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Classical Pathology of Sympathetic Ophthalmia Presented in a Unique Case

The ocular pathology of sympathetic ophthalmia is demonstrated in a 10 year-old boy who sustained a penetrating left globe injury and subsequently developed sympathetic ophthalmia in the right eye two months later. Two and a half weeks following extensive surgical repair of the left ruptured globe,...

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Autores principales: Chen, Shida, Aronow, Mary E, Wang, Charles, Shen, Defen, Chan, Chi-Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4110402/
https://www.ncbi.nlm.nih.gov/pubmed/25067979
http://dx.doi.org/10.2174/1874364101408010032
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author Chen, Shida
Aronow, Mary E
Wang, Charles
Shen, Defen
Chan, Chi-Chao
author_facet Chen, Shida
Aronow, Mary E
Wang, Charles
Shen, Defen
Chan, Chi-Chao
author_sort Chen, Shida
collection PubMed
description The ocular pathology of sympathetic ophthalmia is demonstrated in a 10 year-old boy who sustained a penetrating left globe injury and subsequently developed sympathetic ophthalmia in the right eye two months later. Two and a half weeks following extensive surgical repair of the left ruptured globe, he developed endophthalmitis and was treated with oral and topical fortified antibiotics. One month after the initial injury, a progressive corneal ulcer of the left eye led to perforation and the need for emergent corneal transplantation. The surgical specimen revealed fungus, Scedosporium dehoogii. The boy received systemic and topical anti-fungal therapy. Two months following the penetrating globe injury of the left eye, a granulomatous uveitis developed in the right eye. Sympathetic ophthalmia was suspected and the patient began treatment with topical and oral corticosteroids. Given the concern of vision loss secondary to sympathetic ophthalmia in the right eye, as well as poor vision and hypotony in the injured eye, the left eye was enucleated. Microscopically, granulomatous inflammation with giant cells was noted within a cyclitic membrane which filled the anterior and posterior chamber of the left globe. Other classic features including Dalen-Fuchs nodules were identified. Small, choroidal, ill-defined granulomas and relative sparing of the choriocapillaris were present. Molecular analysis did not identify evidence of remaining fungal infection. The pathology findings were consistent with previously described features of sympathetic ophthalmia. The present case is unique in that co-existing fungal infection may have potentiated the risk for developing sympathetic ophthalmia in the fellow eye.
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spelling pubmed-41104022014-07-25 Classical Pathology of Sympathetic Ophthalmia Presented in a Unique Case Chen, Shida Aronow, Mary E Wang, Charles Shen, Defen Chan, Chi-Chao Open Ophthalmol J Article The ocular pathology of sympathetic ophthalmia is demonstrated in a 10 year-old boy who sustained a penetrating left globe injury and subsequently developed sympathetic ophthalmia in the right eye two months later. Two and a half weeks following extensive surgical repair of the left ruptured globe, he developed endophthalmitis and was treated with oral and topical fortified antibiotics. One month after the initial injury, a progressive corneal ulcer of the left eye led to perforation and the need for emergent corneal transplantation. The surgical specimen revealed fungus, Scedosporium dehoogii. The boy received systemic and topical anti-fungal therapy. Two months following the penetrating globe injury of the left eye, a granulomatous uveitis developed in the right eye. Sympathetic ophthalmia was suspected and the patient began treatment with topical and oral corticosteroids. Given the concern of vision loss secondary to sympathetic ophthalmia in the right eye, as well as poor vision and hypotony in the injured eye, the left eye was enucleated. Microscopically, granulomatous inflammation with giant cells was noted within a cyclitic membrane which filled the anterior and posterior chamber of the left globe. Other classic features including Dalen-Fuchs nodules were identified. Small, choroidal, ill-defined granulomas and relative sparing of the choriocapillaris were present. Molecular analysis did not identify evidence of remaining fungal infection. The pathology findings were consistent with previously described features of sympathetic ophthalmia. The present case is unique in that co-existing fungal infection may have potentiated the risk for developing sympathetic ophthalmia in the fellow eye. Bentham Open 2014-06-27 /pmc/articles/PMC4110402/ /pubmed/25067979 http://dx.doi.org/10.2174/1874364101408010032 Text en © Chen et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Chen, Shida
Aronow, Mary E
Wang, Charles
Shen, Defen
Chan, Chi-Chao
Classical Pathology of Sympathetic Ophthalmia Presented in a Unique Case
title Classical Pathology of Sympathetic Ophthalmia Presented in a Unique Case
title_full Classical Pathology of Sympathetic Ophthalmia Presented in a Unique Case
title_fullStr Classical Pathology of Sympathetic Ophthalmia Presented in a Unique Case
title_full_unstemmed Classical Pathology of Sympathetic Ophthalmia Presented in a Unique Case
title_short Classical Pathology of Sympathetic Ophthalmia Presented in a Unique Case
title_sort classical pathology of sympathetic ophthalmia presented in a unique case
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4110402/
https://www.ncbi.nlm.nih.gov/pubmed/25067979
http://dx.doi.org/10.2174/1874364101408010032
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