Cargando…
Intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review
BACKGROUND: Inflammatory Myofibroblastoma Tumors (IMTs) are extremely tumour rare in the intraocular. CASE PRESENTATION: A ciliary body tumor was found under slit lamp biomicroscopy in a 55-year-old male first diagnosed with cataract. Then this patient underwent trans-sclera resection via partial la...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063157/ https://www.ncbi.nlm.nih.gov/pubmed/35501775 http://dx.doi.org/10.1186/s12886-022-02411-0 |
_version_ | 1784699106731491328 |
---|---|
author | Yu, He Zhang, Caixin Tong, Nianting Wang, Xiu Wang, Liangyu Gong, Huimin Liu, Xin Zhou, Zhanyu |
author_facet | Yu, He Zhang, Caixin Tong, Nianting Wang, Xiu Wang, Liangyu Gong, Huimin Liu, Xin Zhou, Zhanyu |
author_sort | Yu, He |
collection | PubMed |
description | BACKGROUND: Inflammatory Myofibroblastoma Tumors (IMTs) are extremely tumour rare in the intraocular. CASE PRESENTATION: A ciliary body tumor was found under slit lamp biomicroscopy in a 55-year-old male first diagnosed with cataract. Then this patient underwent trans-sclera resection via partial lamellar sclerouvectomy and par plans vitrectomy to remove the mass. Hematoxylin and eosin (HE) staining and immunohistochemistry findings showed that the characteristics of the tumor were consistent with IMT. CONCLUSIONS: We reported a rare case of intraocular IMT, which is confirmed by H&E staining, and IHC positive staining for Vimentin, Desmin and ALK, while negative staining for SMA, S-100, ki-67, CK, CD68, and calponin. |
format | Online Article Text |
id | pubmed-9063157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90631572022-05-04 Intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review Yu, He Zhang, Caixin Tong, Nianting Wang, Xiu Wang, Liangyu Gong, Huimin Liu, Xin Zhou, Zhanyu BMC Ophthalmol Case Report BACKGROUND: Inflammatory Myofibroblastoma Tumors (IMTs) are extremely tumour rare in the intraocular. CASE PRESENTATION: A ciliary body tumor was found under slit lamp biomicroscopy in a 55-year-old male first diagnosed with cataract. Then this patient underwent trans-sclera resection via partial lamellar sclerouvectomy and par plans vitrectomy to remove the mass. Hematoxylin and eosin (HE) staining and immunohistochemistry findings showed that the characteristics of the tumor were consistent with IMT. CONCLUSIONS: We reported a rare case of intraocular IMT, which is confirmed by H&E staining, and IHC positive staining for Vimentin, Desmin and ALK, while negative staining for SMA, S-100, ki-67, CK, CD68, and calponin. BioMed Central 2022-05-02 /pmc/articles/PMC9063157/ /pubmed/35501775 http://dx.doi.org/10.1186/s12886-022-02411-0 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 | Case Report Yu, He Zhang, Caixin Tong, Nianting Wang, Xiu Wang, Liangyu Gong, Huimin Liu, Xin Zhou, Zhanyu Intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review |
title | Intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review |
title_full | Intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review |
title_fullStr | Intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review |
title_full_unstemmed | Intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review |
title_short | Intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review |
title_sort | intraocular myofibroblastoma tumour of the ciliary body: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063157/ https://www.ncbi.nlm.nih.gov/pubmed/35501775 http://dx.doi.org/10.1186/s12886-022-02411-0 |
work_keys_str_mv | AT yuhe intraocularmyofibroblastomatumouroftheciliarybodyacasereportandliteraturereview AT zhangcaixin intraocularmyofibroblastomatumouroftheciliarybodyacasereportandliteraturereview AT tongnianting intraocularmyofibroblastomatumouroftheciliarybodyacasereportandliteraturereview AT wangxiu intraocularmyofibroblastomatumouroftheciliarybodyacasereportandliteraturereview AT wangliangyu intraocularmyofibroblastomatumouroftheciliarybodyacasereportandliteraturereview AT gonghuimin intraocularmyofibroblastomatumouroftheciliarybodyacasereportandliteraturereview AT liuxin intraocularmyofibroblastomatumouroftheciliarybodyacasereportandliteraturereview AT zhouzhanyu intraocularmyofibroblastomatumouroftheciliarybodyacasereportandliteraturereview |