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Fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy
PURPOSE: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a disease characterized by multiple yellowish-white placoid lesions. Although most lesions resolve spontaneously, some turn into scars and lead to permanent visual dysfunction. In this report, we found suggestive findings...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614854/ https://www.ncbi.nlm.nih.gov/pubmed/36312789 http://dx.doi.org/10.1016/j.ajoc.2022.101732 |
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author | Yokoi, Koichi Namba, Kenichi Iwata, Daiju Mizuuchi, Kazuomi Hase, Keitaro Suzuki, Kayo Ando, Ryo Hirooka, Kiriko Sekine, Nobuko Kitaichi, Nobuyoshi Hiraoka, Miki Ishida, Susumu |
author_facet | Yokoi, Koichi Namba, Kenichi Iwata, Daiju Mizuuchi, Kazuomi Hase, Keitaro Suzuki, Kayo Ando, Ryo Hirooka, Kiriko Sekine, Nobuko Kitaichi, Nobuyoshi Hiraoka, Miki Ishida, Susumu |
author_sort | Yokoi, Koichi |
collection | PubMed |
description | PURPOSE: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a disease characterized by multiple yellowish-white placoid lesions. Although most lesions resolve spontaneously, some turn into scars and lead to permanent visual dysfunction. In this report, we found suggestive findings in fundus autofluorescence (FAF) that may be useful for distinguishing severe lesions requiring treatment in APMPPE. OBSERVATION: Case 1: A 29-year-old woman was referred to our hospital with multiple yellowish-white placoid lesions on the fundi of both eyes (OU). FAF showed hyperautofluorescence in some of these placoid lesions. Based on the findings of fluorescein angiography, a diagnosis of APMPPE was established, and oral prednisolone (PSL) was initiated, given that some lesions were located in the macula. One week later, exacerbation occurred with the newly developed hyperautofluorescent lesions. Some lesions in the right eye (OD) that were hyperautofluorescent at the first visit became hypoautofluorescent. Afterward, although all hypoautofluorescent lesions persisted, most of the hyperautofluorescent lesions disappeared, so oral PSL could be stopped. Two months later, however, the recurrence occurred along with multiple new placoid lesions. Some lesions located at the macula were hyperautofluorescent on FAF OU, indicating the possibility of becoming scar lesions with hypoautofluorescence. Accordingly, oral PSL was given again. CASE 2: A 47-year-old woman noticed decreased vision OD, and she was referred to us. Multiple yellowish-white placoid lesions were seen in the fundi OU. FAF showed hyperautofluorescence both with and without corresponding hypoautofluorescence in the placoid lesions OU. A diagnosis of APMPPE was established, and oral PSL was initiated. Four months later, some lesions that were hyperautofluorescent at the first visit had turned isoautofluorescent, and some lesions OU became hypoautofluorescent. However, all hypoautofluorescent lesions remained hypoautofluorescent OU. Only some hyperautofluorescent lesions recovered to isoautofluorescence without scars. CONCLUSIONS AND IMPORTANCE: In APMPPE, lesions showing hyperautofluorescence on FAF may change into hypoautofluorescence indicating scar formation. Therefore, the presence of hyperautofluorescent lesions in the macula may be a good indicator of the need for intensive corticosteroid treatments to avoid leaving hypoautofluorescent scars that are related to irreversible visual dysfunction. |
format | Online Article Text |
id | pubmed-9614854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-96148542022-10-29 Fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy Yokoi, Koichi Namba, Kenichi Iwata, Daiju Mizuuchi, Kazuomi Hase, Keitaro Suzuki, Kayo Ando, Ryo Hirooka, Kiriko Sekine, Nobuko Kitaichi, Nobuyoshi Hiraoka, Miki Ishida, Susumu Am J Ophthalmol Case Rep Case Report PURPOSE: Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a disease characterized by multiple yellowish-white placoid lesions. Although most lesions resolve spontaneously, some turn into scars and lead to permanent visual dysfunction. In this report, we found suggestive findings in fundus autofluorescence (FAF) that may be useful for distinguishing severe lesions requiring treatment in APMPPE. OBSERVATION: Case 1: A 29-year-old woman was referred to our hospital with multiple yellowish-white placoid lesions on the fundi of both eyes (OU). FAF showed hyperautofluorescence in some of these placoid lesions. Based on the findings of fluorescein angiography, a diagnosis of APMPPE was established, and oral prednisolone (PSL) was initiated, given that some lesions were located in the macula. One week later, exacerbation occurred with the newly developed hyperautofluorescent lesions. Some lesions in the right eye (OD) that were hyperautofluorescent at the first visit became hypoautofluorescent. Afterward, although all hypoautofluorescent lesions persisted, most of the hyperautofluorescent lesions disappeared, so oral PSL could be stopped. Two months later, however, the recurrence occurred along with multiple new placoid lesions. Some lesions located at the macula were hyperautofluorescent on FAF OU, indicating the possibility of becoming scar lesions with hypoautofluorescence. Accordingly, oral PSL was given again. CASE 2: A 47-year-old woman noticed decreased vision OD, and she was referred to us. Multiple yellowish-white placoid lesions were seen in the fundi OU. FAF showed hyperautofluorescence both with and without corresponding hypoautofluorescence in the placoid lesions OU. A diagnosis of APMPPE was established, and oral PSL was initiated. Four months later, some lesions that were hyperautofluorescent at the first visit had turned isoautofluorescent, and some lesions OU became hypoautofluorescent. However, all hypoautofluorescent lesions remained hypoautofluorescent OU. Only some hyperautofluorescent lesions recovered to isoautofluorescence without scars. CONCLUSIONS AND IMPORTANCE: In APMPPE, lesions showing hyperautofluorescence on FAF may change into hypoautofluorescence indicating scar formation. Therefore, the presence of hyperautofluorescent lesions in the macula may be a good indicator of the need for intensive corticosteroid treatments to avoid leaving hypoautofluorescent scars that are related to irreversible visual dysfunction. Elsevier 2022-10-23 /pmc/articles/PMC9614854/ /pubmed/36312789 http://dx.doi.org/10.1016/j.ajoc.2022.101732 Text en © 2022 The Authors 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 Yokoi, Koichi Namba, Kenichi Iwata, Daiju Mizuuchi, Kazuomi Hase, Keitaro Suzuki, Kayo Ando, Ryo Hirooka, Kiriko Sekine, Nobuko Kitaichi, Nobuyoshi Hiraoka, Miki Ishida, Susumu Fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy |
title | Fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy |
title_full | Fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy |
title_fullStr | Fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy |
title_full_unstemmed | Fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy |
title_short | Fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy |
title_sort | fundus autofluorescence imaging in acute posterior multifocal placoid pigment epitheliopathy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614854/ https://www.ncbi.nlm.nih.gov/pubmed/36312789 http://dx.doi.org/10.1016/j.ajoc.2022.101732 |
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