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Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report
BACKGROUND: Primary familial brain calcification (PFBC), habitually called Fahr’s disease, is characterized by bilateral calcification of the basal ganglia, accompanied by extensive calcification of the cerebellar dentate nucleus, brainstem cerebrum, and cerebellum at the grey-white matter junction....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869586/ https://www.ncbi.nlm.nih.gov/pubmed/36690936 http://dx.doi.org/10.1186/s12883-023-03072-2 |
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author | Yu, Kuangyang Pang, Jinwei Yang, Xiaobo Peng, Jianhua Jiang, Yong |
author_facet | Yu, Kuangyang Pang, Jinwei Yang, Xiaobo Peng, Jianhua Jiang, Yong |
author_sort | Yu, Kuangyang |
collection | PubMed |
description | BACKGROUND: Primary familial brain calcification (PFBC), habitually called Fahr’s disease, is characterized by bilateral calcification of the basal ganglia, accompanied by extensive calcification of the cerebellar dentate nucleus, brainstem cerebrum, and cerebellum at the grey-white matter junction. However, there are few reports about PFBC with aneurysmal subarachnoid hemorrhage (aSAH) and thalassemia. CASE PRESENTATION: We describe a patient admitted to the hospital with an acute deterioration in the level of consciousness with no history of neuropsychiatric features or movement disorders. After computed tomography (CT) and CT angiography (CTA), the patient was diagnosed with PFBC, accompanied by aneurysmal subarachnoid haemorrhage (aSAH), intracranial haemorrhage (ICH), and hemoglobin electrophoresis suggested beta-thalassemia. This patient underwent craniotomy aneurysm clipping and intracranial hematoma removal. CONCLUSIONS: For patients with PFBC, we should pay attention to their blood pressure and intracranial vascular conditions. The CTA is necessary to clarify the cerebrovascular conditions of the patient, especially when combined with hypertension and persistent headache or other related prodromal symptoms of cerebrovascular disease. |
format | Online Article Text |
id | pubmed-9869586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98695862023-01-24 Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report Yu, Kuangyang Pang, Jinwei Yang, Xiaobo Peng, Jianhua Jiang, Yong BMC Neurol Case Report BACKGROUND: Primary familial brain calcification (PFBC), habitually called Fahr’s disease, is characterized by bilateral calcification of the basal ganglia, accompanied by extensive calcification of the cerebellar dentate nucleus, brainstem cerebrum, and cerebellum at the grey-white matter junction. However, there are few reports about PFBC with aneurysmal subarachnoid hemorrhage (aSAH) and thalassemia. CASE PRESENTATION: We describe a patient admitted to the hospital with an acute deterioration in the level of consciousness with no history of neuropsychiatric features or movement disorders. After computed tomography (CT) and CT angiography (CTA), the patient was diagnosed with PFBC, accompanied by aneurysmal subarachnoid haemorrhage (aSAH), intracranial haemorrhage (ICH), and hemoglobin electrophoresis suggested beta-thalassemia. This patient underwent craniotomy aneurysm clipping and intracranial hematoma removal. CONCLUSIONS: For patients with PFBC, we should pay attention to their blood pressure and intracranial vascular conditions. The CTA is necessary to clarify the cerebrovascular conditions of the patient, especially when combined with hypertension and persistent headache or other related prodromal symptoms of cerebrovascular disease. BioMed Central 2023-01-23 /pmc/articles/PMC9869586/ /pubmed/36690936 http://dx.doi.org/10.1186/s12883-023-03072-2 Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Yu, Kuangyang Pang, Jinwei Yang, Xiaobo Peng, Jianhua Jiang, Yong Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report |
title | Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report |
title_full | Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report |
title_fullStr | Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report |
title_full_unstemmed | Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report |
title_short | Aneurysmal subarachnoid hemorrhage with PFBC and beta thalassemia: a case report |
title_sort | aneurysmal subarachnoid hemorrhage with pfbc and beta thalassemia: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869586/ https://www.ncbi.nlm.nih.gov/pubmed/36690936 http://dx.doi.org/10.1186/s12883-023-03072-2 |
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