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Cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: A case report

PURPOSE: Cerebrospinal fluid hypovolemia syndrome (CHS) is a rare clinical entity that can be caused by spontaneous cerebrospinal fluid (CSF) leakage. The aim of this study is to report a rare case of CHS after a traffic accident in a patient who presented with diplopia and ptosis with fluctuation a...

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Autores principales: Shinkai, Akihiro, Shinmei, Yasuhiro, Takahashi, Akihiro, Nakamura, Kayoko, Tagawa, Yoshiaki, Chin, Shinki, Ishida, Susumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933691/
https://www.ncbi.nlm.nih.gov/pubmed/35313471
http://dx.doi.org/10.1016/j.ajoc.2022.101478
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author Shinkai, Akihiro
Shinmei, Yasuhiro
Takahashi, Akihiro
Nakamura, Kayoko
Tagawa, Yoshiaki
Chin, Shinki
Ishida, Susumu
author_facet Shinkai, Akihiro
Shinmei, Yasuhiro
Takahashi, Akihiro
Nakamura, Kayoko
Tagawa, Yoshiaki
Chin, Shinki
Ishida, Susumu
author_sort Shinkai, Akihiro
collection PubMed
description PURPOSE: Cerebrospinal fluid hypovolemia syndrome (CHS) is a rare clinical entity that can be caused by spontaneous cerebrospinal fluid (CSF) leakage. The aim of this study is to report a rare case of CHS after a traffic accident in a patient who presented with diplopia and ptosis with fluctuation and was initially diagnosed with ocular myasthenia gravis. OBSERVEATIONS: A 29-year-old man exhibited fluctuating left ptosis and diplopia after a traffic accident. Although he was suspected of having myasthenia gravis and was treated using oral pyridostigmine bromide, his symptoms did not improve. He also had orthostatic headaches and malaise after the accident. His symptoms were suspected to be associated with traumatic cerebrospinal fluid hypovolemia. After 1000-mL fluid replacement, his diplopia and ptosis improved, and orbital T2-weghted MRI detected a high-signal zone around the optic nerve. We diagnosed him with oculomotor nerve paresis associated with cerebrospinal fluid hypovolemia. The symptoms, including ptosis, diplopia, orthostatic headaches, and malaise, disappeared after epidural blood patch therapy. CONCLUSIONS AND IMPORTANCE: When treating patients with fluctuating ocular symptoms, such as diplopia and ptosis, who have a history of trauma and orthostatic headaches, the possibility of CHS should be considered in the differential diagnosis.
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spelling pubmed-89336912022-03-20 Cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: A case report Shinkai, Akihiro Shinmei, Yasuhiro Takahashi, Akihiro Nakamura, Kayoko Tagawa, Yoshiaki Chin, Shinki Ishida, Susumu Am J Ophthalmol Case Rep Case Report PURPOSE: Cerebrospinal fluid hypovolemia syndrome (CHS) is a rare clinical entity that can be caused by spontaneous cerebrospinal fluid (CSF) leakage. The aim of this study is to report a rare case of CHS after a traffic accident in a patient who presented with diplopia and ptosis with fluctuation and was initially diagnosed with ocular myasthenia gravis. OBSERVEATIONS: A 29-year-old man exhibited fluctuating left ptosis and diplopia after a traffic accident. Although he was suspected of having myasthenia gravis and was treated using oral pyridostigmine bromide, his symptoms did not improve. He also had orthostatic headaches and malaise after the accident. His symptoms were suspected to be associated with traumatic cerebrospinal fluid hypovolemia. After 1000-mL fluid replacement, his diplopia and ptosis improved, and orbital T2-weghted MRI detected a high-signal zone around the optic nerve. We diagnosed him with oculomotor nerve paresis associated with cerebrospinal fluid hypovolemia. The symptoms, including ptosis, diplopia, orthostatic headaches, and malaise, disappeared after epidural blood patch therapy. CONCLUSIONS AND IMPORTANCE: When treating patients with fluctuating ocular symptoms, such as diplopia and ptosis, who have a history of trauma and orthostatic headaches, the possibility of CHS should be considered in the differential diagnosis. Elsevier 2022-03-15 /pmc/articles/PMC8933691/ /pubmed/35313471 http://dx.doi.org/10.1016/j.ajoc.2022.101478 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
Shinkai, Akihiro
Shinmei, Yasuhiro
Takahashi, Akihiro
Nakamura, Kayoko
Tagawa, Yoshiaki
Chin, Shinki
Ishida, Susumu
Cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: A case report
title Cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: A case report
title_full Cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: A case report
title_fullStr Cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: A case report
title_full_unstemmed Cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: A case report
title_short Cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: A case report
title_sort cerebrospinal fluid hypovolemia syndrome mimicking ocular myasthenia gravis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933691/
https://www.ncbi.nlm.nih.gov/pubmed/35313471
http://dx.doi.org/10.1016/j.ajoc.2022.101478
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