Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case Report

<i>Introduction</i>. Leber hereditary optic neuropathy (LHON) is a condition characterized by bilateral acute or subacute vision loss in seemingly healthy individuals. Depending on the disease stage and initial presentation, it is often diagnosed as optic neuritis. Elevated levels of end...

Full description

Saved in:
Bibliographic Details
Main Authors: Lepsa Zoric, Aleksandra Petrovic, Vladimir Milutinovic
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Medicina
Subjects:
Online Access:https://www.mdpi.com/1648-9144/61/1/7
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832588031962382336
author Lepsa Zoric
Aleksandra Petrovic
Vladimir Milutinovic
author_facet Lepsa Zoric
Aleksandra Petrovic
Vladimir Milutinovic
author_sort Lepsa Zoric
collection DOAJ
description <i>Introduction</i>. Leber hereditary optic neuropathy (LHON) is a condition characterized by bilateral acute or subacute vision loss in seemingly healthy individuals. Depending on the disease stage and initial presentation, it is often diagnosed as optic neuritis. Elevated levels of endogenous and exogenous glucocorticoids have been associated with the onset of central serous chorioretinopathy (CSCR). In our patient, CSCR developed after only three days of pulse corticosteroid therapy, prescribed due to initial presentation as bilateral optic neuritis (papillitis). <i>Objective</i>. Through our case report, we aimed to highlight that CSCR can develop after the initiation of pulse corticosteroid therapy in a patient with LHON and to propose choroidal thickness as a potential contributing factor for this complication. <i>Case Presentation</i>. A 27-year-old male patient presented with painless subacute vision loss in both eyes. The decline in vision developed gradually over 20 days, prior to the patient’s referral to the UKCS Eye Disease Clinic for further examination and treatment, and was not accompanied by pain during eye movements. Initial investigations upon admission to the clinic established the diagnosis of optic neuritis. Consequently, pulse corticosteroid therapy was administered. Three days after the initiation of intravenous methylprednisolone, the patient developed bilateral central serous chorioretinopathy. After cessation of therapy, there was a rapid resolution of choroidopathy, but no improvement in visual acuity, prompting genetic testing. Subsequent laboratory results revealed a positive test for the LHON mutation m.3460 G>A (MT-ND1). <i>Conclusions</i>. LHON is often misdiagnosed as optic neuritis, as upon initial presentation the optic nerve disk often does not exhibit the apparent characteristics of LHON. Numerous studies have documented the development of central serous chorioretinopathy following corticosteroid treatment, though none have reported the onset of CSCR after only three days of pulse corticosteroid therapy. Increased choroidal thickness is a characteristic of the acute phase of LHON and may be associated with the development of CSCR in our patient.
format Article
id doaj-art-f463dd045d954b7aa9e139032ae053f4
institution Kabale University
issn 1010-660X
1648-9144
language English
publishDate 2024-12-01
publisher MDPI AG
record_format Article
series Medicina
spelling doaj-art-f463dd045d954b7aa9e139032ae053f42025-01-24T13:40:13ZengMDPI AGMedicina1010-660X1648-91442024-12-01611710.3390/medicina61010007Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case ReportLepsa Zoric0Aleksandra Petrovic1Vladimir Milutinovic2School of Medicine, University of Pristina, 38220 Kosovska Mitrovica, SerbiaHealth Center Dr Milutin Ivkovic, 11000 Belgrade, SerbiaClinic for Eye Disease, University Clinical Center of Serbia, 11000 Belgrade, Serbia<i>Introduction</i>. Leber hereditary optic neuropathy (LHON) is a condition characterized by bilateral acute or subacute vision loss in seemingly healthy individuals. Depending on the disease stage and initial presentation, it is often diagnosed as optic neuritis. Elevated levels of endogenous and exogenous glucocorticoids have been associated with the onset of central serous chorioretinopathy (CSCR). In our patient, CSCR developed after only three days of pulse corticosteroid therapy, prescribed due to initial presentation as bilateral optic neuritis (papillitis). <i>Objective</i>. Through our case report, we aimed to highlight that CSCR can develop after the initiation of pulse corticosteroid therapy in a patient with LHON and to propose choroidal thickness as a potential contributing factor for this complication. <i>Case Presentation</i>. A 27-year-old male patient presented with painless subacute vision loss in both eyes. The decline in vision developed gradually over 20 days, prior to the patient’s referral to the UKCS Eye Disease Clinic for further examination and treatment, and was not accompanied by pain during eye movements. Initial investigations upon admission to the clinic established the diagnosis of optic neuritis. Consequently, pulse corticosteroid therapy was administered. Three days after the initiation of intravenous methylprednisolone, the patient developed bilateral central serous chorioretinopathy. After cessation of therapy, there was a rapid resolution of choroidopathy, but no improvement in visual acuity, prompting genetic testing. Subsequent laboratory results revealed a positive test for the LHON mutation m.3460 G>A (MT-ND1). <i>Conclusions</i>. LHON is often misdiagnosed as optic neuritis, as upon initial presentation the optic nerve disk often does not exhibit the apparent characteristics of LHON. Numerous studies have documented the development of central serous chorioretinopathy following corticosteroid treatment, though none have reported the onset of CSCR after only three days of pulse corticosteroid therapy. Increased choroidal thickness is a characteristic of the acute phase of LHON and may be associated with the development of CSCR in our patient.https://www.mdpi.com/1648-9144/61/1/7Leber hereditary optic neuropathy (LHON)central serous chorioretinopathy (CSCR)corticosteroid therapy
spellingShingle Lepsa Zoric
Aleksandra Petrovic
Vladimir Milutinovic
Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case Report
Medicina
Leber hereditary optic neuropathy (LHON)
central serous chorioretinopathy (CSCR)
corticosteroid therapy
title Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case Report
title_full Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case Report
title_fullStr Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case Report
title_full_unstemmed Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case Report
title_short Central Serous Chorioretinopathy Associated with Corticosteroid Use in a Patient with Leber Hereditary Optic Neuropathy: A Case Report
title_sort central serous chorioretinopathy associated with corticosteroid use in a patient with leber hereditary optic neuropathy a case report
topic Leber hereditary optic neuropathy (LHON)
central serous chorioretinopathy (CSCR)
corticosteroid therapy
url https://www.mdpi.com/1648-9144/61/1/7
work_keys_str_mv AT lepsazoric centralserouschorioretinopathyassociatedwithcorticosteroiduseinapatientwithleberhereditaryopticneuropathyacasereport
AT aleksandrapetrovic centralserouschorioretinopathyassociatedwithcorticosteroiduseinapatientwithleberhereditaryopticneuropathyacasereport
AT vladimirmilutinovic centralserouschorioretinopathyassociatedwithcorticosteroiduseinapatientwithleberhereditaryopticneuropathyacasereport