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Rare Case of Cystic Lymphangioma Transforming Into Lymphangiosarcoma: A Case Report
Cystic lymphangioma (CL) is a rare benign tumor that mainly occurs in the neck and axilla and usually occurs in children, whereas lymphangiosarcoma (LAS) is a rare invasive tumor, usually secondary to chronic lymphedema caused by various causes, with a rare malignant transformation from CL. We prese...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894725/ https://www.ncbi.nlm.nih.gov/pubmed/35251984 http://dx.doi.org/10.3389/fonc.2022.814023 |
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author | Yu, Huili Mao, Qinxiang Zhou, Lingyan Li, Jiawei Xu, Xunhua |
author_facet | Yu, Huili Mao, Qinxiang Zhou, Lingyan Li, Jiawei Xu, Xunhua |
author_sort | Yu, Huili |
collection | PubMed |
description | Cystic lymphangioma (CL) is a rare benign tumor that mainly occurs in the neck and axilla and usually occurs in children, whereas lymphangiosarcoma (LAS) is a rare invasive tumor, usually secondary to chronic lymphedema caused by various causes, with a rare malignant transformation from CL. We presented the case of a 63-year-old woman who underwent four surgical excisions for multiple recurrence of CL in the right groin. The changes of imaging and pathological examination revealed the unusual process of its gradual malignant transformation into LAS. We followed up the patient for 16 years, and she eventually died of LAS complications. |
format | Online Article Text |
id | pubmed-8894725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88947252022-03-05 Rare Case of Cystic Lymphangioma Transforming Into Lymphangiosarcoma: A Case Report Yu, Huili Mao, Qinxiang Zhou, Lingyan Li, Jiawei Xu, Xunhua Front Oncol Oncology Cystic lymphangioma (CL) is a rare benign tumor that mainly occurs in the neck and axilla and usually occurs in children, whereas lymphangiosarcoma (LAS) is a rare invasive tumor, usually secondary to chronic lymphedema caused by various causes, with a rare malignant transformation from CL. We presented the case of a 63-year-old woman who underwent four surgical excisions for multiple recurrence of CL in the right groin. The changes of imaging and pathological examination revealed the unusual process of its gradual malignant transformation into LAS. We followed up the patient for 16 years, and she eventually died of LAS complications. Frontiers Media S.A. 2022-02-18 /pmc/articles/PMC8894725/ /pubmed/35251984 http://dx.doi.org/10.3389/fonc.2022.814023 Text en Copyright © 2022 Yu, Mao, Zhou, Li and Xu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Yu, Huili Mao, Qinxiang Zhou, Lingyan Li, Jiawei Xu, Xunhua Rare Case of Cystic Lymphangioma Transforming Into Lymphangiosarcoma: A Case Report |
title | Rare Case of Cystic Lymphangioma Transforming Into Lymphangiosarcoma: A Case Report |
title_full | Rare Case of Cystic Lymphangioma Transforming Into Lymphangiosarcoma: A Case Report |
title_fullStr | Rare Case of Cystic Lymphangioma Transforming Into Lymphangiosarcoma: A Case Report |
title_full_unstemmed | Rare Case of Cystic Lymphangioma Transforming Into Lymphangiosarcoma: A Case Report |
title_short | Rare Case of Cystic Lymphangioma Transforming Into Lymphangiosarcoma: A Case Report |
title_sort | rare case of cystic lymphangioma transforming into lymphangiosarcoma: a case report |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894725/ https://www.ncbi.nlm.nih.gov/pubmed/35251984 http://dx.doi.org/10.3389/fonc.2022.814023 |
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