39. Blepharoptosis



10.1055/b-0038-163163

39. Blepharoptosis

Jason E. Leedy, Jordan P. Farkas

Definition


Blepharoptosis is drooping of the upper lid margin to a position that is lower than normal. (Normal upper lid position is at the level of the upper limbus.)



Anatomy


1


(fig. 39-1)

Fig. 39-1 Differences between normal and ptotic upper eyelid anatomy.


Levator Aponeurosis




  • Origin: Lesser wing of the sphenoid



  • Insertion: Orbicularis oculi, dermis, tarsus



  • Innervation: Superior division of oculomotor nerve (CN III)



  • Action: Provides 10-12 mm of eyelid elevation



  • Embryology: Develops in the third gestational month from the superior rectus muscle



  • Anterior lamella of the levator muscle forms aponeurosis



  • Posterior lamella of the levator muscle forms Müller muscle



  • Approximately 2-5 mm above the tarsus the anterior portion of the levator aponeurosis joins the orbital septum.



Müller Muscle




  • Origin: Posterior lamella of levator muscle



  • Insertion: Superior border of tarsus



  • Innervation: Sympathetics



  • Action: Provides 2-3 mm of eyelid elevation



Frontalis Muscle




  • Origin: Galeal aponeurosis



  • Insertion: Suprabrow dermis



  • Innervation: Frontal branch of facial nerve



  • Action: Elevates brow and upper eyelid skin



Etiologic Factors/Pathophysiology


2 , 3



True Ptosis




  • Intrinsic drooping of the affected eyelid



Pseudoptosis: Conditions That Mimic True Ptosis




  • Grave disease: Retraction of contralateral lid can give appearance of ptosis on unaffected side



  • Hypotropia: Downward rotation of the globe with accompanying lid movement



  • Duane syndrome: Extraocular muscular fibrosis and globe retraction



  • Posttraumatic enophthalmos



  • Contralateral exophthalmos: Gives impression of ptosis on the unaffected side



  • Chronic squinting from irritation



Congenital Ptosis


2 , 3




  • Developmental dysgenesis in the levator muscle



  • Idiopathic persistent ptosis noticed shortly after birth



  • Usually not progressive



  • Signs confined to the affected eyelid(s)



  • Decreased palpebral aperture with reduction of the pupil reflex to upper eyelid margin measurement (marginal reflex distance test [MRDI])



  • Decreased levator excursion




    • Poor or absent levator function reflected in the absence of the supratarsal crease



  • Ptotic eyelid generally higher than the normal eyelid during downgaze



  • Inheritance pattern unclear



  • Levator biopsies in congenital ptosis show absence of striated muscle fibers with fibrosis.



Tip:


History alone usually can distinguish congenital from acquired ptosis, but if there is a question, lagophthalmos on downward gaze is characteristic of congenital ptosis, because levator fibrosis prevents downward lid migration.




  • Associated ocular abnormalities




    • Coexistent strabismus and amblyopia




      • Caused by pupil occlusion



    • Marcus Gunn jaw-winking syndrome




      • Synkinesis of upper lid with chewing



      • Seen in 2%-6% of congenital ptosis



      • Caused by aberrant innervation from fifth cranial nerve



    • Blepharophimosis syndrome




      • Triad of ptosis, telecanthus, and phimosis of lid fissure



    • Congenital anophthalmos or microphthalmos




      • Hypoplasia of the lids, globe, and orbital bones



    • Coexistent eyelid hamartoma




      • Neurofibromas



      • Hemangiomas



      • Lymphangiomas



Acquired Ptosis


2 , 3




  • Myogenic




    • Involutional myopathic (senile ptosis)




      • Most common type



      • Stretching of the levator aponeurosis attachments to the anterior tarsus



      • Dermal attachments are maintained and therefore the supratarsal crease rises.



      • Levator function is usually good.



    • Chronic progressive external ophthalmoplegia




      • Progressive muscular dystrophy affects the extraocular muscles and levator.



      • 5% of cases involve the facial and oropharyngeal muscles.



  • Traumatic




    • Second most common type



    • Allow recovery of myoneural dysfunction, resolution of edema, and softening of scar (approximately 6 months).



    • This can occur after cataract surgery from dehiscence of levator aponeurosis.



  • Neurogenic




    • Third nerve palsy: Paralyzes levator muscle



    • Horner syndrome: Paralyzes Müller muscle



    • Myasthenia gravis




      • Primarily, young women and old men are affected.



      • Ptosis worsens with fatigue, at the end of the day.



      • Improvement with neostigmine or edrophonium is characteristic.



  • Mechanical




    • Upper lid tumors



    • Severe dermatochalasis (excessive upper lid skin), brow ptosis



Evaluation


2 , 3



Determination of Cause




  • Congenital or acquired



Tip:


Evaluate for lagophthalmos during downward gaze. This indicates levator fibrosis, which is more commonly seen with congenital cases.



Degree of Ptosis


(table 39-1)




  • Always compare with contralateral side.



  • Measure amount of descent over upper limbus.




    • 1-2 mm: Mild



    • 3 mm: Moderate



    • 4 mm or more: Severe



  • Record palpebral fissure height.




















Table 39-1 Degree of Ptosis

Degree of Ptosis


Mild


Moderate


Severe


Lid descent over upper limbus


1-2 mm


3 mm


>4 mm



Levator Function


(Table 39-2)




  • Measure from extreme downward gaze to extreme upward gaze while immobilizing the brow.



  • >10 mm: Good



  • 5-10 mm: Fair



  • <5 mm: Poor




















Table 39-2 Levator Function

Levator Function


Good


Fair


Poor


Levator excursion


>10 mm


5-10 mm


0-5 mm

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May 18, 2020 | Posted by in Aesthetic plastic surgery | Comments Off on 39. Blepharoptosis

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