Ocular Cicatricial Pemphigoid in a Healthy Elderly Male Filipino Patient

Ocular cicatricial pemphigoid (OCP) is a chronic bilateral, blinding, cicatrizing form of conjunctivitis with relapsing and remitting periods. It has strong evidence for an immune type II hypersensitivity that leads to subconjunctival fibrosis and extensive systemic bullae formation. To the best knowledge of the authors, this is the first reported case of direct immunofluorescence (DIF) assay-proven OCP in an elderly Filipino man. A 68-year-old male presented with bilateral corneal conjunctivalization, symblepharon, ectropion, conjunctival hyperemia testing positive with conjunctival biopsy for basement membrane antibodies with DIF for the left eye, while turning out negative for the right eye. He was managed as a case of OCP, both eyes, and was given topical steroids and antibiotics. Oral Dapsone was started by Dermatology and Rheumatology Services. OCP is a rare autoimmune and blinding disease. Early diagnosis and prompt treatment are vital as ocular complications permanently affect the quality of life of patients as seen in our patient. DIF assay remains the gold-standard for diagnosis. Systemic immunosuppression is the mainstay of treatment. Adjunctive supportive topical medication may be given to alleviate ocular discomfort. A multidisciplinary approach is essential to provide holistic care to each patient.

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Publication Details

Journal
Acta Medica Philippina
Published
2025-01-01
DOI
https://doi.org/10.47895/amp.vi0.12049
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
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article

Ocular Cicatricial Pemphigoid in a Healthy Elderly Male Filipino Patient

Acta Medica Philippina
Autoimmune Bullous Skin Diseases
article

Ocular Cicatricial Pemphigoid in a Healthy Elderly Male Filipino Patient

article en

Abstract

Ocular cicatricial pemphigoid (OCP) is a chronic bilateral, blinding, cicatrizing form of conjunctivitis with relapsing and remitting periods. It has strong evidence for an immune type II hypersensitivity that leads to subconjunctival fibrosis and extensive systemic bullae formation. To the best knowledge of the authors, this is the first reported case of direct immunofluorescence (DIF) assay-proven OCP in an elderly Filipino man. A 68-year-old male presented with bilateral corneal conjunctivalization, symblepharon, ectropion, conjunctival hyperemia testing positive with conjunctival biopsy for basement membrane antibodies with DIF for the left eye, while turning out negative for the right eye. He was managed as a case of OCP, both eyes, and was given topical steroids and antibiotics. Oral Dapsone was started by Dermatology and Rheumatology Services. OCP is a rare autoimmune and blinding disease. Early diagnosis and prompt treatment are vital as ocular complications permanently affect the quality of life of patients as seen in our patient. DIF assay remains the gold-standard for diagnosis. Systemic immunosuppression is the mainstay of treatment. Adjunctive supportive topical medication may be given to alleviate ocular discomfort. A multidisciplinary approach is essential to provide holistic care to each patient.

Acta Medica PhilippinaVol. 59(18)
Philippine General Hospital (PH), St. Luke's Medical Center (PH), University of the Philippines Manila (PH)
Gender equality
Openalex Percentile: Top 92%
Autoimmune Bullous Skin Diseases
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Ocular Cicatricial Pemphigoid in a Healthy Elderly Male Filipino Patient · Acta Medica Philippina (2025) | TGRS Research Map | TGRS