Ankyloblepharon

Patients may have symptoms such as

• Complete, partial, or interrupted fusion of upper and lower eyelids.
• Horizontal foreshortening of the palpebral fissure.
• Pseudoexotropia due to lateral ankyloblepharon.
• Pseudoesotropia due to medial ankyloblepharon.
• Reduced eyelid excursion.
• Associated features such as anophthalmos (absence of eyeball), microphthalmos (small eyeball), ptosis (drooping of eyelid), or cleft lip.
• Downward displacement of lateral canthal angle.
• Large fluid cyst due to accumulation of lacrimal tears in cases of total ankyloblepharon.

Congenital ankyloblepharon:

There is epithelial fusion of the eyelid margins of the developing foetus at about 9^th week of gestation. Complete separation usually does not occur until about 7^th month of foetal life. Rarely, the lid margins may remain fused at birth, which results in ankyloblepharon. The exact mechanism is still not clear. The problem may be in the epithelium fusion stage, in which there is fusion of the mesoderm of the lid margin rather than purely the epithelium.

Ankyloblepharon may be an isolated sporadic malformation. It may also be associated with other malformations which are presumably inherited as an autosomal dominant condition in some cases and as an autosomal recessive condition in others.

Congenital ankyloblepharon may be associated with central nervous system and/or cardiac anomalies, cleft lip and/or palate and gastrointestinal abnormalities.

• Hay-Wells syndrome: A rare autosomal dominant disorder, known as Hay-Wells syndrome, may be associated with ankyloblepharon, ectodermal defects, and cleft lip and palate (AEC syndrome).
• Curly hair, ankyloblepharon and nail dysplasia (CHAND) syndrome: This is an autosomal recessive disorder which is characterised by ankyloblepharon and ectodermal dysplasia, but affected patients have curly hair and hypoplastic nails, with absence of cleft lip or palate.
• Edwards’ syndrome or Trisomy 18: Edwards’ syndrome or Trisomy 18 patients may also have ankyloblepharon filiforme adnatum.
• Rapp-Hodgkin syndrome: This is an autosomal dominant syndrome characterised by ectodermal dysplasia, cleft lip and/or palate, and mid-facial hypoplasia.

Acquired ankyloblepharon:

Various aetiologies for acquired ankyloblepharon have been described.

• Chemical injuries to the eyes.
• Burns.
• Stevens-Johnson syndrome.
• Post traumatic prolonged contact of upper and lower eyelid.
• Trachoma.
• Ulcerative blepharitis.
• Herpes simplex blepharoconjunctivitis.
• Diphtheritic conjunctivitis. 

Diagnosis of ankyloblepharon is based on clinical features.

Congenital ankyloblepharon

The eyelid margins are usually fused laterally, and less commonly medially. This condition may be associated with other developmental anomalies such as ptosis, microphthalmos, anophthalmos, or cleft lip. Lateral canthal angle may be displaced downward giving an anti-mongoloid appearance to the palpebral fissure. Lateral canthal tendon is lax or not developed so that there is significant laxity of the lower eyelids.

In ankyloblepharon filiforme adnatum, one or more narrow epithelial strands connect the central part of lower and upper eyelid margins. These vary in dimensions from 0.5 mm to 5 mm in width, and may range from 1 mm to 10 mm in length. The zone of attachment lies between the meibomian gland orifices and the eyelashes.

In total ankyloblepharon, lacrimal secretions may accumulate beneath the eyelids forming a fluid cyst.

Acquired ankyloblepharon

Commonly, acquired ankyloblepharon is due to progressive conjunctival scarring resulting in fusion of the eyelids. Patients usually have a history of progressive scarring related to the primary disease. The eyelids show fusion from scar tissue.

Investigations

Detailed ocular examination is performed including measurement of intraocular pressure. Any ocular features of hydrocephalus are noted. 

Screening may be required to rule out any genetic disorder associated with ankyloblepharon.

Differential diagnosis

Ankyloblepharon may be differentiated from

• Blepharophimosis: In blepharophimosis, the palpebral aperture is reduced and there is telecanthus (increased medial intercanthus distance), but the eyelid margins are normal.
• Euryblepharon: In both euryblepharon and ankyloblepharon, the lateral portion of the eyelid may be lax and displaced downward. In ankyloblepharon, the eyelid margins are fused together for some distance producing a shorter horizontal palpebral fissure.  The fissure is longer than normal in cases ofeuryblepharon.
• Cryptophthalmos (congenital absence of eyelid with skin passing continuously from head to cheeks over mal-formed eye).
• Microphthalmos (small eyeball).
• Pseudostrabismus

Management should be carried out under medical supervision.

Indications for therapy in cases of congenital and acquired cases of ankyloblepharon are similar. Presence of a significant central ankyloblepharon may occlude vision. In congenital type, it may potentially cause an occlusion type amblyopia. A significant nasal or temporal ankyloblepharon may restrict peripheral vision. Normal opening and closing of eyes may also be affected.

Management of ankyloblepharon is surgical and is indicated for improvement of visual field or for cosmetic reasons.

Surgical therapy

A potential contraindication to ankyloblepharon surgery is the problem of corneal exposure following release of marginal adhesions. This is significant in cases of ankyloblepharon developing after trauma, since other injuries such as damage to fifth and seventh intracranial nerve may be present. This is also true in similar cases with injury to cornea, lacrimal gland, decreased corneal sensitivity, decreased tear production, or lagophthalmos.  Surgical procedures include

Congenital ankyloblepharon

Therapeutic approach to congenital ankyloblepharon depends upon the type and extent of lid margin adhesions. Spontaneous resolution of very fine filaments may occur in some cases of ankyloblepharon filiforme adnatum (AFA).

• Breaking of ankyloblepharon filiforme adnatum (AFA) bands: Fine bands may be broken with muscle hook or by forcible separation of the eyelids. The remnants of bands usually shrink on their own and resolve.
• Bipolar cautery: Some fine filaments resist easy breakage under stretch. Bipolar cautery may be applied to the bases of fine filaments to break them.
• Separation of ankyloblepharon with reconstruction of eyelid margin: More severe cases require separation of ankyloblepharon with reconstruction of eyelid margin. Young children require general anaesthesia for the procedure.

Acquired ankyloblepharon

Determine the cause of scarring in cases of acquired ankyloblepharon. Any associated inflammation must be treated first before resorting to any surgical therapy.

• Acquired ankyloblepharon with symblepharon: Acquired ankyloblepharon due to trauma or inflammatory conditions is frequently associated with formation of symblepharon (adhesion between eyeball and the eyelid). Ankyloblepharon repair may be combined with release of symblepharon adhesion and covering with mucous membrane or amniotic membrane graft.
• Acquired ankyloblepharon without symblepharon: In mild cases of acquired ankyloblepharon without symblepharon, separation with blunt scissors may suffice. Irregularities at the eyelid margin may be thinned and trimmed and the raw surface is covered.

Prognosis

Visual prognosis is usually good if separation of eyelids is performed in timely manner.

Cosmetic appearance of the eyelids after separation of bands is usually very good in congenital ankyloblepharon.

The process of scarring may hamper the healing process following eyelid and corneal reconstructive surgery in cases of acquired ankyloblepharon.