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A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features
BACKGROUND: Alveolar soft part sarcoma (ASPS) is a rare kind of malignant soft tissue tumor with undefined differentiation, of which the incidence rate accounts for only 0.5–1.0% among all kinds of soft tissue tumors. An even rarer ASPS occurs in kidney. CASE PRESENTATION: Here we reported a case of...
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/PMC9926823/ https://www.ncbi.nlm.nih.gov/pubmed/36782230 http://dx.doi.org/10.1186/s12894-023-01182-0 |
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author | Wang, Xue Yu, Jingjing Fan, Xiaodong Ma, Suya Xie, Xiaohong Gao, Ning Huang, Shuaishuai Lu, Aimei |
author_facet | Wang, Xue Yu, Jingjing Fan, Xiaodong Ma, Suya Xie, Xiaohong Gao, Ning Huang, Shuaishuai Lu, Aimei |
author_sort | Wang, Xue |
collection | PubMed |
description | BACKGROUND: Alveolar soft part sarcoma (ASPS) is a rare kind of malignant soft tissue tumor with undefined differentiation, of which the incidence rate accounts for only 0.5–1.0% among all kinds of soft tissue tumors. An even rarer ASPS occurs in kidney. CASE PRESENTATION: Here we reported a case of a 7-year-old girl diagnosed with nephrogenic ASPS, regarding the analyses of the incidence, clinical manifestation, pathology and genetic diagnosis, in order to deepen the recognition of the disease. CONCLUSIONS: ASPS is very rare, and tends to occur to young patients. It is very significant to precisely diagnose ASPS at an early stage, which will be the key point for the following treatment choices and prognosis. |
format | Online Article Text |
id | pubmed-9926823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99268232023-02-15 A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features Wang, Xue Yu, Jingjing Fan, Xiaodong Ma, Suya Xie, Xiaohong Gao, Ning Huang, Shuaishuai Lu, Aimei BMC Urol Case Report BACKGROUND: Alveolar soft part sarcoma (ASPS) is a rare kind of malignant soft tissue tumor with undefined differentiation, of which the incidence rate accounts for only 0.5–1.0% among all kinds of soft tissue tumors. An even rarer ASPS occurs in kidney. CASE PRESENTATION: Here we reported a case of a 7-year-old girl diagnosed with nephrogenic ASPS, regarding the analyses of the incidence, clinical manifestation, pathology and genetic diagnosis, in order to deepen the recognition of the disease. CONCLUSIONS: ASPS is very rare, and tends to occur to young patients. It is very significant to precisely diagnose ASPS at an early stage, which will be the key point for the following treatment choices and prognosis. BioMed Central 2023-02-13 /pmc/articles/PMC9926823/ /pubmed/36782230 http://dx.doi.org/10.1186/s12894-023-01182-0 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 Wang, Xue Yu, Jingjing Fan, Xiaodong Ma, Suya Xie, Xiaohong Gao, Ning Huang, Shuaishuai Lu, Aimei A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features |
title | A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features |
title_full | A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features |
title_fullStr | A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features |
title_full_unstemmed | A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features |
title_short | A case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features |
title_sort | case report and literature review on nephrogenic alveolar soft part sarcoma: clinicopathological manifestations and genetic features |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926823/ https://www.ncbi.nlm.nih.gov/pubmed/36782230 http://dx.doi.org/10.1186/s12894-023-01182-0 |
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