Ocular cicatricial pemphigoid secondary to intravitreal implant of ranibizumab: a case report
Purpose Mucous membrane pemphigoid is a systemic disorder that primarily affects mucous membranes. When localized to conjunctiva, it is know as ocular cicatricial pemphigoid (OCP), a potentially blinding desease resulting in progressive conjunctival fibrosis and ocular surface failure.Women are affe...
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creator | López Sangrós, I. Marco Monzón, S. Bartolomé Sensé, I. Berniolles Alcalde, J. Sanchez Marin, J.I. Idoate Domenech, A. Ascaso Puyuelo, J. Del Buey Sallas, M.A. |
description | Purpose
Mucous membrane pemphigoid is a systemic disorder that primarily affects mucous membranes. When localized to conjunctiva, it is know as ocular cicatricial pemphigoid (OCP), a potentially blinding desease resulting in progressive conjunctival fibrosis and ocular surface failure.Women are affected more than men by a ratio of 8:1. Age on onset is usually age 60 to 80 and rarely younger than 30. We describe the case of a patient with OCP secondary to intravitreal implant of ranibizumab.
Methods
We describe the case of a patient with OCP secondary to intravitreal implant of ranibizumab.
Results
A 85 years old woman with bilateral macular degeneration, treated with intravitreal implants of ranibizumab in the right eye, began with a non specific queratoconjunctivitis in the right eye after the second administration of intravitreal ranibizumab. In numerous ophthalmology follow‐ up appointments the patient presented red right eye and increased amount of tears. Six months later, after another intravitreal implant of ranibizumab, the patient presented a subepithelial fibrosis, as fine gray‐white striae in the inferior fornix. The patient was treated with topic corticosteroid, cyclosporin 0,2%, autologous serum eye 20% with a significant improvement. A systemic treatment with 15 mg methotrexate once a week and the suspension of intravitreal implants of ranibizumab was necessary to control the progression of the OCP.
Conclusions
In some patients, systemic drugs (practolol, D penicilamine…), have triggered the onset of OCP. The term pseudopemphigoid or drug‐induced pemphigoid may be used to describe these cases. There are not cases of POC secondary to ranibizumab described on the literature. |
doi_str_mv | 10.1111/j.1755-3768.2017.0S016 |
format | Article |
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Mucous membrane pemphigoid is a systemic disorder that primarily affects mucous membranes. When localized to conjunctiva, it is know as ocular cicatricial pemphigoid (OCP), a potentially blinding desease resulting in progressive conjunctival fibrosis and ocular surface failure.Women are affected more than men by a ratio of 8:1. Age on onset is usually age 60 to 80 and rarely younger than 30. We describe the case of a patient with OCP secondary to intravitreal implant of ranibizumab.
Methods
We describe the case of a patient with OCP secondary to intravitreal implant of ranibizumab.
Results
A 85 years old woman with bilateral macular degeneration, treated with intravitreal implants of ranibizumab in the right eye, began with a non specific queratoconjunctivitis in the right eye after the second administration of intravitreal ranibizumab. In numerous ophthalmology follow‐ up appointments the patient presented red right eye and increased amount of tears. Six months later, after another intravitreal implant of ranibizumab, the patient presented a subepithelial fibrosis, as fine gray‐white striae in the inferior fornix. The patient was treated with topic corticosteroid, cyclosporin 0,2%, autologous serum eye 20% with a significant improvement. A systemic treatment with 15 mg methotrexate once a week and the suspension of intravitreal implants of ranibizumab was necessary to control the progression of the OCP.
