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Epithelioid Hemangioendothelioma in a Child

Epithelioid hemangioendothelioma (EHE) is a rare tumour arising from the vascular endothelium of soft-tissue, bone and viscera. Skin involvement is rare. The disease has an indolent course, with the potential for recurrence and often associated with multi-systemic localisations. We present a rare ca...

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Autores principales: Madura, C, Sacchidanand, S, Barde, Nitin G, Biligi, Dayanand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884891/
https://www.ncbi.nlm.nih.gov/pubmed/24470723
http://dx.doi.org/10.4103/0974-2077.123414
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author Madura, C
Sacchidanand, S
Barde, Nitin G
Biligi, Dayanand
author_facet Madura, C
Sacchidanand, S
Barde, Nitin G
Biligi, Dayanand
author_sort Madura, C
collection PubMed
description Epithelioid hemangioendothelioma (EHE) is a rare tumour arising from the vascular endothelium of soft-tissue, bone and viscera. Skin involvement is rare. The disease has an indolent course, with the potential for recurrence and often associated with multi-systemic localisations. We present a rare case of cutaneous EHE without systemic involvement in 9-year-old boy. The tumour was completely excised and histopathologic diagnosis was consistent with EHE. Complete systemic assessment showed no internal localisation. Wide excision is the mainstay of therapy and regular follow-up is suggested due to the potential for recurrence. The majority of documented cases of EHE is in adults and has developed in association with an underlying systemic involvement. To the best of our knowledge, this is the second reported case of isolated cutaneous EHE in paediatric age group.
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spelling pubmed-38848912014-01-27 Epithelioid Hemangioendothelioma in a Child Madura, C Sacchidanand, S Barde, Nitin G Biligi, Dayanand J Cutan Aesthet Surg Case Report Epithelioid hemangioendothelioma (EHE) is a rare tumour arising from the vascular endothelium of soft-tissue, bone and viscera. Skin involvement is rare. The disease has an indolent course, with the potential for recurrence and often associated with multi-systemic localisations. We present a rare case of cutaneous EHE without systemic involvement in 9-year-old boy. The tumour was completely excised and histopathologic diagnosis was consistent with EHE. Complete systemic assessment showed no internal localisation. Wide excision is the mainstay of therapy and regular follow-up is suggested due to the potential for recurrence. The majority of documented cases of EHE is in adults and has developed in association with an underlying systemic involvement. To the best of our knowledge, this is the second reported case of isolated cutaneous EHE in paediatric age group. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3884891/ /pubmed/24470723 http://dx.doi.org/10.4103/0974-2077.123414 Text en Copyright: © Journal of Cutaneous and Aesthetic Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Madura, C
Sacchidanand, S
Barde, Nitin G
Biligi, Dayanand
Epithelioid Hemangioendothelioma in a Child
title Epithelioid Hemangioendothelioma in a Child
title_full Epithelioid Hemangioendothelioma in a Child
title_fullStr Epithelioid Hemangioendothelioma in a Child
title_full_unstemmed Epithelioid Hemangioendothelioma in a Child
title_short Epithelioid Hemangioendothelioma in a Child
title_sort epithelioid hemangioendothelioma in a child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884891/
https://www.ncbi.nlm.nih.gov/pubmed/24470723
http://dx.doi.org/10.4103/0974-2077.123414
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