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19 Months Toddler with a Giant Oral Capillary Hemangioma, a Case Report

Head and neck vascular tumors are common in children. Capillary hemangiomas are often easily confused with pyogenic granulomas due to histopathological resemblance. Furthermore, predisposing factors to pyogenic granulomas include an existing hemangioma, which may be co-existing entities. Surgical ex...

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Autores principales: Kabagenyi, Fiona, Anena, Sandra Petti, Seguya, Amina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198171/
https://www.ncbi.nlm.nih.gov/pubmed/37213705
http://dx.doi.org/10.2147/IMCRJ.S406901
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author Kabagenyi, Fiona
Anena, Sandra Petti
Seguya, Amina
author_facet Kabagenyi, Fiona
Anena, Sandra Petti
Seguya, Amina
author_sort Kabagenyi, Fiona
collection PubMed
description Head and neck vascular tumors are common in children. Capillary hemangiomas are often easily confused with pyogenic granulomas due to histopathological resemblance. Furthermore, predisposing factors to pyogenic granulomas include an existing hemangioma, which may be co-existing entities. Surgical excision of large unsightly tumors causing functional deficits is a feasible management option. We report a case of a rapidly growing oral lesion in a toddler with feeding difficulties and anemia. It triggered a diagnostic dilemma as it was clinically consistent with a pyogenic granuloma but histologically diagnosed as a capillary hemangioma. It was successfully excised with no recurrence after 6 months.
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spelling pubmed-101981712023-05-20 19 Months Toddler with a Giant Oral Capillary Hemangioma, a Case Report Kabagenyi, Fiona Anena, Sandra Petti Seguya, Amina Int Med Case Rep J Case Report Head and neck vascular tumors are common in children. Capillary hemangiomas are often easily confused with pyogenic granulomas due to histopathological resemblance. Furthermore, predisposing factors to pyogenic granulomas include an existing hemangioma, which may be co-existing entities. Surgical excision of large unsightly tumors causing functional deficits is a feasible management option. We report a case of a rapidly growing oral lesion in a toddler with feeding difficulties and anemia. It triggered a diagnostic dilemma as it was clinically consistent with a pyogenic granuloma but histologically diagnosed as a capillary hemangioma. It was successfully excised with no recurrence after 6 months. Dove 2023-05-15 /pmc/articles/PMC10198171/ /pubmed/37213705 http://dx.doi.org/10.2147/IMCRJ.S406901 Text en © 2023 Kabagenyi et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Case Report
Kabagenyi, Fiona
Anena, Sandra Petti
Seguya, Amina
19 Months Toddler with a Giant Oral Capillary Hemangioma, a Case Report
title 19 Months Toddler with a Giant Oral Capillary Hemangioma, a Case Report
title_full 19 Months Toddler with a Giant Oral Capillary Hemangioma, a Case Report
title_fullStr 19 Months Toddler with a Giant Oral Capillary Hemangioma, a Case Report
title_full_unstemmed 19 Months Toddler with a Giant Oral Capillary Hemangioma, a Case Report
title_short 19 Months Toddler with a Giant Oral Capillary Hemangioma, a Case Report
title_sort 19 months toddler with a giant oral capillary hemangioma, a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198171/
https://www.ncbi.nlm.nih.gov/pubmed/37213705
http://dx.doi.org/10.2147/IMCRJ.S406901
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