Cargando…
Idiopathic superficial siderosis of the central nervous system
BACKGROUND: Regardless of the cause of the superficial siderosis (SS) disease, which is bleeding, the source of bleeding cannot be found in some cases. CASE PRESENTATION: In this article, we report two cases with idiopathic SS. Case 1 presented with bilateral hearing loss, cognitive impairment, slee...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908722/ https://www.ncbi.nlm.nih.gov/pubmed/33632336 http://dx.doi.org/10.1186/s40673-021-00133-5 |
_version_ | 1783655777926381568 |
---|---|
author | Meshkat, Shakila Ebrahimi, Parnia Tafakhori, Abbas Taghiloo, Aidin Shafiee, Sajad Salimi, Amir Aghamollaii, Vajiheh |
author_facet | Meshkat, Shakila Ebrahimi, Parnia Tafakhori, Abbas Taghiloo, Aidin Shafiee, Sajad Salimi, Amir Aghamollaii, Vajiheh |
author_sort | Meshkat, Shakila |
collection | PubMed |
description | BACKGROUND: Regardless of the cause of the superficial siderosis (SS) disease, which is bleeding, the source of bleeding cannot be found in some cases. CASE PRESENTATION: In this article, we report two cases with idiopathic SS. Case 1 presented with bilateral hearing loss, cognitive impairment, sleep disturbances, and tremors. Case 2 presented with sensory neural hearing loss, ataxia, and spastic paraparesis. In both cases, brain MRI indicated evidence of SS. CT myelogram and SPECT with labeled RBC couldn’t help finding the source of occult bleeding. CONCLUSION: SS is a rare central nervous system disease caused by the deposition of hemosiderin in the brain and spinal cord, which results in the progression of neurological deficits. The cause of this hemorrhage is often subarachnoid haemorrhage, intracranial surgery, carcinoma, arteriovenous malformation, nerve root avulsion, and dural abnormality. The condition progresses slowly and, by the time diagnosis is confirmed, the damage is often irreversible. In our cases, brain MRI clarified the definitive diagnosis, but we could not find the source of bleeding. SS should be considered in cases with ataxia and hearing loss, even if no source of bleeding is found. |
format | Online Article Text |
id | pubmed-7908722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79087222021-03-02 Idiopathic superficial siderosis of the central nervous system Meshkat, Shakila Ebrahimi, Parnia Tafakhori, Abbas Taghiloo, Aidin Shafiee, Sajad Salimi, Amir Aghamollaii, Vajiheh Cerebellum Ataxias Case Report BACKGROUND: Regardless of the cause of the superficial siderosis (SS) disease, which is bleeding, the source of bleeding cannot be found in some cases. CASE PRESENTATION: In this article, we report two cases with idiopathic SS. Case 1 presented with bilateral hearing loss, cognitive impairment, sleep disturbances, and tremors. Case 2 presented with sensory neural hearing loss, ataxia, and spastic paraparesis. In both cases, brain MRI indicated evidence of SS. CT myelogram and SPECT with labeled RBC couldn’t help finding the source of occult bleeding. CONCLUSION: SS is a rare central nervous system disease caused by the deposition of hemosiderin in the brain and spinal cord, which results in the progression of neurological deficits. The cause of this hemorrhage is often subarachnoid haemorrhage, intracranial surgery, carcinoma, arteriovenous malformation, nerve root avulsion, and dural abnormality. The condition progresses slowly and, by the time diagnosis is confirmed, the damage is often irreversible. In our cases, brain MRI clarified the definitive diagnosis, but we could not find the source of bleeding. SS should be considered in cases with ataxia and hearing loss, even if no source of bleeding is found. BioMed Central 2021-02-25 /pmc/articles/PMC7908722/ /pubmed/33632336 http://dx.doi.org/10.1186/s40673-021-00133-5 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Meshkat, Shakila Ebrahimi, Parnia Tafakhori, Abbas Taghiloo, Aidin Shafiee, Sajad Salimi, Amir Aghamollaii, Vajiheh Idiopathic superficial siderosis of the central nervous system |
title | Idiopathic superficial siderosis of the central nervous system |
title_full | Idiopathic superficial siderosis of the central nervous system |
title_fullStr | Idiopathic superficial siderosis of the central nervous system |
title_full_unstemmed | Idiopathic superficial siderosis of the central nervous system |
title_short | Idiopathic superficial siderosis of the central nervous system |
title_sort | idiopathic superficial siderosis of the central nervous system |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908722/ https://www.ncbi.nlm.nih.gov/pubmed/33632336 http://dx.doi.org/10.1186/s40673-021-00133-5 |
work_keys_str_mv | AT meshkatshakila idiopathicsuperficialsiderosisofthecentralnervoussystem AT ebrahimiparnia idiopathicsuperficialsiderosisofthecentralnervoussystem AT tafakhoriabbas idiopathicsuperficialsiderosisofthecentralnervoussystem AT taghilooaidin idiopathicsuperficialsiderosisofthecentralnervoussystem AT shafieesajad idiopathicsuperficialsiderosisofthecentralnervoussystem AT salimiamir idiopathicsuperficialsiderosisofthecentralnervoussystem AT aghamollaiivajiheh idiopathicsuperficialsiderosisofthecentralnervoussystem |