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Pediatric hepatic rhabdoid tumor: A rare cause of abdominal mass in children
Pediatric hepatic rhabdoid tumors are rare tumors of the liver, with few cases reported in the literature. These aggressive tumors can be difficult to differentiate from hepatoblastomas on imaging alone, and surgical biopsy combined with special immunohistochemical stains can assist in differentiati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066605/ https://www.ncbi.nlm.nih.gov/pubmed/30065795 http://dx.doi.org/10.1016/j.radcr.2018.03.017 |
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author | Kapral, Nicole Melmer, Patrick Druzgal, Colleen Harkins Lancaster, Luke |
author_facet | Kapral, Nicole Melmer, Patrick Druzgal, Colleen Harkins Lancaster, Luke |
author_sort | Kapral, Nicole |
collection | PubMed |
description | Pediatric hepatic rhabdoid tumors are rare tumors of the liver, with few cases reported in the literature. These aggressive tumors can be difficult to differentiate from hepatoblastomas on imaging alone, and surgical biopsy combined with special immunohistochemical stains can assist in differentiating these 2 tumor types. We present a case of hepatic rhabdoid tumor in a 7-month-old female infant, which was originally thought to be a hepatoblastoma; however, using BAF47 staining for INI-1 we were able to diagnose a rhabdoid tumor and affect the patient's medical oncologic therapy. Earlier detection and a better understanding of the imaging features of hepatic rhabdoid tumor may aid in improved patient management and treatment planning. |
format | Online Article Text |
id | pubmed-6066605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-60666052018-07-31 Pediatric hepatic rhabdoid tumor: A rare cause of abdominal mass in children Kapral, Nicole Melmer, Patrick Druzgal, Colleen Harkins Lancaster, Luke Radiol Case Rep Pediatric Pediatric hepatic rhabdoid tumors are rare tumors of the liver, with few cases reported in the literature. These aggressive tumors can be difficult to differentiate from hepatoblastomas on imaging alone, and surgical biopsy combined with special immunohistochemical stains can assist in differentiating these 2 tumor types. We present a case of hepatic rhabdoid tumor in a 7-month-old female infant, which was originally thought to be a hepatoblastoma; however, using BAF47 staining for INI-1 we were able to diagnose a rhabdoid tumor and affect the patient's medical oncologic therapy. Earlier detection and a better understanding of the imaging features of hepatic rhabdoid tumor may aid in improved patient management and treatment planning. Elsevier 2018-05-10 /pmc/articles/PMC6066605/ /pubmed/30065795 http://dx.doi.org/10.1016/j.radcr.2018.03.017 Text en © 2018 the Authors. Published by Elsevier Inc. under copyright license from the University of Washington. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Pediatric Kapral, Nicole Melmer, Patrick Druzgal, Colleen Harkins Lancaster, Luke Pediatric hepatic rhabdoid tumor: A rare cause of abdominal mass in children |
title | Pediatric hepatic rhabdoid tumor: A rare cause of abdominal mass in children |
title_full | Pediatric hepatic rhabdoid tumor: A rare cause of abdominal mass in children |
title_fullStr | Pediatric hepatic rhabdoid tumor: A rare cause of abdominal mass in children |
title_full_unstemmed | Pediatric hepatic rhabdoid tumor: A rare cause of abdominal mass in children |
title_short | Pediatric hepatic rhabdoid tumor: A rare cause of abdominal mass in children |
title_sort | pediatric hepatic rhabdoid tumor: a rare cause of abdominal mass in children |
topic | Pediatric |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6066605/ https://www.ncbi.nlm.nih.gov/pubmed/30065795 http://dx.doi.org/10.1016/j.radcr.2018.03.017 |
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