Cargando…
A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss
PURPOSE: To report family members with familial retinal arteriolar tortuosity (FRAT) identified after sudden visual loss. OBSERVATIONS: A 15-year-old boy had sudden visual loss in his left eye while playing on a horizontal bar. He was referred to Nagoya City University Hospital from an eye clinic. T...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603015/ https://www.ncbi.nlm.nih.gov/pubmed/34825110 http://dx.doi.org/10.1016/j.ajoc.2021.101230 |
_version_ | 1784601686643310592 |
---|---|
author | Obayashi, Tomohiro Kato, Aki Suzuki, Harumitsu Ohashi, Kei Yoshida, Munenori Shibata, Yu Ogura, Yuichiro Yasukawa, Tsutomu |
author_facet | Obayashi, Tomohiro Kato, Aki Suzuki, Harumitsu Ohashi, Kei Yoshida, Munenori Shibata, Yu Ogura, Yuichiro Yasukawa, Tsutomu |
author_sort | Obayashi, Tomohiro |
collection | PubMed |
description | PURPOSE: To report family members with familial retinal arteriolar tortuosity (FRAT) identified after sudden visual loss. OBSERVATIONS: A 15-year-old boy had sudden visual loss in his left eye while playing on a horizontal bar. He was referred to Nagoya City University Hospital from an eye clinic. The ophthalmologic examination showed retinal hemorrhage bilaterally. His best-corrected visual acuity (BCVA) was 20/17 in the right eye and 20/67 in the left eye. Bilateral retinal arteriolar tortuosity as well as retinal hemorrhage was seen. Since his mother with 54 years of age also had a history of retinal hemorrhage that improved spontaneously, fundus examination was performed, revealing tortuosity of the retinal arterioles. Consequently, the patient and his mother were diagnosed as FRAT. He was followed without intervention. Retinal hemorrhage gradually decreased and resolved after 3 months. The BCVA of his left eye gradually improved and reached 20/20 after 1 year. CONCLUSIONS AND IMPORTANCE: In this case, the family history was very useful for early diagnosis. Immediate and accurate diagnosis allowed the patient to be followed without intervention and achieve subsequent resolution of retinal hemorrhage and improved vision. FRAT should be considered in cases of sub-internal limiting membrane hemorrhages in young patients even in the presence of discrete retinal arteriolar tortuosity. |
format | Online Article Text |
id | pubmed-8603015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86030152021-11-24 A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss Obayashi, Tomohiro Kato, Aki Suzuki, Harumitsu Ohashi, Kei Yoshida, Munenori Shibata, Yu Ogura, Yuichiro Yasukawa, Tsutomu Am J Ophthalmol Case Rep Case Report PURPOSE: To report family members with familial retinal arteriolar tortuosity (FRAT) identified after sudden visual loss. OBSERVATIONS: A 15-year-old boy had sudden visual loss in his left eye while playing on a horizontal bar. He was referred to Nagoya City University Hospital from an eye clinic. The ophthalmologic examination showed retinal hemorrhage bilaterally. His best-corrected visual acuity (BCVA) was 20/17 in the right eye and 20/67 in the left eye. Bilateral retinal arteriolar tortuosity as well as retinal hemorrhage was seen. Since his mother with 54 years of age also had a history of retinal hemorrhage that improved spontaneously, fundus examination was performed, revealing tortuosity of the retinal arterioles. Consequently, the patient and his mother were diagnosed as FRAT. He was followed without intervention. Retinal hemorrhage gradually decreased and resolved after 3 months. The BCVA of his left eye gradually improved and reached 20/20 after 1 year. CONCLUSIONS AND IMPORTANCE: In this case, the family history was very useful for early diagnosis. Immediate and accurate diagnosis allowed the patient to be followed without intervention and achieve subsequent resolution of retinal hemorrhage and improved vision. FRAT should be considered in cases of sub-internal limiting membrane hemorrhages in young patients even in the presence of discrete retinal arteriolar tortuosity. Elsevier 2021-11-09 /pmc/articles/PMC8603015/ /pubmed/34825110 http://dx.doi.org/10.1016/j.ajoc.2021.101230 Text en © 2021 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 Obayashi, Tomohiro Kato, Aki Suzuki, Harumitsu Ohashi, Kei Yoshida, Munenori Shibata, Yu Ogura, Yuichiro Yasukawa, Tsutomu A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss |
title | A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss |
title_full | A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss |
title_fullStr | A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss |
title_full_unstemmed | A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss |
title_short | A case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss |
title_sort | case series from a single family of familial retinal arteriolar tortuosity with common history of sudden visual loss |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603015/ https://www.ncbi.nlm.nih.gov/pubmed/34825110 http://dx.doi.org/10.1016/j.ajoc.2021.101230 |
work_keys_str_mv | AT obayashitomohiro acaseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT katoaki acaseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT suzukiharumitsu acaseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT ohashikei acaseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT yoshidamunenori acaseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT shibatayu acaseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT ogurayuichiro acaseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT yasukawatsutomu acaseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT obayashitomohiro caseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT katoaki caseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT suzukiharumitsu caseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT ohashikei caseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT yoshidamunenori caseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT shibatayu caseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT ogurayuichiro caseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss AT yasukawatsutomu caseseriesfromasinglefamilyoffamilialretinalarteriolartortuositywithcommonhistoryofsuddenvisualloss |