Cargando…
Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge–Weber Syndrome
BACKGROUND: Sturge–Weber Syndrome (SWS) is a rare disease involving the eye, skin, and brain. Port-wine stain (PWS) and glaucoma are common clinical manifestations. This study analysed the clinical characteristics of infants with PWS and glaucoma secondary to SWS. METHODS: Children with PWS and glau...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185922/ https://www.ncbi.nlm.nih.gov/pubmed/35681114 http://dx.doi.org/10.1186/s12886-022-02476-x |
_version_ | 1784724824538480640 |
---|---|
author | Yan, Honggai Hu, Man Cui, Yanhui Li, Li Liang, Tianwei |
author_facet | Yan, Honggai Hu, Man Cui, Yanhui Li, Li Liang, Tianwei |
author_sort | Yan, Honggai |
collection | PubMed |
description | BACKGROUND: Sturge–Weber Syndrome (SWS) is a rare disease involving the eye, skin, and brain. Port-wine stain (PWS) and glaucoma are common clinical manifestations. This study analysed the clinical characteristics of infants with PWS and glaucoma secondary to SWS. METHODS: Children with PWS and glaucoma secondary to SWS were enrolled. Data were extracted from ophthalmic and systemic examination findings. Ocular examinations included intraocular pressure, anterior segment and fundus examination, and ocular A-scan and B-scan ultrasonography. RESULTS: Fifty-seven patients were included, with a mean age of 9.9 ± 11.9 months, and 34 (59.6%) patients were male. In all, 61 eyes were diagnosed with glaucoma. Forty-one patients (71.9%) had unilateral facial PWS and glaucoma occurred on the same side. Eight patients (14.0%) had Mongolian spots and ten patients (17.5%) had epilepsy. Corneal changes included corneal oedema (n = 36 eyes, 59.0%), corneal opacity (n = 15 eyes, 24.6%), and Haab lines (n = 13 eyes, 21.3%). Mean corneal diameter and thickness in the eyes with glaucoma was larger than those in the unaffected eyes (12.2 ± 0.7 mm vs 10.8 ± 0.6 mm, P < 0.001; 681.2 ± 106.4 µm vs 578.2 ± 58.2 µm, P < 0.001). The eyes with glaucoma had higher IOP and larger axial length and C/D ratio (19.3 ± 6.2 mmHg vs 11.6 ± 4.2 mmHg, P < 0.001; 21.23 ± 1.93 mm vs 19.68 ± 1.61 mm, P < 0.001; and 0.57 ± 0.18 vs 0.24 ± 0.15, P < 0.001). Thirty-three (57.9%) and 25 (43.9%) patients showed diffuse choroidal haemangioma (DCH) and conjunctival/episcleral haemangiomas, respectively. Ten patients (17.5%) showed iris anterior insertion or hyperpigmentation in the anterior chamber angles. Six of them had Mongolian spots at the same time. CONCLUSIONS: Monocular glaucoma, DCH, and conjunctival/episcleral haemangiomas are common in SWS patients with PWS and glaucoma. Glaucomatous eyes have larger corneal diameter and axial length and thicker cornea. Patients with Mongolian spots have higher incidence of iris anterior insertion or hyperpigmentation in anterior chamber angle. |
format | Online Article Text |
id | pubmed-9185922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91859222022-06-11 Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge–Weber Syndrome Yan, Honggai Hu, Man Cui, Yanhui Li, Li Liang, Tianwei BMC Ophthalmol Research BACKGROUND: Sturge–Weber Syndrome (SWS) is a rare disease involving the eye, skin, and brain. Port-wine stain (PWS) and glaucoma are common clinical manifestations. This study analysed the clinical characteristics of infants with PWS and glaucoma secondary to SWS. METHODS: Children with PWS and glaucoma secondary to SWS were enrolled. Data were extracted from ophthalmic and systemic examination findings. Ocular examinations included intraocular pressure, anterior segment and fundus examination, and ocular A-scan and B-scan ultrasonography. RESULTS: Fifty-seven patients were included, with a mean age of 9.9 ± 11.9 months, and 34 (59.6%) patients were male. In all, 61 eyes were diagnosed with glaucoma. Forty-one patients (71.9%) had unilateral facial PWS and glaucoma occurred on the same side. Eight patients (14.0%) had Mongolian spots and ten patients (17.5%) had epilepsy. Corneal changes included corneal oedema (n = 36 eyes, 59.0%), corneal opacity (n = 15 eyes, 24.6%), and Haab lines (n = 13 eyes, 21.3%). Mean corneal diameter and thickness in the eyes with glaucoma was larger than those in the unaffected eyes (12.2 ± 0.7 mm vs 10.8 ± 0.6 mm, P < 0.001; 681.2 ± 106.4 µm vs 578.2 ± 58.2 µm, P < 0.001). The eyes with glaucoma had higher IOP and larger axial length and C/D ratio (19.3 ± 6.2 mmHg vs 11.6 ± 4.2 mmHg, P < 0.001; 21.23 ± 1.93 mm vs 19.68 ± 1.61 mm, P < 0.001; and 0.57 ± 0.18 vs 0.24 ± 0.15, P < 0.001). Thirty-three (57.9%) and 25 (43.9%) patients showed diffuse choroidal haemangioma (DCH) and conjunctival/episcleral haemangiomas, respectively. Ten patients (17.5%) showed iris anterior insertion or hyperpigmentation in the anterior chamber angles. Six of them had Mongolian spots at the same time. CONCLUSIONS: Monocular glaucoma, DCH, and conjunctival/episcleral haemangiomas are common in SWS patients with PWS and glaucoma. Glaucomatous eyes have larger corneal diameter and axial length and thicker cornea. Patients with Mongolian spots have higher incidence of iris anterior insertion or hyperpigmentation in anterior chamber angle. BioMed Central 2022-06-09 /pmc/articles/PMC9185922/ /pubmed/35681114 http://dx.doi.org/10.1186/s12886-022-02476-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yan, Honggai Hu, Man Cui, Yanhui Li, Li Liang, Tianwei Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge–Weber Syndrome |
title | Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge–Weber Syndrome |
title_full | Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge–Weber Syndrome |
title_fullStr | Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge–Weber Syndrome |
title_full_unstemmed | Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge–Weber Syndrome |
title_short | Clinical characteristics of infants with port-wine stain and glaucoma secondary to Sturge–Weber Syndrome |
title_sort | clinical characteristics of infants with port-wine stain and glaucoma secondary to sturge–weber syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185922/ https://www.ncbi.nlm.nih.gov/pubmed/35681114 http://dx.doi.org/10.1186/s12886-022-02476-x |
work_keys_str_mv | AT yanhonggai clinicalcharacteristicsofinfantswithportwinestainandglaucomasecondarytosturgewebersyndrome AT human clinicalcharacteristicsofinfantswithportwinestainandglaucomasecondarytosturgewebersyndrome AT cuiyanhui clinicalcharacteristicsofinfantswithportwinestainandglaucomasecondarytosturgewebersyndrome AT lili clinicalcharacteristicsofinfantswithportwinestainandglaucomasecondarytosturgewebersyndrome AT liangtianwei clinicalcharacteristicsofinfantswithportwinestainandglaucomasecondarytosturgewebersyndrome |