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Radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: A case report
BACKGROUND: Rhabdoid tumours of the central nervous system are highly malignant and extremely rare in adults. To the best of our knowledge, only 87 cases of malignant rhabdoid tumour have been reported to date, inclusive of 4 cases with presumed radiation-induced aetiology. We report a case of malig...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894999/ https://www.ncbi.nlm.nih.gov/pubmed/31815097 http://dx.doi.org/10.5306/wjco.v10.i11.375 |
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author | Ng, Pei-Meng Low, Peh-Hueh Liew, Donald Ngian-San Wong, Albert Sii-Hieng |
author_facet | Ng, Pei-Meng Low, Peh-Hueh Liew, Donald Ngian-San Wong, Albert Sii-Hieng |
author_sort | Ng, Pei-Meng |
collection | PubMed |
description | BACKGROUND: Rhabdoid tumours of the central nervous system are highly malignant and extremely rare in adults. To the best of our knowledge, only 87 cases of malignant rhabdoid tumour have been reported to date, inclusive of 4 cases with presumed radiation-induced aetiology. We report a case of malignant rhabdoid tumour in an adult with presumed radiation-induced aetiology to enrich the armamentarium of this disease entity, which may have some implications for early diagnosis and treatment of this rare disease in the future. CASE SUMMARY: A 27-year-old male, who was exposed to cranial irradiation at the age of 4 years as part of the treatment for acute lymphoblastic leukaemia, presented with symptoms of raised intracranial pressure for one week. Brain magnetic resonance imaging revealed a heterogeneously enhancing lesion at the hypothalamus. Stereotactic biopsy was performed. Histopathological examination of the lesion showed malignant rhabdoid tumour. The disease progressed rapidly, with manifestation of leptomeningeal spread. He was started on craniospinal irradiation but treatment was suspended after 5.4 Gy, as he developed myelosuppression. His clinical condition deteriorated rapidly, and he succumbed to his illness within 2 mo. CONCLUSION: This fifth case of radiation-induced central nervous system rhabdoid tumour re-enforces the aggressive nature of this disease with poor prognosis. |
format | Online Article Text |
id | pubmed-6894999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-68949992019-12-06 Radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: A case report Ng, Pei-Meng Low, Peh-Hueh Liew, Donald Ngian-San Wong, Albert Sii-Hieng World J Clin Oncol Case Report BACKGROUND: Rhabdoid tumours of the central nervous system are highly malignant and extremely rare in adults. To the best of our knowledge, only 87 cases of malignant rhabdoid tumour have been reported to date, inclusive of 4 cases with presumed radiation-induced aetiology. We report a case of malignant rhabdoid tumour in an adult with presumed radiation-induced aetiology to enrich the armamentarium of this disease entity, which may have some implications for early diagnosis and treatment of this rare disease in the future. CASE SUMMARY: A 27-year-old male, who was exposed to cranial irradiation at the age of 4 years as part of the treatment for acute lymphoblastic leukaemia, presented with symptoms of raised intracranial pressure for one week. Brain magnetic resonance imaging revealed a heterogeneously enhancing lesion at the hypothalamus. Stereotactic biopsy was performed. Histopathological examination of the lesion showed malignant rhabdoid tumour. The disease progressed rapidly, with manifestation of leptomeningeal spread. He was started on craniospinal irradiation but treatment was suspended after 5.4 Gy, as he developed myelosuppression. His clinical condition deteriorated rapidly, and he succumbed to his illness within 2 mo. CONCLUSION: This fifth case of radiation-induced central nervous system rhabdoid tumour re-enforces the aggressive nature of this disease with poor prognosis. Baishideng Publishing Group Inc 2019-11-24 2019-11-24 /pmc/articles/PMC6894999/ /pubmed/31815097 http://dx.doi.org/10.5306/wjco.v10.i11.375 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Ng, Pei-Meng Low, Peh-Hueh Liew, Donald Ngian-San Wong, Albert Sii-Hieng Radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: A case report |
title | Radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: A case report |
title_full | Radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: A case report |
title_fullStr | Radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: A case report |
title_full_unstemmed | Radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: A case report |
title_short | Radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: A case report |
title_sort | radiation-induced malignant rhabdoid tumour of the hypothalamus in an adult: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894999/ https://www.ncbi.nlm.nih.gov/pubmed/31815097 http://dx.doi.org/10.5306/wjco.v10.i11.375 |
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