Conclusions
In some patients, systemic drugs (practolol, D penicilamine…), have triggered the onset of OCP. The term pseudopemphigoid or drug‐induced pemphigoid may be used to describe these cases. There are not cases of POC secondary to ranibizumab described on the literature.</description><identifier>ISSN: 1755-375X</identifier><identifier>EISSN: 1755-3768</identifier><identifier>DOI: 10.1111/j.1755-3768.2017.0S016</identifier><language>eng</language><publisher>Malden: Wiley Subscription Services, Inc</publisher><subject>Case reports ; Conjunctiva ; Corticosteroids ; Eye ; Fibrosis ; Fornix ; Immunotherapy ; Macular degeneration ; Membranes ; Methotrexate ; Monoclonal antibodies ; Mucous membrane pemphigoid ; Ophthalmology ; Practolol ; Tears ; Transplants & implants</subject><ispartof>Acta ophthalmologica (Oxford, England), 2017-09, Vol.95 (S259), p.n/a</ispartof><rights>2017 The Authors Acta Ophthalmologica © 2017 Acta Ophthalmologica Scandinavica Foundation</rights><rights>Copyright © 2017 Acta Ophthalmologica Scandinavica Foundation</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1816-16143cd51eeb5d3bf365460aaf857b559e4bdbd7bb6672d051c6b4537aa6e5f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1755-3768.2017.0S016$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45551,46808</link.rule.ids></links><search><creatorcontrib>López Sangrós, I.</creatorcontrib><creatorcontrib>Marco Monzón, S.</creatorcontrib><creatorcontrib>Bartolomé Sensé, I.</creatorcontrib><creatorcontrib>Berniolles Alcalde, J.</creatorcontrib><creatorcontrib>Sanchez Marin, J.I.</creatorcontrib><creatorcontrib>Idoate Domenech, A.</creatorcontrib><creatorcontrib>Ascaso Puyuelo, J.</creatorcontrib><creatorcontrib>Del Buey Sallas, M.A.</creatorcontrib><title>Ocular cicatricial pemphigoid secondary to intravitreal implant of ranibizumab: a case report</title><title>Acta ophthalmologica (Oxford, England)</title><description>Purpose
Mucous membrane pemphigoid is a systemic disorder that primarily affects mucous membranes. When localized to conjunctiva, it is know as ocular cicatricial pemphigoid (OCP), a potentially blinding desease resulting in progressive conjunctival fibrosis and ocular surface failure.Women are affected more than men by a ratio of 8:1. Age on onset is usually age 60 to 80 and rarely younger than 30. We describe the case of a patient with OCP secondary to intravitreal implant of ranibizumab.
Methods
We describe the case of a patient with OCP secondary to intravitreal implant of ranibizumab.
Results
A 85 years old woman with bilateral macular degeneration, treated with intravitreal implants of ranibizumab in the right eye, began with a non specific queratoconjunctivitis in the right eye after the second administration of intravitreal ranibizumab. In numerous ophthalmology follow‐ up appointments the patient presented red right eye and increased amount of tears. Six months later, after another intravitreal implant of ranibizumab, the patient presented a subepithelial fibrosis, as fine gray‐white striae in the inferior fornix. The patient was treated with topic corticosteroid, cyclosporin 0,2%, autologous serum eye 20% with a significant improvement. A systemic treatment with 15 mg methotrexate once a week and the suspension of intravitreal implants of ranibizumab was necessary to control the progression of the OCP.
Conclusions
In some patients, systemic drugs (practolol, D penicilamine…), have triggered the onset of OCP. The term pseudopemphigoid or drug‐induced pemphigoid may be used to describe these cases. There are not cases of POC secondary to ranibizumab described on the literature.</description><subject>Case reports</subject><subject>Conjunctiva</subject><subject>Corticosteroids</subject><subject>Eye</subject><subject>Fibrosis</subject><subject>Fornix</subject><subject>Immunotherapy</subject><subject>Macular degeneration</subject><subject>Membranes</subject><subject>Methotrexate</subject><subject>Monoclonal antibodies</subject><subject>Mucous membrane pemphigoid</subject><subject>Ophthalmology</subject><subject>Practolol</subject><subject>Tears</subject><subject>Transplants & implants</subject><issn>1755-375X</issn><issn>1755-3768</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkE9LxDAQxYMouK5-BQl4bk3aZrIrXhbxHyzsYffgRUKSpprSNjVplfXT21rZs3OZYXhvHvND6JKSmA51XcaUMxalHBZxQiiPyZZQOEKzw_r4MLOXU3QWQkkIUIBshl43uq-kx9pq2Xmrraxwa-r23b45m-NgtGty6fe4c9g2nZeftvNmENm6rWTTYVdgLxur7HdfS3WDJdYyGOxN63x3jk4KWQVz8dfnaPdwv7t7itabx-e71TrSdEEhokCzVOeMGqNYnqoiBZYBkbJYMK4YW5pM5SrnSgHwJCeMalAZS7mUYFiRztHVdLb17qM3oROl630zJAq6TCFhyRAzqGBSae9C8KYQrbf18JugRIwkRSlGTGJEJkaS4pfkYLydjF-2Mvt_usRqs53sPy4bejU</recordid><startdate>201709</startdate><enddate>201709</enddate><creator>López Sangrós, I.