An acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiology

This case report describes a patient with acute posterior multifocal placoid pigment epitheliopathy, presumed to be the initial manifestation of systemic lupus erythematosus (SLE), who responded to oral immunotherapy. The clinical, hematological, serological, and imaging examinations were carried ou...

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Main Author: Omer Othman Abdullah
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2025-01-01
Series:Oman Journal of Ophthalmology
Subjects:
Online Access:https://journals.lww.com/10.4103/ojo.ojo_188_23
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author Omer Othman Abdullah
author_facet Omer Othman Abdullah
author_sort Omer Othman Abdullah
collection DOAJ
description This case report describes a patient with acute posterior multifocal placoid pigment epitheliopathy, presumed to be the initial manifestation of systemic lupus erythematosus (SLE), who responded to oral immunotherapy. The clinical, hematological, serological, and imaging examinations were carried out on the 28-year-old female who presented with bilateral multifocal central creamy lesions. The imaging modalities’ findings and the overall visual improvement led us to diagnose acute posterior multifocal placoid pigmented epitheliopathy. This is the second time SLE has been presented as acute posterior multifocal placoid pigmented epitheliopathy, and before declaring it is idiopathic, we must investigate it thoroughly.
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spelling doaj-art-c1ce43eb52e944388a938b7e9fdec7182025-08-20T02:04:51ZengWolters Kluwer Medknow PublicationsOman Journal of Ophthalmology0974-620X0974-78422025-01-01181515410.4103/ojo.ojo_188_23An acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiologyOmer Othman AbdullahThis case report describes a patient with acute posterior multifocal placoid pigment epitheliopathy, presumed to be the initial manifestation of systemic lupus erythematosus (SLE), who responded to oral immunotherapy. The clinical, hematological, serological, and imaging examinations were carried out on the 28-year-old female who presented with bilateral multifocal central creamy lesions. The imaging modalities’ findings and the overall visual improvement led us to diagnose acute posterior multifocal placoid pigmented epitheliopathy. This is the second time SLE has been presented as acute posterior multifocal placoid pigmented epitheliopathy, and before declaring it is idiopathic, we must investigate it thoroughly.https://journals.lww.com/10.4103/ojo.ojo_188_23acute posterior multifocal placoid pigment epitheliopathycase reportsystemic lupus erythematosus
spellingShingle Omer Othman Abdullah
An acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiology
Oman Journal of Ophthalmology
acute posterior multifocal placoid pigment epitheliopathy
case report
systemic lupus erythematosus
title An acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiology
title_full An acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiology
title_fullStr An acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiology
title_full_unstemmed An acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiology
title_short An acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiology
title_sort acute posterior multifocal placoid pigment epitheliopathy with presumed systemic lupus erythematosus etiology
topic acute posterior multifocal placoid pigment epitheliopathy
case report
systemic lupus erythematosus
url https://journals.lww.com/10.4103/ojo.ojo_188_23
work_keys_str_mv AT omerothmanabdullah anacuteposteriormultifocalplacoidpigmentepitheliopathywithpresumedsystemiclupuserythematosusetiology
AT omerothmanabdullah acuteposteriormultifocalplacoidpigmentepitheliopathywithpresumedsystemiclupuserythematosusetiology