Clinical Conditions of the Eyelids and Lashes

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Vocabulary flashcards covering clinical definitions, etiology, presentation, and complications of disorders affecting the eyelashes and eyelids.

Last updated 3:45 PM on 9/15/26
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62 Terms

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Eyelash ptosis

Misdirection of the superior eyelashes where they point downward, caused by laxity of eyelid structures such as the orbicularis oculi or tarsal plate.

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Trichomegaly

Excessively long, thick, or deeply pigmented eyelashes, defined as lashes exceeding 12mm12\,mm in length.

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Madarosis

Loss or thinning of eyelashes resulting from hair follicle scarring (seen with malignant eyelid tumors) or non-scarring conditions (such as atopic dermatitis).

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Poliosis

Whitening or depigmentation of the eyelashes or eyebrows caused by destruction of melanocytes at the base of the hair follicle.

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Trichiasis

An acquired abnormality where normally positioned eyelashes are misdirected backwards toward the globe.

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Distichiasis

An extra row of eyelashes emerging from the orifices of the meibomian glands, occurring when sebaceous glands become pilosebaceous units.

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Anterior blepharitis

Inflammation of the eyelid margin anterior to the meibomian glands, presenting as staphylococcal (with collarettes at the lash base) or seborrheic (with greasy lid margins and matted lashes).

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Angular blepharitis

Eczematoid inflammation localized to the lateral or medial canthus, caused by Staphylococcus aureus (dry, scaly skin) or Moraxella lacunata (wet, macerated skin with white frothy discharge).

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Posterior blepharitis

Inflammation of the meibomian glands and posterior lid margin characterized by meibomian gland capping, thickened meibum expression, lid hyperemia, and an oily/frothy tear film.

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Phthiriasis palpebrarum

Parasitic infection of the eyelashes caused by pubic lice (Pediculosis pubis), characterized by lice anchored to the lashes and small brownish opalescent nits.

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Demodex folliculorum

Parasitic mite infection residing in eyelash hair follicles that presents with cylindrical dandruff at the base of short, thin lashes.

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Demodex brevis

Parasitic mite infection residing deep within the meibomian glands, presenting with meibomian gland capping and posterior lid inflammation.

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External hordeolum

Acute localized bacterial infection of a Gland of Zeis or Gland of Moll along the eyelid margin, presenting as a painful, hyperemic pustule.

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Internal hordeolum

Acute localized bacterial infection of a meibomian gland, presenting with localized pain, heat, and swelling within the tarsal plate without an external pustule on the lid margin.

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Preseptal cellulitis

Bacterial infection of the subcutaneous tissue anterior to the orbital septum, presenting with eyelid swelling, redness, warmth, and pain without affecting extraocular movements or vision.

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Orbital cellulitis

Life-threatening bacterial infection of the soft tissues posterior to the orbital septum, characterized by proptosis, pain with eye movements, double vision, and potential vision loss.

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Blepharochalasis

Rare condition characterized by recurrent, painless, non-pitting edema episodes of the eyelids, leading to thin, wrinkled, redundant skin and secondary ptosis.

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Allergic edema

Bilateral periorbital eyelid swelling caused by an acute inflammatory hypersensitivity reaction to allergens, presenting with severe itching and conjunctival chemosis.

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Contact dermatitis

Inflammatory skin condition triggered by direct exposure to topically applied irritants or allergens, presenting with eyelid hyperemia, severe itching, scaling, and chemosis.

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Atopic dermatitis

Chronic inflammatory skin condition associated with asthma and hay fever, presenting with thickened, crusty, hyperemic eyelid skin and madarosis.

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Herpes simplex eyelid dermatitis

Localized HSV-1 viral infection presenting with a prodromal tingling sensation followed by grouped periorbital vesicles and swelling that respects the facial midline.

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Herpes Zoster Ophthalmicus

Reactivation of the Varicella Zoster Virus along the ophthalmic branch of the trigeminal nerve (V1V_1), presenting with a painful maculopapular rash respecting the facial midline.

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Chalazion

Chronic, painless, sterile lipogranulomatous inflammatory lesion of a meibomian gland caused by obstructed lipid breakdown products leaking into eyelid tissue.

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Sebaceous cell carcinoma

Aggressive malignancy of the sebaceous glands that often mimics a chronic or recurrent chalazion and causes lid margin thickening and madarosis.

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Cutaneous horn

Hyperkeratotic, conical protrusion emerging from the skin or eyelid margin, arising from underlying benign, precancerous, or malignant lesions.

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Pyogenic granuloma

Benign vascular growth of blood vessels triggered by trauma or surgery, presenting as a painful, bright red or purple polypoidal lesion that bleeds easily.

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Keratoacanthoma

Fast-growing hair follicle tumor presenting as a dome-shaped nodule with a central keratin-filled crater, capable of transforming into Squamous Cell Carcinoma.

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Moll cyst

Small, painless, translucent retention cyst arising from the apocrine sweat glands located along the anterior eyelid margin.

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Zeis cyst

Small, painless, opaque white or yellow retention cyst arising from sebaceous Glands of Zeis on the anterior lid margin.

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Milia

Tiny, white, round papules arising from pilosebaceous units occurring in clusters on the eyelid skin.

