cornea and conjunctiva is usually positive varying from fine superficial punctate keratopathy to confluent coarse keratopathy. Rarely, in older children and adults with long standing duration, corneal scarring may be present as well.

Upper epiblepharon manifests as misdirected medial eyelashes with intermittent corneal-conjunctival touch especially in upward and inward gazes. The typical eyelid skin fold is not seen with upper epiblepharon unless in severe cases.

Symptoms

In early stages and very young children, this is often asymptomatic. Common symptoms include Irritation, foreign body sensation, frequent blinking or rubbing of eyesitching, Tearing with/without discharge

Signs

The most common signs of Epiblepharon include: ¥ variable lower eyelid skin fold, more prominent medially ¥ Eyelid margin and posterior lamella are in normal position ¥ Lash corneal-conjunctival touch, especially in downgaze and adduction in lower epiblepharon and up gaze in upper epiblepharon. ¥ Fine, intermediate to coarse and confluent keratopathy that stains with fluorescein. (Fig 3a) [3], (Fig 3b) [4].

Abnormal eyelashes may be bent or broken. Occasional stumps from clipped lashes may be seen (Fig 4) [5]. Cornea scarring in severe and long standing keratopathy.

Upper epiblepharon typically manifests with a weak or absent eyelid crease with downward rotation of the eyelashes with lash-corneal touch in primary or up gaze.

Thus these symptoms are mistaken for chronic and allergic conjunctivitis, congenital nasolacrimal duct obstruction in very young children.

Clinical diagnosis

The diagnosis of Epiblepharon is clinical. It may be easily missed in early and mild disease in very young children especially when not looked for. In a symptomatic child, the presence of eyelashes against the cornea and conjunctival in any gaze is diagnostic of this disease. Associated keratopathy determines the threshold for medical and when indicated surgical intervention.

Diagnostic procedures

Epiblepharon is primarily a clinical diagnosis. The main diagnostic procedure is fluorescein staining with documentation by slit lamp photography regarding the nature of severity of keratopathy.

Laboratory test

None

Differential diagnosis

The differential diagnosis for Epiblepharon and their differentiating features are as follows:

  • Trichiasis is an acquired condition resulting from a malpositioned eyelash misdirected against the globe.
  • Distichiasis is a developmental condition with an aberrant additional row of eyelashes arising from Meibomian gland orifices.
  • Entropion of lower eyelid: True inward rotation of posterior lamella and lid margin.
  • Nasolacrimal duct obstruction: symptoms since birth, more commonly unilateral, tearing and discharge.
  • Allergic conjunctivitis: stringy mucus discharge, conjunctival injection, papillary conjunctival changes.

Natural history

Most children are asymptomatic as the eyelashes are fine and may not induce keratopathy even with lash-corneal touch. As the lashes get thicker and longer and with increasing skin fold, especially in those with higher body mass index. Keratopathy may evolve from asymptomatic fine punctate erosions to confluent keratopathy, and even corneal scarring. A higher astigmatism rate has also been reported.


Management

Developmental epiblepharon: Most children may be managed conservatively with lubricants and regular follow up until resolution. Indications for surgical intervention include persistent symptoms and significant keratopathy despite conservative management.

Minimally invasive procedures include tissue filler injection into the valley of the skin fold or everting sutures result in transient improvement albeit with higher recurrence rates.

Surgical management is often indicated when symptoms and signs are persistent and severe. Although both transconjunctival and transcutaneous procedures have been described, the latter is most commonly performed and reportedly most successful. The most commonly recommended procedures is the modified Hotz procedure, which involves excision of an ellipse of redundant skin mostly medially, with sutures placed to ensure outward rotation of the eyelashes with wound closure.

Acquired epiblepharon: While most acquired epiblepharon may resolve with resolution or treatment of the underlying primary orbital pathology eg. Orbital tumors, hematoma, etc, occasionally an orbital decompression may be indicated as in moderate to severe thyroid eye disease.

Outcomes and complications

Success rates are over 95% with high satisfaction rates. Potential complications include undercorrections, especially medially, overcorrections resulting in transient ectropion and visible lid scar, all of which can be prevented with a good technique.

Prognosis

The prognosis is generally excellent in patients who have minimal intermittent lash-corneal touch with fine lashes and those who receive adequate and timely surgical correction. Revision and repeat surgeries are rarely indicated.


References

  1. Kim JS, Jin SW, Hur MC, et al. The clinical charateristics and surgical outcomes of epiblepharon in Korean children: a 9-year experience. J Ophthalmol 2014; 156-601.
  2. Sundar G, Young SM, Tara S, et al. Epiblepharon in East Asian patients: the Singapore experience. Ophthalmology 2010; 117(1): 184-9.
  3. Chang EL, Hayes J, Hatton M, et al. Acquired lower epiblepharon in patients with thyroid eye disease. Ophthal Plast Reconstr Surg 2005; 21: 192-6.
  4. Khwarg SI, Lee YJ. Epiblepharon of the lower eyelid: classification and association with astigmatism. Korean J Ophthalmol 1997; 1:111-7.
  5. Naik MN, Ali MJ, Das S, et al. Nonsurgical management of epiblepharon using hyaluronic acid gel. Ophthal Plast Reconstr Surg 2010; 26(3): 215-7.
  6. Revere KE, Foster JA, Katowitz WR, Katowitz JA. Developmental Eyellid Abnormalities in Pediatric Oculoplastic Surgery 2nd Ed. Ed Katowitz JA, Katowitz WR. Springer 2018. ISBN 978-3-319-60812-9.