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Updated: Jun 2, 2026

Technique of Conjunctival Biopsy and Direct Immunofluorescence for Diagnosing Mucous Membrane Pemphigoid
Published on: June 17, 2025
Conjunctival erosions associated with pemphigus vulgaris
Rachel Brackley1, Jean Marie Pagani
1The Eye Institute at Pennsylvania College of Optometry at Salus University, Philadelphia, Pennsylvania, USA.
Purpose:
Pemphigus vulgaris (PV) is an autoimmune blistering disease that affects mucous membranes and the skin. Most commonly, the disease begins in the oral cavity and spreads to other areas including the conjunctiva and eyelids. Ocular involvement is rare and likely underdiagnosed with a frequency that is underestimated. Ocular manifestations of systemic PV can imply severe disease and require a multidisciplinary approach.
Case Report:
A 43-year-old black female presented with a chief complaint of pain with a white stringy discharge in the left eye for 2 weeks. On questioning, her health history revealed a 20-year systemic history of PV. Assessment of the anterior segment revealed diffuse conjunctival hyperemia with an area of bulbar conjunctival erosion. Based on the constellation of history, signs, and symptoms, ocular PV was diagnosed precipitating treatment for the ocular lesions and referral to the dermatologist for control of the underlying systemic condition.
Conclusions:
PV is an autoimmune disease of the pemphigus classification. It is characterized by the production of autoantibodies that attack intercellular substances. We review this unusual entity, its immunopathology, and treatment.
Insights
Ocular pemphigus vulgaris (PV) involves the eyes and is often underdiagnosed. Early diagnosis and multidisciplinary treatment are crucial for managing this rare autoimmune condition.
Area of Science:
- Ophthalmology
- Dermatology
- Autoimmunology
Background:
- Pemphigus vulgaris (PV) is a rare autoimmune blistering disease affecting skin and mucous membranes.
- Ocular involvement in PV is uncommon but can indicate severe systemic disease.
Observation:
- A case of a 43-year-old female with a 20-year history of systemic PV presenting with ocular symptoms.
- Clinical examination revealed conjunctival hyperemia and erosion in the left eye.
Findings:
- Diagnosis of ocular PV was made based on clinical presentation and patient history.
- The case highlights the importance of recognizing ocular manifestations of PV.
Implications:
- Ocular PV requires prompt diagnosis and a multidisciplinary approach involving ophthalmologists and dermatologists.
- Management focuses on treating ocular lesions and controlling the underlying systemic autoimmune condition.
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