Classification and management of eyelid disorders Flashcards
1
Q
Congenital anomalies of eyeid occur when?
A
Most congenital abnormalities of eyelids occur during second month of gestation because of failure of fusion or an arrest of development.
2
Q
Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome
A
- Autosomal Dominant
- Blepharophimosis (horizontally narrow and vertically narrow palpebral fissure), + telecanthus (increased distance between medial canthi) + severe ptosis + epicanthus inversus (eyelid fold prominent in lower eyelid)
- FOXL2 gene, Chromosome 3
- Type I = early loss of ovarian function in women, Type II
- Additional findings = lateral lower eyelid ectropion 2/2 vertical eyelid deficiency, poorly developed nasal bridge, hypoplasia of superior orbital rim, ear deformities, hypertelorism
- Repair of ptosis usually requires frontalis suspension for adequate lift
7.
3
Q
Congenital Ectropion
A
- Associated with BPES, Down syndrome, icthyosis
- 2/2 vertical insufficency of anterior lamella of eyelid
- Chronic epiphora, exposure K
- Mild = no treatment
- Severe/symptomatic = Lateral canthal tendon tightening and vertical lengthening of anterior lamella with full-thickness skin graft
4
Q
Euryblepharon
A
- Vertical shortening and horizontal lengthening of eyelid
- Associated with BPS
5
Q
Ankyloblepharon
A
- Eyelids fuse 8-20w gestation
- Partial or complete fusion of eyelids by webs of skin
- Can usually be opened by scissors
6
Q
Epicanthus
A
- Medial canthal fold that may result from immature midfacial bones or a fold of skin and subcutaneous tissue
- May cause pseudoesotropia because of decrease scleral show
- Epicanthus tarsalis = can be normal variation in Asian eyelid
- Most become less apparent with normal growth of facial bones
- Epicanthus inversus rarely resolves with facial growth
- Respond to linear revisions = Z-plasty and Y-V plasty
7
Q
Epicanthus
A
8
Q
Epiblepharon
A
- Lower eyelid pretarsal muscle and skin ride above lower eyelid margin causing cilia to assume a vertical position. Eyelid margin in normal position
- Most common in Asian children
- Cilia touch K in downgaze
- May NOT require surgery as tends to diminish with maturation of facial bones
- May result in acute or chronic K epithelial irritation in which case excess skin and muscle fold excised
9
Q
Congenital Entropion
A
- Due to lower eyelid retractor dysgenesis, structural defects in tarsal plate, relative shortening of posterior lamella
- Unlikely to improve and may need surgery
- Repaired with removal of skin + orbicularis muscle + advancement of lower eyelid retractors to tarsus
- Tarsal kink = form of congenital entropion where tarsal plate of upper eyelid folding causing entropion
10
Q
Epicanthus
A
11
Q
Epiblepharon
A
12
Q
Congenital distichiasis
A
- Extra row of eyelashes in orifices of MG
- Congenital = embryonic pilosebaceous units improperly differentiate into hair follicles
- Treatment if symptomatic or keratopathy develops
- Lubricants and CL may be sufficient
- May need electrolysis, cryoepilation
13
Q
Congenital coloboma
A
- True coloboma includes defect in eyelid margin and eyelid
- When in lower eyelid = associated with Goldenhar syndrome and lacrimal deformities
14
Q
Crytophthalmos
A
- Presents with partial or complete abscence of eyebrow, palpebral fissure, eyelashes, conjunctiva
- Partially developed adnexa fused to anterior segment of globe
- Histologically = levator, orbicularis muscle, tarsus, conjunctiva and MG attenuated or absent
15
Q
Infantile Hemangioma
A
- Aka capillary hemangioma
- Usually appear over first weeks or months of life
- Associated with amblyopia
- Treatment recommended for those with occlusion of visual axis or disfigurement
- Increases in size until 1 yo and decreases over next 3-7 years
- Vision threatened and lesion limited to eyelid = topical timolol gel or intralesional steroid. More widespread involvement addressed with systemic propranolol or oral steroids
- Non-responders to b blockers or cannot take b blockers = intralesional steroids considered BUT risk of eyelid necrosis, embolic retinal vascular occlusion, systemic adrenal suppression
- Topical clobetasol proprionate and interferon a have been tried