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Amniotic membrane transplantation ineffective as additional therapy in patients with aggressive Mooren’s ulcer

BACKGROUND: Mooren’s ulcer is a severe ulcerative inflammation of the cornea. The exact pathogenesis remains unclear. Therefore many therapies of Mooren’s ulcer are recommended in literature. To shed more light on the ongoing question of optimal treatment of severe progressive Mooren’s ulcer, we her...

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Autores principales: Schallenberg, Maurice, Westekemper, Henrike, Steuhl, Klaus-Peter, Meller, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878411/
https://www.ncbi.nlm.nih.gov/pubmed/24345289
http://dx.doi.org/10.1186/1471-2415-13-81
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author Schallenberg, Maurice
Westekemper, Henrike
Steuhl, Klaus-Peter
Meller, Daniel
author_facet Schallenberg, Maurice
Westekemper, Henrike
Steuhl, Klaus-Peter
Meller, Daniel
author_sort Schallenberg, Maurice
collection PubMed
description BACKGROUND: Mooren’s ulcer is a severe ulcerative inflammation of the cornea. The exact pathogenesis remains unclear. Therefore many therapies of Mooren’s ulcer are recommended in literature. To shed more light on the ongoing question of optimal treatment of severe progressive Mooren’s ulcer, we here report on a retrospective case series of patients treated with systemic immunosuppressive therapy and additional amniotic membrane transplantation. METHODS: Medical records from seven patients (eleven eyes), 4 male and 3 female, with severe progressive Mooren’s ulcer were analysed retrospectively. The mean follow up was 88.4 ± 80.8 months (range 12–232 month). A HLA-typing was performed in all patients. A systemic immunosuppressive therapy was administered in all patients. The amniotic membrane was transplanted after the base of the ulcer was resected. RESULTS: Multiple amniotic membrane transplantations were necessary in six patients. The visual outcome of all patients was poor. No patient achieved a visual acuity better than 20/630 Snellen chart. Five patients were positive for HLA-DQ2 and four patients were positive for HLA-DR17(3). CONCLUSIONS: The aggressive and highly inflammatory form of Mooren’s ulcer is difficult to treat and the progression of the disease is hard to influence positively even under systemic immunosuppressive therapy. Therefore, the main intention of therapy is to achieve a stable epithelialized corneal surface without the risk of perforation. Amniotic membrane transplantation is not able to cure severe forms of Mooren’s ulcer. However it supports the immunosuppressive therapy in acute situations as in critical corneal thinning.
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spelling pubmed-38784112014-01-03 Amniotic membrane transplantation ineffective as additional therapy in patients with aggressive Mooren’s ulcer Schallenberg, Maurice Westekemper, Henrike Steuhl, Klaus-Peter Meller, Daniel BMC Ophthalmol Research Article BACKGROUND: Mooren’s ulcer is a severe ulcerative inflammation of the cornea. The exact pathogenesis remains unclear. Therefore many therapies of Mooren’s ulcer are recommended in literature. To shed more light on the ongoing question of optimal treatment of severe progressive Mooren’s ulcer, we here report on a retrospective case series of patients treated with systemic immunosuppressive therapy and additional amniotic membrane transplantation. METHODS: Medical records from seven patients (eleven eyes), 4 male and 3 female, with severe progressive Mooren’s ulcer were analysed retrospectively. The mean follow up was 88.4 ± 80.8 months (range 12–232 month). A HLA-typing was performed in all patients. A systemic immunosuppressive therapy was administered in all patients. The amniotic membrane was transplanted after the base of the ulcer was resected. RESULTS: Multiple amniotic membrane transplantations were necessary in six patients. The visual outcome of all patients was poor. No patient achieved a visual acuity better than 20/630 Snellen chart. Five patients were positive for HLA-DQ2 and four patients were positive for HLA-DR17(3). CONCLUSIONS: The aggressive and highly inflammatory form of Mooren’s ulcer is difficult to treat and the progression of the disease is hard to influence positively even under systemic immunosuppressive therapy. Therefore, the main intention of therapy is to achieve a stable epithelialized corneal surface without the risk of perforation. Amniotic membrane transplantation is not able to cure severe forms of Mooren’s ulcer. However it supports the immunosuppressive therapy in acute situations as in critical corneal thinning. BioMed Central 2013-12-17 /pmc/articles/PMC3878411/ /pubmed/24345289 http://dx.doi.org/10.1186/1471-2415-13-81 Text en Copyright © 2013 Schallenberg et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Schallenberg, Maurice
Westekemper, Henrike
Steuhl, Klaus-Peter
Meller, Daniel
Amniotic membrane transplantation ineffective as additional therapy in patients with aggressive Mooren’s ulcer
title Amniotic membrane transplantation ineffective as additional therapy in patients with aggressive Mooren’s ulcer
title_full Amniotic membrane transplantation ineffective as additional therapy in patients with aggressive Mooren’s ulcer
title_fullStr Amniotic membrane transplantation ineffective as additional therapy in patients with aggressive Mooren’s ulcer
title_full_unstemmed Amniotic membrane transplantation ineffective as additional therapy in patients with aggressive Mooren’s ulcer
title_short Amniotic membrane transplantation ineffective as additional therapy in patients with aggressive Mooren’s ulcer
title_sort amniotic membrane transplantation ineffective as additional therapy in patients with aggressive mooren’s ulcer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3878411/
https://www.ncbi.nlm.nih.gov/pubmed/24345289
http://dx.doi.org/10.1186/1471-2415-13-81
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