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Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome

Satoyoshi syndrome is a rare systemic autoimmune disease that presents with painful muscle spasms. We report a case of impending central retinal vein occlusion (CRVO) secondary to granulomatous pan-uveitis in a 32-year-old woman with Satoyoshi syndrome. PATIENT CONCERNS: At the age of 7 years, she d...

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Autores principales: Saima, Yoshinari, Tanaka, Yoshiaki, Kakehashi, Akihiro, Kaburaki, Toshikatsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019272/
https://www.ncbi.nlm.nih.gov/pubmed/36930111
http://dx.doi.org/10.1097/MD.0000000000033284
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author Saima, Yoshinari
Tanaka, Yoshiaki
Kakehashi, Akihiro
Kaburaki, Toshikatsu
author_facet Saima, Yoshinari
Tanaka, Yoshiaki
Kakehashi, Akihiro
Kaburaki, Toshikatsu
author_sort Saima, Yoshinari
collection PubMed
description Satoyoshi syndrome is a rare systemic autoimmune disease that presents with painful muscle spasms. We report a case of impending central retinal vein occlusion (CRVO) secondary to granulomatous pan-uveitis in a 32-year-old woman with Satoyoshi syndrome. PATIENT CONCERNS: At the age of 7 years, she developed generalized hair loss and painful spasms and was diagnosed with Satoyoshi syndrome. Her current symptoms included sudden metamorphopsia and decreased visual acuity in the left eye. She visited our hospital with extensive intraretinal hemorrhage (including the macula), meandering of the retinal veins, and swelling of the optic disc. Fluorescence fundus angiography demonstrated hyper fluorescence of the optic disc and leakage from the retinal veins, suggesting CRVO associated with optic papillitis and segmental periphlebitis. DIAGNOSES: In the left eye, there were 2 + cells in the anterior chamber and 1 + in the anterior vitreous. INTERVENTIONS: We increased the existing dose of prednisolone for the treatment of uveitis and started her on oral aspirin and kallidinogenase for CRVO. OUTCOMES: The impending CRVO gradually subsided, and her visual acuity improved. However, during the subsequent treatment course, angle nodules were observed in the left eye, and the intraocular pressure (IOP) gradually increased. Although the angled nodules disappeared with topical corticosteroid treatment, the IOP did not reduce and became uncontrolled. Therefore, we performed trabeculotomy first, followed by trabeculectomy, after which the IOP decreased to approximately 10 mm Hg. LESSONS: Unilateral granulomatous pan-uveitis and impending CRVO were observed in this patient. Several cases of Satoyoshi syndrome complicated by various autoimmune or immunological disorders have been reported. However, to the best of our knowledge, no reports of Satoyoshi syndrome presenting with uveitis or CRVO have been published. Physicians should consider uveitis as a complication of Satoyoshi syndrome.
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spelling pubmed-100192722023-03-17 Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome Saima, Yoshinari Tanaka, Yoshiaki Kakehashi, Akihiro Kaburaki, Toshikatsu Medicine (Baltimore) 5800 Satoyoshi syndrome is a rare systemic autoimmune disease that presents with painful muscle spasms. We report a case of impending central retinal vein occlusion (CRVO) secondary to granulomatous pan-uveitis in a 32-year-old woman with Satoyoshi syndrome. PATIENT CONCERNS: At the age of 7 years, she developed generalized hair loss and painful spasms and was diagnosed with Satoyoshi syndrome. Her current symptoms included sudden metamorphopsia and decreased visual acuity in the left eye. She visited our hospital with extensive intraretinal hemorrhage (including the macula), meandering of the retinal veins, and swelling of the optic disc. Fluorescence fundus angiography demonstrated hyper fluorescence of the optic disc and leakage from the retinal veins, suggesting CRVO associated with optic papillitis and segmental periphlebitis. DIAGNOSES: In the left eye, there were 2 + cells in the anterior chamber and 1 + in the anterior vitreous. INTERVENTIONS: We increased the existing dose of prednisolone for the treatment of uveitis and started her on oral aspirin and kallidinogenase for CRVO. OUTCOMES: The impending CRVO gradually subsided, and her visual acuity improved. However, during the subsequent treatment course, angle nodules were observed in the left eye, and the intraocular pressure (IOP) gradually increased. Although the angled nodules disappeared with topical corticosteroid treatment, the IOP did not reduce and became uncontrolled. Therefore, we performed trabeculotomy first, followed by trabeculectomy, after which the IOP decreased to approximately 10 mm Hg. LESSONS: Unilateral granulomatous pan-uveitis and impending CRVO were observed in this patient. Several cases of Satoyoshi syndrome complicated by various autoimmune or immunological disorders have been reported. However, to the best of our knowledge, no reports of Satoyoshi syndrome presenting with uveitis or CRVO have been published. Physicians should consider uveitis as a complication of Satoyoshi syndrome. Lippincott Williams & Wilkins 2023-03-17 /pmc/articles/PMC10019272/ /pubmed/36930111 http://dx.doi.org/10.1097/MD.0000000000033284 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 5800
Saima, Yoshinari
Tanaka, Yoshiaki
Kakehashi, Akihiro
Kaburaki, Toshikatsu
Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
title Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
title_full Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
title_fullStr Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
title_full_unstemmed Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
title_short Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
title_sort impending central retinal vein occlusion and granulomatous uveitis in a patient with satoyoshi syndrome
topic 5800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10019272/
https://www.ncbi.nlm.nih.gov/pubmed/36930111
http://dx.doi.org/10.1097/MD.0000000000033284
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