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Pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature

Cutaneous kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) are vascular tumors that are often misdiagnosed. Treatment urgency and type varies depending on which tumor-type is diagnosed, because of the differing rates of progression to Kasabach–Merritt phenomenon. An 11-month-old male pr...

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Autores principales: Sethia, Rishabh, Cerne, John W, Jatana, Kris R, Elmaraghy, Charles A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486652/
https://www.ncbi.nlm.nih.gov/pubmed/31044058
http://dx.doi.org/10.1093/jscr/rjz113
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author Sethia, Rishabh
Cerne, John W
Jatana, Kris R
Elmaraghy, Charles A
author_facet Sethia, Rishabh
Cerne, John W
Jatana, Kris R
Elmaraghy, Charles A
author_sort Sethia, Rishabh
collection PubMed
description Cutaneous kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) are vascular tumors that are often misdiagnosed. Treatment urgency and type varies depending on which tumor-type is diagnosed, because of the differing rates of progression to Kasabach–Merritt phenomenon. An 11-month-old male presented with a facial mass and biopsy results favoring a diagnosis of TA. The diagnosis of KHE, was later favored over TA given the overall clinical picture of initial rapid growth. However, serial imaging showed no subsequent growth, suggesting that clinically diagnosed KHE, may follow a benign clinical course when biopsy results suggest a diagnosis of TA.
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spelling pubmed-64866522019-05-01 Pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature Sethia, Rishabh Cerne, John W Jatana, Kris R Elmaraghy, Charles A J Surg Case Rep Case Report Cutaneous kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) are vascular tumors that are often misdiagnosed. Treatment urgency and type varies depending on which tumor-type is diagnosed, because of the differing rates of progression to Kasabach–Merritt phenomenon. An 11-month-old male presented with a facial mass and biopsy results favoring a diagnosis of TA. The diagnosis of KHE, was later favored over TA given the overall clinical picture of initial rapid growth. However, serial imaging showed no subsequent growth, suggesting that clinically diagnosed KHE, may follow a benign clinical course when biopsy results suggest a diagnosis of TA. Oxford University Press 2019-04-27 /pmc/articles/PMC6486652/ /pubmed/31044058 http://dx.doi.org/10.1093/jscr/rjz113 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2019. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Sethia, Rishabh
Cerne, John W
Jatana, Kris R
Elmaraghy, Charles A
Pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature
title Pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature
title_full Pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature
title_fullStr Pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature
title_full_unstemmed Pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature
title_short Pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature
title_sort pediatric facial kaposiform hemangioendothelioma: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486652/
https://www.ncbi.nlm.nih.gov/pubmed/31044058
http://dx.doi.org/10.1093/jscr/rjz113
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