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Eccrine hidrocystoma

Translucent retention cyst arising from eccrine sweat glands located on the eyelid skin away from the lid margin.

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Squamous cell papilloma

Common benign skin tag composed of hyperplastic squamous epithelium with a vascular core, presenting as a soft, pedunculated or sessile lesion.

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Verruca vulgaris

Benign viral eyelid wart caused by Human Papillomavirus (HPV), presenting as a skin-colored, waxy, or finger-like projection on the lid margin.

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Molluscum contagiosum

Viral skin infection caused by a poxvirus, presenting as smooth, pale, waxy, umbilicated nodules along the eyelid margin.

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Xanthelasma

Subcutaneous yellow lipid deposits situated near the medial canthus, associated in $50\%$ of cases with hypercholesterolemia or other systemic metabolic conditions.

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Seborrheic keratosis

Common benign skin growth caused by proliferation of immature keratinocytes, presenting as a well-defined, slow-growing, greasy brown 'stuck-on' plaque.

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Capillary hemangioma

Common benign pediatric vascular tumor presenting as a raised red or purple eyelid lesion that blanches with pressure and swells during crying.

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Port-wine stain

Congenital dermal capillary malformation appearing as a flat pink-to-purple patch along the trigeminal nerve distribution that does not blanch with pressure.

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Nevus of Ota

Congenital oculodermal melanosis presenting with slate grey-blue hyperpigmentation along $V_1$/$V_2$ branches and ipsilateral scleral hyperpigmentation.

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Junctional nevus

Flat, pigmented plaque appearing in childhood with nevus cells confined to the dermal-epidermal junction.

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Compound nevus

Elevated, papular, pigmented lesion appearing during puberty with nevus cells in both the junctional and dermal layers.

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Intradermal nevus

Elevated, flesh-colored or lightly pigmented lesion appearing in adulthood with nevus cells confined entirely within the dermis.

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Actinic keratosis

Flat, scaly, erythematous precancerous skin lesion caused by chronic UV exposure that serves as a direct precursor to Squamous Cell Carcinoma.

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Basal cell carcinoma

The most common eyelid cancer, presenting as a firm, locally invasive nodule with pearly raised borders, central ulceration, and surface telangiectasia.

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Squamous cell carcinoma

Invasive eyelid cancer arising from epidermal keratinocytes, presenting as a firm hyperkeratotic nodule or ulceration lacking surface telangiectasia.

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Kaposi sarcoma

Vascular malignancy caused by Human Herpesvirus 8 (HHV-8) in immunocompromised patients, presenting as elevated purple eyelid or conjunctival lesions.

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Merkel cell carcinoma

Rare, highly aggressive neuroendocrine skin cancer presenting as a painless, fast-growing red or pink upper eyelid nodule with a high rate ($30\%$) of metastasis.

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Marcus Gunn jaw-winking syndrome

Congenital neurogenic ptosis caused by aberrant innervation of the levator muscle by the motor branch of the trigeminal nerve ($V_3$), resulting in upper lid retraction during jaw movements.

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Pseudoptosis

False impression of eyelid drooping despite normal levator function and lid margin position, caused by dermatochalasis, lack of globe support, or contralateral lid retraction.

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Dermatochalasis

Age-related excess, redundant, and lax upper or lower eyelid skin that sags over the lid margin and can obstruct the superior visual field.

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Epiblepharon

Congenital condition where a horizontal fold of redundant skin and hypertrophied orbicularis muscle pushes the lower eyelashes inward against the globe while the eyelid margin remains normally positioned.

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Entropion

Inward inversion of the eyelid margin toward the globe, causing eyelashes and skin to rub against the cornea.

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Ectropion

Outward eversion of the eyelid margin away from the globe, exposing the palpebral conjunctiva and leading to tear evaporation and epiphora.

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Lagophthalmos

Inability to fully close the eyelids, causing inferior scleral show during closure, exposure keratopathy, and nocturnal corneal drying.

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Floppy eyelid syndrome

Bilateral condition characterized by extreme lid laxity and rubbery tarsal plates, causing spontaneous lid eversion during sleep; strongly associated with obstructive sleep apnea.

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Blepharospasm

Involuntary, bilateral, forcible contraction or spasm of the orbicularis oculi and surrounding facial muscles.

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Eyelid myokymia

Benign, self-limiting fine twitching of the orbicularis oculi muscle, typically triggered by stress, fatigue, or excess caffeine intake.

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Epicanthal folds

Vertical skin folds covering the inner canthus, creating a false appearance of esotropia (pseudoesotropia) in infants or Asian individuals.

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Congenital coloboma

Full-thickness notch or defect in the eyelid margin resulting from failure of embryological lid development and fusion.

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Thyroid eye disease

Autoimmune inflammatory condition affecting orbital fat and extraocular muscles, presenting with upper eyelid retraction, lagophthalmos, proptosis, and extraocular muscle restriction.

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Ocular rosacea

Chronic inflammatory condition affecting the eyelids and ocular surface, featuring meibomian gland capping, lid telangiectasia, and facial erythema.

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Sturge-Weber syndrome

Congenital neurocutaneous disorder combining a facial port-wine stain along V1 with leptomeningeal vascular malformations, seizures, and glaucoma.