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Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original
BACKGROUND: Infantile fibrosarcoma is a rare pediatric soft tissue tumor and usually appears in children before one year of age. Distal extremities constitute the most frequently affected locations, and other tissues such as the trunk, head and neck, gut, sacrococcygeal region, and viscera are uncom...
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/PMC10308727/ https://www.ncbi.nlm.nih.gov/pubmed/37386422 http://dx.doi.org/10.1186/s12887-023-04129-4 |
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author | Geng, Juan Chen, Dan Wang, Limin Liu, Xiangjiao Chen, Wenjing Gao, Hongyi Xiao, Shangjie |
author_facet | Geng, Juan Chen, Dan Wang, Limin Liu, Xiangjiao Chen, Wenjing Gao, Hongyi Xiao, Shangjie |
author_sort | Geng, Juan |
collection | PubMed |
description | BACKGROUND: Infantile fibrosarcoma is a rare pediatric soft tissue tumor and usually appears in children before one year of age. Distal extremities constitute the most frequently affected locations, and other tissues such as the trunk, head and neck, gut, sacrococcygeal region, and viscera are uncommon sites. CASE PRESENTATION: We describe a rare case of infantile fibrosarcoma arising from the perineum. First, a cystic mass was detected using prenatal ultrasonography, and then an echo was changed in serial ultrasound examinations. A solid cystic lesion was found at term; a hypoechoic lesion occurred in the back. The tumor became so large that massive bleeding occurred, which then underwent surgical resection. Pathological examination confirmed infantile fibrosarcoma. CONCLUSION: Our report demonstrates not all ultrasonographic findings in cases of infantile fibrosarcoma exhibit a solid mass during the initial examination — an early-stage lesion may reveal a cystic echo. Infantile fibrosarcoma has a good prognosis and surgery constitute the main treatment, with adjuvant chemotherapy being received if necessary. |
format | Online Article Text |
id | pubmed-10308727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103087272023-06-30 Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original Geng, Juan Chen, Dan Wang, Limin Liu, Xiangjiao Chen, Wenjing Gao, Hongyi Xiao, Shangjie BMC Pediatr Case Report BACKGROUND: Infantile fibrosarcoma is a rare pediatric soft tissue tumor and usually appears in children before one year of age. Distal extremities constitute the most frequently affected locations, and other tissues such as the trunk, head and neck, gut, sacrococcygeal region, and viscera are uncommon sites. CASE PRESENTATION: We describe a rare case of infantile fibrosarcoma arising from the perineum. First, a cystic mass was detected using prenatal ultrasonography, and then an echo was changed in serial ultrasound examinations. A solid cystic lesion was found at term; a hypoechoic lesion occurred in the back. The tumor became so large that massive bleeding occurred, which then underwent surgical resection. Pathological examination confirmed infantile fibrosarcoma. CONCLUSION: Our report demonstrates not all ultrasonographic findings in cases of infantile fibrosarcoma exhibit a solid mass during the initial examination — an early-stage lesion may reveal a cystic echo. Infantile fibrosarcoma has a good prognosis and surgery constitute the main treatment, with adjuvant chemotherapy being received if necessary. BioMed Central 2023-06-29 /pmc/articles/PMC10308727/ /pubmed/37386422 http://dx.doi.org/10.1186/s12887-023-04129-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Geng, Juan Chen, Dan Wang, Limin Liu, Xiangjiao Chen, Wenjing Gao, Hongyi Xiao, Shangjie Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original |
title | Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original |
title_full | Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original |
title_fullStr | Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original |
title_full_unstemmed | Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original |
title_short | Infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original |
title_sort | infantile fibrosarcoma of the perineum with dorsal metastasis in a neonate: a case report original |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10308727/ https://www.ncbi.nlm.nih.gov/pubmed/37386422 http://dx.doi.org/10.1186/s12887-023-04129-4 |
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