Adalimumab-induced optic neuropathy in a patient with Behçet’s syndrome

A 37-year-old woman with a diagnosis of Behçet’s syndrome, treated with colchicine and prednisolone, maintained low disease activity for a period of 10 years, after which, she developed a new episode of anterior uveitis. A cycle of high dose systemic corticosteroids was required but the patient pres...

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Main Authors: Sofia Miranda, Daniel Calado, Joana Rua, Fernando Salvador
Format: Article
Language:English
Published: SMC MEDIA SRL 2025-01-01
Series:European Journal of Case Reports in Internal Medicine
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Online Access:https://www.ejcrim.com/index.php/EJCRIM/article/view/5112
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author Sofia Miranda
Daniel Calado
Joana Rua
Fernando Salvador
author_facet Sofia Miranda
Daniel Calado
Joana Rua
Fernando Salvador
author_sort Sofia Miranda
collection DOAJ
description A 37-year-old woman with a diagnosis of Behçet’s syndrome, treated with colchicine and prednisolone, maintained low disease activity for a period of 10 years, after which, she developed a new episode of anterior uveitis. A cycle of high dose systemic corticosteroids was required but the patient presented with a new flare during dose tapering. A decision to initiate a corticosteroid-sparing agent was then made, with an initially satisfactory response. However, 3 months later the ocular symptoms recurred, and a new bout of oral ulceration appeared concurrently. As a result, adalimumab was then started, but the patient presented with a sudden and severe decrease of visual acuity in her right eye 4 months later. The initial bloodwork showed no elevated inflammatory markers. A lumbar puncture showed a normal cerebrospinal fluid composition. Although these findings made it less probable that the patient’s symptoms were caused by infectious or autoimmune disease, extensive investigations directed at these possible causes were performed, with negative results. Several imaging tests were also performed, which showed no alterations. However, a sensory evoked potentials test revealed a functional compromise at the pre-chiasmatic level. An iatrogenic optic neuropathy induced by adalimumab seemed the most probable cause and a decision to suspend the treatment was made. A new cycle of high dose systemic corticosteroids consisting of three pulses of methylprednisolone followed by pred-nisolone with a quick tapering over 4 weeks was also started, with gradual improvement of visual acuity.
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spelling doaj-art-261fd81b9d4344ee94890db49930498d2025-02-04T13:37:20ZengSMC MEDIA SRLEuropean Journal of Case Reports in Internal Medicine2284-25942025-01-0110.12890/2025_0051124647Adalimumab-induced optic neuropathy in a patient with Behçet’s syndromeSofia Miranda0Daniel Calado1Joana Rua2Fernando Salvador3Internal Medicine Department, Hospital do Divino Espírito Santo, Ponta Delgada, PortugalInternal Medicine Department, Hospital do Divino Espírito Santo, Ponta Delgada, PortugalInternal Medicine Department, Unidade Local de Saúde de Trás-os-Montes e Alto Douro, Vila Real, PortugalInternal Medicine Department, Unidade Local de Saúde de Trás-os-Montes e Alto Douro, Vila Real, PortugalA 37-year-old woman with a diagnosis of Behçet’s syndrome, treated with colchicine and prednisolone, maintained low disease activity for a period of 10 years, after which, she developed a new episode of anterior uveitis. A cycle of high dose systemic corticosteroids was required but the patient presented with a new flare during dose tapering. A decision to initiate a corticosteroid-sparing agent was then made, with an initially satisfactory response. However, 3 months later the ocular symptoms recurred, and a new bout of oral ulceration appeared concurrently. As a result, adalimumab was then started, but the patient presented with a sudden and severe decrease of visual acuity in her right eye 4 months later. The initial bloodwork showed no elevated inflammatory markers. A lumbar puncture showed a normal cerebrospinal fluid composition. Although these findings made it less probable that the patient’s symptoms were caused by infectious or autoimmune disease, extensive investigations directed at these possible causes were performed, with negative results. Several imaging tests were also performed, which showed no alterations. However, a sensory evoked potentials test revealed a functional compromise at the pre-chiasmatic level. An iatrogenic optic neuropathy induced by adalimumab seemed the most probable cause and a decision to suspend the treatment was made. A new cycle of high dose systemic corticosteroids consisting of three pulses of methylprednisolone followed by pred-nisolone with a quick tapering over 4 weeks was also started, with gradual improvement of visual acuity.https://www.ejcrim.com/index.php/EJCRIM/article/view/5112adalimumaboptic neuropathy
spellingShingle Sofia Miranda
Daniel Calado
Joana Rua
Fernando Salvador
Adalimumab-induced optic neuropathy in a patient with Behçet’s syndrome
European Journal of Case Reports in Internal Medicine
adalimumab
optic neuropathy
title Adalimumab-induced optic neuropathy in a patient with Behçet’s syndrome
title_full Adalimumab-induced optic neuropathy in a patient with Behçet’s syndrome
title_fullStr Adalimumab-induced optic neuropathy in a patient with Behçet’s syndrome
title_full_unstemmed Adalimumab-induced optic neuropathy in a patient with Behçet’s syndrome
title_short Adalimumab-induced optic neuropathy in a patient with Behçet’s syndrome
title_sort adalimumab induced optic neuropathy in a patient with behcet s syndrome
topic adalimumab
optic neuropathy
url https://www.ejcrim.com/index.php/EJCRIM/article/view/5112
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AT joanarua adalimumabinducedopticneuropathyinapatientwithbehcetssyndrome
AT fernandosalvador adalimumabinducedopticneuropathyinapatientwithbehcetssyndrome