</creator><creator>Marco Monzón, S.</creator><creator>Bartolomé Sensé, I.</creator><creator>Berniolles Alcalde, J.</creator><creator>Sanchez Marin, J.I.</creator><creator>Idoate Domenech, A.</creator><creator>Ascaso Puyuelo, J.</creator><creator>Del Buey Sallas, M.A.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>201709</creationdate><title>Ocular cicatricial pemphigoid secondary to intravitreal implant of ranibizumab: a case report</title><author>López Sangrós, I. ; Marco Monzón, S. ; Bartolomé Sensé, I. ; Berniolles Alcalde, J. ; Sanchez Marin, J.I. ; Idoate Domenech, A. ; Ascaso Puyuelo, J. ; Del Buey Sallas, M.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1816-16143cd51eeb5d3bf365460aaf857b559e4bdbd7bb6672d051c6b4537aa6e5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Case reports</topic><topic>Conjunctiva</topic><topic>Corticosteroids</topic><topic>Eye</topic><topic>Fibrosis</topic><topic>Fornix</topic><topic>Immunotherapy</topic><topic>Macular degeneration</topic><topic>Membranes</topic><topic>Methotrexate</topic><topic>Monoclonal antibodies</topic><topic>Mucous membrane pemphigoid</topic><topic>Ophthalmology</topic><topic>Practolol</topic><topic>Tears</topic><topic>Transplants & implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>López Sangrós, I.</creatorcontrib><creatorcontrib>Marco Monzón, S.</creatorcontrib><creatorcontrib>Bartolomé Sensé, I.</creatorcontrib><creatorcontrib>Berniolles Alcalde, J.</creatorcontrib><creatorcontrib>Sanchez Marin, J.I.</creatorcontrib><creatorcontrib>Idoate Domenech, A.</creatorcontrib><creatorcontrib>Ascaso Puyuelo, J.</creatorcontrib><creatorcontrib>Del Buey Sallas, M.A.</creatorcontrib><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Acta ophthalmologica (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>López Sangrós, I.</au><au>Marco Monzón, S.</au><au>Bartolomé Sensé, I.</au><au>Berniolles Alcalde, J.</au><au>Sanchez Marin, J.I.</au><au>Idoate Domenech, A.</au><au>Ascaso Puyuelo, J.</au><au>Del Buey Sallas, M.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ocular cicatricial pemphigoid secondary to intravitreal implant of ranibizumab: a case report</atitle><jtitle>Acta ophthalmologica (Oxford, England)</jtitle><date>2017-09</date><risdate>2017</risdate><volume>95</volume><issue>S259</issue><epage>n/a</epage><issn>1755-375X</issn><eissn>1755-3768</eissn><abstract>Purpose
Mucous membrane pemphigoid is a systemic disorder that primarily affects mucous membranes. When localized to conjunctiva, it is know as ocular cicatricial pemphigoid (OCP), a potentially blinding desease resulting in progressive conjunctival fibrosis and ocular surface failure.Women are affected more than men by a ratio of 8:1. Age on onset is usually age 60 to 80 and rarely younger than 30. We describe the case of a patient with OCP secondary to intravitreal implant of ranibizumab.
Methods
We describe the case of a patient with OCP secondary to intravitreal implant of ranibizumab.
Results
A 85 years old woman with bilateral macular degeneration, treated with intravitreal implants of ranibizumab in the right eye, began with a non specific queratoconjunctivitis in the right eye after the second administration of intravitreal ranibizumab. In numerous ophthalmology follow‐ up appointments the patient presented red right eye and increased amount of tears. Six months later, after another intravitreal implant of ranibizumab, the patient presented a subepithelial fibrosis, as fine gray‐white striae in the inferior fornix. The patient was treated with topic corticosteroid, cyclosporin 0,2%, autologous serum eye 20% with a significant improvement. A systemic treatment with 15 mg methotrexate once a week and the suspension of intravitreal implants of ranibizumab was necessary to control the progression of the OCP.
Conclusions
In some patients, systemic drugs (practolol, D penicilamine…), have triggered the onset of OCP. The term pseudopemphigoid or drug‐induced pemphigoid may be used to describe these cases. There are not cases of POC secondary to ranibizumab described on the literature.</abstract><cop>Malden</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/j.1755-3768.2017.0S016</doi><tpages>1</tpages></addata></record> |
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subjects | Case reports Conjunctiva Corticosteroids Eye Fibrosis Fornix Immunotherapy Macular degeneration Membranes Methotrexate Monoclonal antibodies Mucous membrane pemphigoid Ophthalmology Practolol Tears Transplants & implants |
title | Ocular cicatricial pemphigoid secondary to intravitreal implant of ranibizumab: a case report |
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