Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1784671710959632384 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8933691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT shinkaiakihiro cerebrospinalfluidhypovolemiasyndromemimickingocularmyastheniagravisacasereport AT shinmeiyasuhiro cerebrospinalfluidhypovolemiasyndromemimickingocularmyastheniagravisacasereport AT takahashiakihiro cerebrospinalfluidhypovolemiasyndromemimickingocularmyastheniagravisacasereport AT nakamurakayoko cerebrospinalfluidhypovolemiasyndromemimickingocularmyastheniagravisacasereport AT tagawayoshiaki cerebrospinalfluidhypovolemiasyndromemimickingocularmyastheniagravisacasereport AT chinshinki cerebrospinalfluidhypovolemiasyndromemimickingocularmyastheniagravisacasereport AT ishidasusumu cerebrospinalfluidhypovolemiasyndromemimickingocularmyastheniagravisacasereport |