Comment on Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. J. Clin. Med. 2023, 12, 2704
We read with interest the recent article by Killian et al. regarding the characteristics and treatment of brain vascular malformations (VMs) in children and adults with hereditary hemorrhagic telangiectasia (HHT) [...]
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Published in | Journal of clinical medicine Vol. 12; no. 22; p. 7179 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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MDPI AG
20.11.2023
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ISSN | 2077-0383 2077-0383 |
DOI | 10.3390/jcm12227179 |
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Abstract | We read with interest the recent article by Killian et al. regarding the characteristics and treatment of brain vascular malformations (VMs) in children and adults with hereditary hemorrhagic telangiectasia (HHT) [...] |
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AbstractList | We read with interest the recent article by Killian et al. regarding the characteristics and treatment of brain vascular malformations (VMs) in children and adults with hereditary hemorrhagic telangiectasia (HHT) [...]. We read with interest the recent article by Killian et al. regarding the characteristics and treatment of brain vascular malformations (VMs) in children and adults with hereditary hemorrhagic telangiectasia (HHT) [...].We read with interest the recent article by Killian et al. regarding the characteristics and treatment of brain vascular malformations (VMs) in children and adults with hereditary hemorrhagic telangiectasia (HHT) [...]. [...]the study reports an increased prevalence of intracranial hemorrhage (ICH) at presentation in HHT patients (up to 23.7% and 9.9% in children and adult populations, respectively). [...]the authors aimed to evaluate the characteristics of brain VMs in HHT patients without mentioning their types. [...]the authors presented the proportions of treated brain VMs within the ruptured (23/27, 85%) and unruptured (46/87, 52.9%) groups of patients, respectively, rather than presenting the proportions of ruptured (23/69, 33.3%) and unruptured (46/69, 66.7%) VMs among the treated patients. Conflicts of Interest The authors declare no conflict of interest. |
Author | Boccardi, Edoardo Dupuis-Girod, Sophie Shovlin, Claire L. Eker, Omer F. |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38002793$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.3390/jcm12072704 10.1186/s13023-020-01386-9 10.1007/s00701-017-3154-8 10.3171/jns.2000.92.5.0779 10.3174/ajnr.A4762 10.3174/ajnr.A4210 10.1227/NEU.0000000000001103 10.1161/STROKEAHA.114.007367 10.2176/nmc.50.62 10.1161/01.STR.32.4.877 |
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Copyright | 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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References_xml | – ident: ref_1 doi: 10.3390/jcm12072704 – volume: 15 start-page: 165 year: 2020 ident: ref_9 article-title: European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT) publication-title: Orphanet J. Rare Dis. doi: 10.1186/s13023-020-01386-9 – volume: 159 start-page: 1059 year: 2017 ident: ref_8 article-title: European consensus conference on unruptured brain AVMs treatment (Supported by EANS, ESMINT, EGKS, and SINCH) publication-title: Acta Neurochir. doi: 10.1007/s00701-017-3154-8 – volume: 92 start-page: 779 year: 2000 ident: ref_2 article-title: Bleeding risk of cerebrovascular malformations in hereditary hemorrhagic telangiectasia publication-title: J. Neurosurg. doi: 10.3171/jns.2000.92.5.0779 – volume: 37 start-page: 1479 year: 2016 ident: ref_5 article-title: Neurovascular Manifestations of Hereditary Hemorrhagic Telangiectasia: A Consecutive Series of 376 Patients during 15 Years publication-title: AJNR Am. J. Neuroradiol. doi: 10.3174/ajnr.A4762 – volume: 36 start-page: 863 year: 2015 ident: ref_4 article-title: Neurovascular manifestations in hereditary hemorrhagic telangiectasia: Imaging features and genotype-phenotype correlations publication-title: AJNR Am. J. Neuroradiol. doi: 10.3174/ajnr.A4210 – volume: 78 start-page: 684 year: 2016 ident: ref_7 article-title: Lower Risk of Intracranial Arteriovenous Malformation Hemorrhage in Patients with Hereditary Hemorrhagic Telangiectasia publication-title: Neurosurgery doi: 10.1227/NEU.0000000000001103 – volume: 46 start-page: 1362 year: 2015 ident: ref_6 article-title: Hemorrhage rates from brain arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia publication-title: Stroke doi: 10.1161/STROKEAHA.114.007367 – volume: 50 start-page: 62 year: 2010 ident: ref_10 article-title: Delayed radiation necrosis 7 years after gamma knife surgery for arteriovenous malformation--two case reports publication-title: Neurol. Med. Chir. doi: 10.2176/nmc.50.62 – volume: 32 start-page: 877 year: 2001 ident: ref_3 article-title: Cerebrovascular manifestations in 321 cases of hereditary hemorrhagic telangiectasia publication-title: Stroke doi: 10.1161/01.STR.32.4.877 |
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Title | Comment on Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. J. Clin. Med. 2023, 12, 2704 |
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