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The Acute Superficial Siderosis Syndrome — Clinical Entity, Imaging Findings, and Histopathology
Superficial siderosis is a consequence of repetitive bleeding into the subarachnoid space, leading to toxic iron and hemosiderin deposits on the surface of the brain and spine. The clinical and radiological phenotypes of superficial siderosis are known to manifest over long time intervals. In contra...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985565/ https://www.ncbi.nlm.nih.gov/pubmed/35316464 http://dx.doi.org/10.1007/s12311-022-01387-3 |
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author | Friedauer, Lucie Foerch, Christian Steinbach, Joachim Hattingen, Elke Harter, Patrick N. Armbrust, Moritz Urban, Hans Steidl, Eike Neuhaus, Elisabeth von Brauchitsch, Sophie |
author_facet | Friedauer, Lucie Foerch, Christian Steinbach, Joachim Hattingen, Elke Harter, Patrick N. Armbrust, Moritz Urban, Hans Steidl, Eike Neuhaus, Elisabeth von Brauchitsch, Sophie |
author_sort | Friedauer, Lucie |
collection | PubMed |
description | Superficial siderosis is a consequence of repetitive bleeding into the subarachnoid space, leading to toxic iron and hemosiderin deposits on the surface of the brain and spine. The clinical and radiological phenotypes of superficial siderosis are known to manifest over long time intervals. In contrast, this study defines the “acute superficial siderosis syndrome” and illustrates typical imaging and histopathological findings of this entity. We describe the case of a 61-year-old male patient who was diagnosed with a melanoma metastasis in the right frontal cortex in February 2019. Within a few weeks he developed a progressive syndrome characterized by cerebellar ataxia, gait disturbance, signs of myelopathy, and radiculopathy. MRI revealed ongoing hemorrhage from the metastasis into the lateral ventricle and the subarachnoid space. A semiquantitative assessment of three subsequent MRI within an 8-week period documented the rapid development of superficial siderosis along the surface of the cerebellum, the brain stem, and the lower parts of the supratentorial regions on T2*-weighted sequences. The diagnosis of a superficial siderosis was histopathologically confirmed by identifying iron and hemosiderin deposits on the cortex along with astrogliosis. The recognition of this “acute superficial siderosis syndrome” triggered surgical removal of the hemorrhagic metastasis. Based on a single case presentation, we define the “acute superficial siderosis syndrome” as a clinical entity and describe the radiological and histopathological characteristics of this entity. Early recognition of this syndrome may allow timely elimination of the bleeding source, in order to prevent further clinical deterioration. |
format | Online Article Text |
id | pubmed-9985565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-99855652023-03-06 The Acute Superficial Siderosis Syndrome — Clinical Entity, Imaging Findings, and Histopathology Friedauer, Lucie Foerch, Christian Steinbach, Joachim Hattingen, Elke Harter, Patrick N. Armbrust, Moritz Urban, Hans Steidl, Eike Neuhaus, Elisabeth von Brauchitsch, Sophie Cerebellum Original Article Superficial siderosis is a consequence of repetitive bleeding into the subarachnoid space, leading to toxic iron and hemosiderin deposits on the surface of the brain and spine. The clinical and radiological phenotypes of superficial siderosis are known to manifest over long time intervals. In contrast, this study defines the “acute superficial siderosis syndrome” and illustrates typical imaging and histopathological findings of this entity. We describe the case of a 61-year-old male patient who was diagnosed with a melanoma metastasis in the right frontal cortex in February 2019. Within a few weeks he developed a progressive syndrome characterized by cerebellar ataxia, gait disturbance, signs of myelopathy, and radiculopathy. MRI revealed ongoing hemorrhage from the metastasis into the lateral ventricle and the subarachnoid space. A semiquantitative assessment of three subsequent MRI within an 8-week period documented the rapid development of superficial siderosis along the surface of the cerebellum, the brain stem, and the lower parts of the supratentorial regions on T2*-weighted sequences. The diagnosis of a superficial siderosis was histopathologically confirmed by identifying iron and hemosiderin deposits on the cortex along with astrogliosis. The recognition of this “acute superficial siderosis syndrome” triggered surgical removal of the hemorrhagic metastasis. Based on a single case presentation, we define the “acute superficial siderosis syndrome” as a clinical entity and describe the radiological and histopathological characteristics of this entity. Early recognition of this syndrome may allow timely elimination of the bleeding source, in order to prevent further clinical deterioration. Springer US 2022-03-22 2023 /pmc/articles/PMC9985565/ /pubmed/35316464 http://dx.doi.org/10.1007/s12311-022-01387-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Friedauer, Lucie Foerch, Christian Steinbach, Joachim Hattingen, Elke Harter, Patrick N. Armbrust, Moritz Urban, Hans Steidl, Eike Neuhaus, Elisabeth von Brauchitsch, Sophie The Acute Superficial Siderosis Syndrome — Clinical Entity, Imaging Findings, and Histopathology |
title | The Acute Superficial Siderosis Syndrome — Clinical Entity, Imaging Findings, and Histopathology |
title_full | The Acute Superficial Siderosis Syndrome — Clinical Entity, Imaging Findings, and Histopathology |
title_fullStr | The Acute Superficial Siderosis Syndrome — Clinical Entity, Imaging Findings, and Histopathology |
title_full_unstemmed | The Acute Superficial Siderosis Syndrome — Clinical Entity, Imaging Findings, and Histopathology |
title_short | The Acute Superficial Siderosis Syndrome — Clinical Entity, Imaging Findings, and Histopathology |
title_sort | acute superficial siderosis syndrome — clinical entity, imaging findings, and histopathology |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985565/ https://www.ncbi.nlm.nih.gov/pubmed/35316464 http://dx.doi.org/10.1007/s12311-022-01387-3 |
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