Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur

Kaposiform hemangioendothelioma (KHE) is a rare borderline vascular tumor that usually presents as a mass of skin or deep soft tissue. We report a unique case of an 8-year-old KHE patient with bilateral symmetrical sites involving both femurs. The laboratory, radiographic, and pathological findings...

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Detalles Bibliográficos
Autores principales: Qiu, Tong, Lan, Yuru, Zhou, Jiangyuan, Yang, Kaiying, Gong, Xue, Zhang, Zixin, Chen, Siyuan, Ji, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672085/
https://www.ncbi.nlm.nih.gov/pubmed/36405826
http://dx.doi.org/10.3389/fped.2022.995340
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author Qiu, Tong
Lan, Yuru
Zhou, Jiangyuan
Yang, Kaiying
Gong, Xue
Zhang, Zixin
Chen, Siyuan
Ji, Yi
author_facet Qiu, Tong
Lan, Yuru
Zhou, Jiangyuan
Yang, Kaiying
Gong, Xue
Zhang, Zixin
Chen, Siyuan
Ji, Yi
author_sort Qiu, Tong
collection PubMed
description Kaposiform hemangioendothelioma (KHE) is a rare borderline vascular tumor that usually presents as a mass of skin or deep soft tissue. We report a unique case of an 8-year-old KHE patient with bilateral symmetrical sites involving both femurs. The laboratory, radiographic, and pathological findings of the patient were minutely described. During the 6-month follow-up, the symptoms of pain and dysfunction of this patient were relieved. This study aimed to arouse clinicians’ concern about the symmetrical sites of KHE patients.
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spelling pubmed-96720852022-11-19 Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur Qiu, Tong Lan, Yuru Zhou, Jiangyuan Yang, Kaiying Gong, Xue Zhang, Zixin Chen, Siyuan Ji, Yi Front Pediatr Pediatrics Kaposiform hemangioendothelioma (KHE) is a rare borderline vascular tumor that usually presents as a mass of skin or deep soft tissue. We report a unique case of an 8-year-old KHE patient with bilateral symmetrical sites involving both femurs. The laboratory, radiographic, and pathological findings of the patient were minutely described. During the 6-month follow-up, the symptoms of pain and dysfunction of this patient were relieved. This study aimed to arouse clinicians’ concern about the symmetrical sites of KHE patients. Frontiers Media S.A. 2022-11-04 /pmc/articles/PMC9672085/ /pubmed/36405826 http://dx.doi.org/10.3389/fped.2022.995340 Text en © 2022 Qiu, Lan, Zhou, Yang, Gong, Zhang, Chen and Ji. 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) (https://creativecommons.org/licenses/by/4.0/) . 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 Pediatrics
Qiu, Tong
Lan, Yuru
Zhou, Jiangyuan
Yang, Kaiying
Gong, Xue
Zhang, Zixin
Chen, Siyuan
Ji, Yi
Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur
title Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur
title_full Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur
title_fullStr Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur
title_full_unstemmed Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur
title_short Case Report: Bilateral symmetrical primary kaposiform hemangioendothelioma of the femur
title_sort case report: bilateral symmetrical primary kaposiform hemangioendothelioma of the femur
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672085/
https://www.ncbi.nlm.nih.gov/pubmed/36405826
http://dx.doi.org/10.3389/fped.2022.995340
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