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Aberrant Corneal Homeostasis in Neurosurgery-Induced Neurotrophic Keratopathy

The characteristic features of neurotrophic keratopathy have been well documented by in vivo and in vitro studies using animal models. However, case reports of neurotrophic keratopathy induced by neurosurgery are limited. We describe the clinical characteristics, anterior segment optical coherence t...

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Autores principales: Oba, Shimpei, Araki-Sasaki, Kaoru, Chihara, Tomoyuki, Kojima, Takashi, Murat, Dogru, Takahashi, Kanji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267273/
https://www.ncbi.nlm.nih.gov/pubmed/35807085
http://dx.doi.org/10.3390/jcm11133804
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author Oba, Shimpei
Araki-Sasaki, Kaoru
Chihara, Tomoyuki
Kojima, Takashi
Murat, Dogru
Takahashi, Kanji
author_facet Oba, Shimpei
Araki-Sasaki, Kaoru
Chihara, Tomoyuki
Kojima, Takashi
Murat, Dogru
Takahashi, Kanji
author_sort Oba, Shimpei
collection PubMed
description The characteristic features of neurotrophic keratopathy have been well documented by in vivo and in vitro studies using animal models. However, case reports of neurotrophic keratopathy induced by neurosurgery are limited. We describe the clinical characteristics, anterior segment optical coherence tomography (AS-OCT) and in vivo confocal microscopy (IVCM) findings of neurotrophic keratopathy induced by surgery for intracranial lesions. This is a case series including 6 eyes of 3 patients (mean age, 69.67 ± 12.50 years) with unilateral neurotrophic keratopathy. The clinical findings of three patients were described and IVCM findings of three patients were analyzed. The duration of neuropathy ranged from 2 to 30 years (median, 22 years). Thickening of the epithelial layer and higher reflection density of the anterior stroma were observed during the healing process using AS-OCT. The mean nerve fiber density of the subepithelial plexus, as determined by IVCM, was 1943 ± 1000 μm/mm(2) for neurotrophic eyes and 2242 ± 600.3 μm/mm(2) for contralateral eyes (p = 0.0347). The mean respective dendritic cell densities were 30.8 ± 21.8 and 6.25 ± 5.59 cells/mm(2) (p < 0.0001), while the mean basal cell sizes were 259 ± 86.5 and 185 ± 45.9 μm(2) (p < 0.0001), respectively. These findings suggest that neurosurgery-induced neurotrophic keratopathy may be associated with alterations in the healing process and immune cell distribution in the cornea.
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spelling pubmed-92672732022-07-09 Aberrant Corneal Homeostasis in Neurosurgery-Induced Neurotrophic Keratopathy Oba, Shimpei Araki-Sasaki, Kaoru Chihara, Tomoyuki Kojima, Takashi Murat, Dogru Takahashi, Kanji J Clin Med Article The characteristic features of neurotrophic keratopathy have been well documented by in vivo and in vitro studies using animal models. However, case reports of neurotrophic keratopathy induced by neurosurgery are limited. We describe the clinical characteristics, anterior segment optical coherence tomography (AS-OCT) and in vivo confocal microscopy (IVCM) findings of neurotrophic keratopathy induced by surgery for intracranial lesions. This is a case series including 6 eyes of 3 patients (mean age, 69.67 ± 12.50 years) with unilateral neurotrophic keratopathy. The clinical findings of three patients were described and IVCM findings of three patients were analyzed. The duration of neuropathy ranged from 2 to 30 years (median, 22 years). Thickening of the epithelial layer and higher reflection density of the anterior stroma were observed during the healing process using AS-OCT. The mean nerve fiber density of the subepithelial plexus, as determined by IVCM, was 1943 ± 1000 μm/mm(2) for neurotrophic eyes and 2242 ± 600.3 μm/mm(2) for contralateral eyes (p = 0.0347). The mean respective dendritic cell densities were 30.8 ± 21.8 and 6.25 ± 5.59 cells/mm(2) (p < 0.0001), while the mean basal cell sizes were 259 ± 86.5 and 185 ± 45.9 μm(2) (p < 0.0001), respectively. These findings suggest that neurosurgery-induced neurotrophic keratopathy may be associated with alterations in the healing process and immune cell distribution in the cornea. MDPI 2022-06-30 /pmc/articles/PMC9267273/ /pubmed/35807085 http://dx.doi.org/10.3390/jcm11133804 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Oba, Shimpei
Araki-Sasaki, Kaoru
Chihara, Tomoyuki
Kojima, Takashi
Murat, Dogru
Takahashi, Kanji
Aberrant Corneal Homeostasis in Neurosurgery-Induced Neurotrophic Keratopathy
title Aberrant Corneal Homeostasis in Neurosurgery-Induced Neurotrophic Keratopathy
title_full Aberrant Corneal Homeostasis in Neurosurgery-Induced Neurotrophic Keratopathy
title_fullStr Aberrant Corneal Homeostasis in Neurosurgery-Induced Neurotrophic Keratopathy
title_full_unstemmed Aberrant Corneal Homeostasis in Neurosurgery-Induced Neurotrophic Keratopathy
title_short Aberrant Corneal Homeostasis in Neurosurgery-Induced Neurotrophic Keratopathy
title_sort aberrant corneal homeostasis in neurosurgery-induced neurotrophic keratopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9267273/
https://www.ncbi.nlm.nih.gov/pubmed/35807085
http://dx.doi.org/10.3390/jcm11133804
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