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Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes
This retrospective observational case series is to evaluate the histopathological findings of drooping eyelids in patients with infantile-onset Pompe disease and assess the feasibility of levator muscle resection combined with conjoint fascial sheath suspension for ptosis correction. It included six...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034147/ https://www.ncbi.nlm.nih.gov/pubmed/36967722 http://dx.doi.org/10.1016/j.ymgmr.2023.100969 |
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author | Chen, Yi-Hua Huang, Pei-Wei Liu, Yu-Jen Tsai, Yueh-Ju |
author_facet | Chen, Yi-Hua Huang, Pei-Wei Liu, Yu-Jen Tsai, Yueh-Ju |
author_sort | Chen, Yi-Hua |
collection | PubMed |
description | This retrospective observational case series is to evaluate the histopathological findings of drooping eyelids in patients with infantile-onset Pompe disease and assess the feasibility of levator muscle resection combined with conjoint fascial sheath suspension for ptosis correction. It included six patients from a single tertiary referral center with ptosis and infantile-onset Pompe disease between January 1, 2013, and December 31, 2021. They most suffered from recurrent ptosis after initial surgical correction (6/11 eyes, 54.55%). The recurrence rate was high in eyes with levator muscle resection alone (4/6 eyes, 66.67%). No recurrence of ptosis was observed in eyes with levator muscle resection combined with conjoint fascial sheath suspension. The follow-up period was approximately 16–94 months. Histopathological examination revealed that the levator muscle had the most abundant glycogen accumulation-related vacuolar changes, followed by Müller's muscle and extraocular muscles. No vacuolar changes were observed in the conjoint fascial sheath. For patients with infantile-onset Pompe disease-related ptosis, performing levator muscle resection alone is not sufficient, while utilizing conjoint fascial sheath suspension can achieve the desired long-term outcomes with minimal recurrence. These findings may have important implications for the management of ophthalmic complications in patients with infantile-onset Pompe disease. |
format | Online Article Text |
id | pubmed-10034147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-100341472023-03-24 Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes Chen, Yi-Hua Huang, Pei-Wei Liu, Yu-Jen Tsai, Yueh-Ju Mol Genet Metab Rep Case Report This retrospective observational case series is to evaluate the histopathological findings of drooping eyelids in patients with infantile-onset Pompe disease and assess the feasibility of levator muscle resection combined with conjoint fascial sheath suspension for ptosis correction. It included six patients from a single tertiary referral center with ptosis and infantile-onset Pompe disease between January 1, 2013, and December 31, 2021. They most suffered from recurrent ptosis after initial surgical correction (6/11 eyes, 54.55%). The recurrence rate was high in eyes with levator muscle resection alone (4/6 eyes, 66.67%). No recurrence of ptosis was observed in eyes with levator muscle resection combined with conjoint fascial sheath suspension. The follow-up period was approximately 16–94 months. Histopathological examination revealed that the levator muscle had the most abundant glycogen accumulation-related vacuolar changes, followed by Müller's muscle and extraocular muscles. No vacuolar changes were observed in the conjoint fascial sheath. For patients with infantile-onset Pompe disease-related ptosis, performing levator muscle resection alone is not sufficient, while utilizing conjoint fascial sheath suspension can achieve the desired long-term outcomes with minimal recurrence. These findings may have important implications for the management of ophthalmic complications in patients with infantile-onset Pompe disease. Elsevier 2023-03-17 /pmc/articles/PMC10034147/ /pubmed/36967722 http://dx.doi.org/10.1016/j.ymgmr.2023.100969 Text en © 2023 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Chen, Yi-Hua Huang, Pei-Wei Liu, Yu-Jen Tsai, Yueh-Ju Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes |
title | Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes |
title_full | Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes |
title_fullStr | Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes |
title_full_unstemmed | Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes |
title_short | Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes |
title_sort | blepharoptosis in infantile onset pompe disease: histological findings and surgical outcomes |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034147/ https://www.ncbi.nlm.nih.gov/pubmed/36967722 http://dx.doi.org/10.1016/j.ymgmr.2023.100969 |
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