16 articles
Abscess of eyelid
Abscess of eyelid (ICD-11 9A01.1), a pus collection in eyelid tissue, usually staphylococcal; includes hordeolum and abscess complicating preseptal cellulitis, treated by incision and drainage plus antibiotics.
Allergic contact blepharoconjunctivitis
Allergic contact blepharoconjunctivitis, also called contact blepharoconjunctivitis, is a delayed hypersensitivity reaction of the eyelid skin and conjunctiva, typically triggered by cosmetics, metals, or eye drops.
Atopic keratoconjunctivitis
Atopic keratoconjunctivitis, first described by Hogan in 1953, is a chronic bilateral inflammation of the conjunctiva and cornea in people with atopic dermatitis, and can threaten vision.
Blepharophimosis-ptosis-epicanthus inversus syndrome
BPES (blepharophimosis-ptosis-epicanthus inversus syndrome), also called blepharophimosis syndrome, is a rare autosomal dominant FOXL2-related eyelid malformation with ptosis, telecanthus, and sometimes primary ovarian insufficiency.
Chlamydial conjunctivitis
Chlamydial conjunctivitis, or adult inclusion conjunctivitis, is a chronic follicular conjunctivitis caused by sexually transmitted Chlamydia trachomatis serovars D-K; related neonatal and trachoma forms exist, treated with systemic azithromycin or doxycycline.
Congenital eyelid retraction
Congenital eyelid retraction, classified as ICD-11 LA14.05, is a rare kinetic eyelid anomaly present at birth where one eyelid sits too high or too low.
Congenital ptosis
Congenital ptosis, also called congenital blepharoptosis, is upper eyelid drooping present at birth, usually from dystrophic levator palpebrae superioris muscle. Unilateral in about 75% of isolated cases; graded by MRD1; treated with levator resection or frontalis sling; risk includes amblyopia.
Hordeolum internum
Hordeolum internum (internal hordeolum, internal stye): acute bacterial infection, usually Staphylococcus aureus, of a meibomian gland inside the eyelid; deeper and more diffuse than an external stye, treated with warm compresses, resolving in 1–2 weeks.
Infectious blepharitis
Infectious blepharitis, ICD-11 9A01.3 (感染性眼瞼炎), is bacterial infection of the eyelid margin causing itching, tearing, and lash crusting; spread by contact, endogenous spread, or fomites, and treated with lid hygiene plus antibiotics.
Marcus-Gunn syndrome
Marcus-Gunn syndrome, or Marcus Gunn jaw-winking syndrome (MGJWS), is a congenital ptosis with trigemino-oculomotor synkinesis: the drooping upper eyelid elevates during jaw movements, occurring in roughly 2-13% of congenital ptosis cases.
Papillary conjunctivitis
Papillary conjunctivitis: conjunctival inflammation with vascular papillae on the tarsal conjunctiva, mainly allergic, drug-induced, or mechanical; giant papillary conjunctivitis (GPC) is the contact lens form, first described by Spring in 1974.
Paralytic lagophthalmos
Paralytic lagophthalmos is incomplete eyelid closure from facial nerve (CN VII) paralysis, mainly Bell's palsy, also leprosy, trauma, or tumors; it risks exposure keratopathy and is treated with lubricants, tarsorrhaphy, or eyelid weight implants.
Serous conjunctivitis, except viral
Serous conjunctivitis, except viral (ICD-10-CM H10.23; ICD-11 9A60.6) is a diagnostic classification for acute conjunctivitis with clear, watery discharge not attributed to a virus, coded by laterality subcodes H10.231-H10.239.
Tarsal kink syndrome
Tarsal kink syndrome (ORPHA:99170), a rare congenital eyelid disorder: a horizontal kink in the upper tarsal plate causing upper lid entropion, blepharospasm, absent eyelid crease, and risk of corneal ulceration, treated surgically.
Telecanthus
Telecanthus, also called dystopia canthorum or pseudohypertelorism, is an increased distance between the inner eyelid corners (medial canthi) with normal pupil spacing, usually from genetic syndromes or facial trauma, treated surgically.
Vascular abnormalities of conjunctiva
Vascular abnormalities of conjunctiva (ICD-11 9A61.40, ICD-10 H11.41): abnormalities of conjunctival blood vessels, including telangiectasia, lymphangiectasia, malformations, and vascular tumors, often signaling systemic disease.