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Hemangioblastoma with late leptomeningeal metastasis: a case report
BACKGROUND: Hemangioblastoma of the central nervous system is an uncommon benign neoplasm, with about 25% of cases in patients with von Hippel–Lindau disease. The incidence of metastasis is rare, particularly in patients without von Hippel–Lindau disease. We report a case of hemangioblastoma with le...
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/PMC10026473/ https://www.ncbi.nlm.nih.gov/pubmed/36935497 http://dx.doi.org/10.1186/s13256-023-03812-5 |
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author | Poiset, Spencer J. Reddy, Aneesh Tucker, Catherine M. Kenyon, Lawrence C. Judy, Kevin D. Shi, Wenyin |
author_facet | Poiset, Spencer J. Reddy, Aneesh Tucker, Catherine M. Kenyon, Lawrence C. Judy, Kevin D. Shi, Wenyin |
author_sort | Poiset, Spencer J. |
collection | PubMed |
description | BACKGROUND: Hemangioblastoma of the central nervous system is an uncommon benign neoplasm, with about 25% of cases in patients with von Hippel–Lindau disease. The incidence of metastasis is rare, particularly in patients without von Hippel–Lindau disease. We report a case of hemangioblastoma with leptomeningeal dissemination as a late recurrence. CASE PRESENTATION: A 65-year-old Caucasian man with a history of World Health Organization grade I hemangioblastoma of the cerebellar vermis underwent gross total resection in 1997. In early 2018, he developed intracranial recurrences with diffuse leptomeningeal disease of the entire spine. The patient underwent resection of intracranial recurrence, followed by palliative craniospinal irradiation. The disease progressed quickly, and he died 8 months after recurrence. CONCLUSIONS: Despite a benign pathology, hemangioblastoma has a low risk of metastasis. The outcome for hemangioblastoma patients with metastasis is poor. Multidisciplinary care for patients with metastatic hemangioblastoma warrants further investigation, and an effective systemic option is urgently needed. Regular lifelong follow-up of at-risk patients is recommended. |
format | Online Article Text |
id | pubmed-10026473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100264732023-03-21 Hemangioblastoma with late leptomeningeal metastasis: a case report Poiset, Spencer J. Reddy, Aneesh Tucker, Catherine M. Kenyon, Lawrence C. Judy, Kevin D. Shi, Wenyin J Med Case Rep Case Report BACKGROUND: Hemangioblastoma of the central nervous system is an uncommon benign neoplasm, with about 25% of cases in patients with von Hippel–Lindau disease. The incidence of metastasis is rare, particularly in patients without von Hippel–Lindau disease. We report a case of hemangioblastoma with leptomeningeal dissemination as a late recurrence. CASE PRESENTATION: A 65-year-old Caucasian man with a history of World Health Organization grade I hemangioblastoma of the cerebellar vermis underwent gross total resection in 1997. In early 2018, he developed intracranial recurrences with diffuse leptomeningeal disease of the entire spine. The patient underwent resection of intracranial recurrence, followed by palliative craniospinal irradiation. The disease progressed quickly, and he died 8 months after recurrence. CONCLUSIONS: Despite a benign pathology, hemangioblastoma has a low risk of metastasis. The outcome for hemangioblastoma patients with metastasis is poor. Multidisciplinary care for patients with metastatic hemangioblastoma warrants further investigation, and an effective systemic option is urgently needed. Regular lifelong follow-up of at-risk patients is recommended. BioMed Central 2023-03-20 /pmc/articles/PMC10026473/ /pubmed/36935497 http://dx.doi.org/10.1186/s13256-023-03812-5 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 Poiset, Spencer J. Reddy, Aneesh Tucker, Catherine M. Kenyon, Lawrence C. Judy, Kevin D. Shi, Wenyin Hemangioblastoma with late leptomeningeal metastasis: a case report |
title | Hemangioblastoma with late leptomeningeal metastasis: a case report |
title_full | Hemangioblastoma with late leptomeningeal metastasis: a case report |
title_fullStr | Hemangioblastoma with late leptomeningeal metastasis: a case report |
title_full_unstemmed | Hemangioblastoma with late leptomeningeal metastasis: a case report |
title_short | Hemangioblastoma with late leptomeningeal metastasis: a case report |
title_sort | hemangioblastoma with late leptomeningeal metastasis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026473/ https://www.ncbi.nlm.nih.gov/pubmed/36935497 http://dx.doi.org/10.1186/s13256-023-03812-5 |
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