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Malignant Rhabdoid Tumor of the Liver: A Case Report and Literature Review
Malignant rhabdoid tumor (MRT) is a rare and aggressive malignancy associated with poor outcomes. MRT of the liver is even rarer, and little information has been described. We report the case of an 8-month-old boy with MRT of the liver. The tumor showed aggressive progression despite a multidiscipli...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387326/ https://www.ncbi.nlm.nih.gov/pubmed/25918621 http://dx.doi.org/10.4081/pr.2015.5578 |
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author | Oita, Satoru Terui, Keita Komatsu, Syugo Hishiki, Tomoro Saito, Takeshi Mitsunaga, Tetsuya Nakata, Mitsuyuki Yoshida, Hideo |
author_facet | Oita, Satoru Terui, Keita Komatsu, Syugo Hishiki, Tomoro Saito, Takeshi Mitsunaga, Tetsuya Nakata, Mitsuyuki Yoshida, Hideo |
author_sort | Oita, Satoru |
collection | PubMed |
description | Malignant rhabdoid tumor (MRT) is a rare and aggressive malignancy associated with poor outcomes. MRT of the liver is even rarer, and little information has been described. We report the case of an 8-month-old boy with MRT of the liver. The tumor showed aggressive progression despite a multidisciplinary approach, and the patient died due to multiple organ failure 14 days after admission. Autopsy revealed the liver tumor and multiple metastases with negative immunohistochemistry for INI1/BAF47. A review of 53 cases of pediatric MRT of the liver is provided. |
format | Online Article Text |
id | pubmed-4387326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-43873262015-04-27 Malignant Rhabdoid Tumor of the Liver: A Case Report and Literature Review Oita, Satoru Terui, Keita Komatsu, Syugo Hishiki, Tomoro Saito, Takeshi Mitsunaga, Tetsuya Nakata, Mitsuyuki Yoshida, Hideo Pediatr Rep Case Report Malignant rhabdoid tumor (MRT) is a rare and aggressive malignancy associated with poor outcomes. MRT of the liver is even rarer, and little information has been described. We report the case of an 8-month-old boy with MRT of the liver. The tumor showed aggressive progression despite a multidisciplinary approach, and the patient died due to multiple organ failure 14 days after admission. Autopsy revealed the liver tumor and multiple metastases with negative immunohistochemistry for INI1/BAF47. A review of 53 cases of pediatric MRT of the liver is provided. PAGEPress Publications, Pavia, Italy 2015-03-03 /pmc/articles/PMC4387326/ /pubmed/25918621 http://dx.doi.org/10.4081/pr.2015.5578 Text en ©Copyright S. Oita et al. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Oita, Satoru Terui, Keita Komatsu, Syugo Hishiki, Tomoro Saito, Takeshi Mitsunaga, Tetsuya Nakata, Mitsuyuki Yoshida, Hideo Malignant Rhabdoid Tumor of the Liver: A Case Report and Literature Review |
title | Malignant Rhabdoid Tumor of the Liver: A Case Report and Literature Review |
title_full | Malignant Rhabdoid Tumor of the Liver: A Case Report and Literature Review |
title_fullStr | Malignant Rhabdoid Tumor of the Liver: A Case Report and Literature Review |
title_full_unstemmed | Malignant Rhabdoid Tumor of the Liver: A Case Report and Literature Review |
title_short | Malignant Rhabdoid Tumor of the Liver: A Case Report and Literature Review |
title_sort | malignant rhabdoid tumor of the liver: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387326/ https://www.ncbi.nlm.nih.gov/pubmed/25918621 http://dx.doi.org/10.4081/pr.2015.5578 |
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