Cargando…

Ocular Involvement and Blindness Secondary to Linear IgA Dermatosis

A 43-year-old man with linear immunoglobulin A (IgA) dermatosis associated with gluten intolerance presented with progressive vision loss, pain and photosensitivity in both eyes. His visual acuity was light perception (LP) in both eyes. A physical examination revealed bullous, papular lesions with e...

Descripción completa

Detalles Bibliográficos
Autores principales: Ramos-Castellón, Cinthya, Ortiz-Nieva, Gabriela, Fresán, Fernando, Villalvazo, Leonardo, Garfias, Yonathan, Navas, Alejandro, Jiménez-Martínez, María C.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017945/
https://www.ncbi.nlm.nih.gov/pubmed/21234343
http://dx.doi.org/10.1155/2010/280396
_version_ 1782195991186767872
author Ramos-Castellón, Cinthya
Ortiz-Nieva, Gabriela
Fresán, Fernando
Villalvazo, Leonardo
Garfias, Yonathan
Navas, Alejandro
Jiménez-Martínez, María C.
author_facet Ramos-Castellón, Cinthya
Ortiz-Nieva, Gabriela
Fresán, Fernando
Villalvazo, Leonardo
Garfias, Yonathan
Navas, Alejandro
Jiménez-Martínez, María C.
author_sort Ramos-Castellón, Cinthya
collection PubMed
description A 43-year-old man with linear immunoglobulin A (IgA) dermatosis associated with gluten intolerance presented with progressive vision loss, pain and photosensitivity in both eyes. His visual acuity was light perception (LP) in both eyes. A physical examination revealed bullous, papular lesions with erythematous borders in periocular tissues, limbs, and thorax. Slit-lamp examination showed conjunctival hyperemia, fibrosis, corneal opacification, and vascularization with epithelial defects. Immunofluorescent skin and corneal surface biopsy studies showed linear IgA deposits. The patient was treated with keratolimbal allogenic transplantation and cryopreserved amniotic membrane in the right eye. Regardless of the treatment he persisted with torpid evolution developing retinal and choroidal detachments. After these events he was started on intravenous immune globulin (IVIG) and showed very slight improvement in ocular surface. These types of blistering diseases are rare in the eye. Even when adequate local treatment is given, systemic treatment is mandatory and ocular prognosis can be unsatisfactory.
format Text
id pubmed-3017945
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-30179452011-01-13 Ocular Involvement and Blindness Secondary to Linear IgA Dermatosis Ramos-Castellón, Cinthya Ortiz-Nieva, Gabriela Fresán, Fernando Villalvazo, Leonardo Garfias, Yonathan Navas, Alejandro Jiménez-Martínez, María C. J Ophthalmol Case Report A 43-year-old man with linear immunoglobulin A (IgA) dermatosis associated with gluten intolerance presented with progressive vision loss, pain and photosensitivity in both eyes. His visual acuity was light perception (LP) in both eyes. A physical examination revealed bullous, papular lesions with erythematous borders in periocular tissues, limbs, and thorax. Slit-lamp examination showed conjunctival hyperemia, fibrosis, corneal opacification, and vascularization with epithelial defects. Immunofluorescent skin and corneal surface biopsy studies showed linear IgA deposits. The patient was treated with keratolimbal allogenic transplantation and cryopreserved amniotic membrane in the right eye. Regardless of the treatment he persisted with torpid evolution developing retinal and choroidal detachments. After these events he was started on intravenous immune globulin (IVIG) and showed very slight improvement in ocular surface. These types of blistering diseases are rare in the eye. Even when adequate local treatment is given, systemic treatment is mandatory and ocular prognosis can be unsatisfactory. Hindawi Publishing Corporation 2010 2010-12-22 /pmc/articles/PMC3017945/ /pubmed/21234343 http://dx.doi.org/10.1155/2010/280396 Text en Copyright © 2010 Cinthya Ramos-Castellón et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ramos-Castellón, Cinthya
Ortiz-Nieva, Gabriela
Fresán, Fernando
Villalvazo, Leonardo
Garfias, Yonathan
Navas, Alejandro
Jiménez-Martínez, María C.
Ocular Involvement and Blindness Secondary to Linear IgA Dermatosis
title Ocular Involvement and Blindness Secondary to Linear IgA Dermatosis
title_full Ocular Involvement and Blindness Secondary to Linear IgA Dermatosis
title_fullStr Ocular Involvement and Blindness Secondary to Linear IgA Dermatosis
title_full_unstemmed Ocular Involvement and Blindness Secondary to Linear IgA Dermatosis
title_short Ocular Involvement and Blindness Secondary to Linear IgA Dermatosis
title_sort ocular involvement and blindness secondary to linear iga dermatosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017945/
https://www.ncbi.nlm.nih.gov/pubmed/21234343
http://dx.doi.org/10.1155/2010/280396
work_keys_str_mv AT ramoscastelloncinthya ocularinvolvementandblindnesssecondarytolinearigadermatosis
AT ortiznievagabriela ocularinvolvementandblindnesssecondarytolinearigadermatosis
AT fresanfernando ocularinvolvementandblindnesssecondarytolinearigadermatosis
AT villalvazoleonardo ocularinvolvementandblindnesssecondarytolinearigadermatosis
AT garfiasyonathan ocularinvolvementandblindnesssecondarytolinearigadermatosis
AT navasalejandro ocularinvolvementandblindnesssecondarytolinearigadermatosis
AT jimenezmartinezmariac ocularinvolvementandblindnesssecondarytolinearigadermatosis