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Papillary intralymphatic angioendothelioma: An extremely rare tumor
Papillary intralymphatic angioendothelioma (PILA), an intralymphatic lesion of vascular ducts, is an extremely rare tumor. It is generally encountered as an unexpected pathology following excision of a vascular skin lesion. Re-excision is the commonly preferred treatment option once the pathological...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bayçınar Medical Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073449/ https://www.ncbi.nlm.nih.gov/pubmed/33463445 http://dx.doi.org/10.5606/ehc.2021.78112 |
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author | Kaplan, Güven Ozan Menku Özdemir, Fethiye Damla Orhan, Diclehan Aksu, Ali Emre Özgür, Figen |
author_facet | Kaplan, Güven Ozan Menku Özdemir, Fethiye Damla Orhan, Diclehan Aksu, Ali Emre Özgür, Figen |
author_sort | Kaplan, Güven Ozan |
collection | PubMed |
description | Papillary intralymphatic angioendothelioma (PILA), an intralymphatic lesion of vascular ducts, is an extremely rare tumor. It is generally encountered as an unexpected pathology following excision of a vascular skin lesion. Re-excision is the commonly preferred treatment option once the pathological diagnosis is established. In this article, we present a 12-year-old male patient with a PILA treated with re-excision, skin grafting, and sentinel lymph node biopsy. The patient was symptom-free at annual follow-up. A sentinel lymph node biopsy during re-excision might be a good option in the surgical management of PILA. Frequent examination of lymph nodes and skin lesion also might be beneficial during the follow-ups. |
format | Online Article Text |
id | pubmed-8073449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Bayçınar Medical Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-80734492021-04-26 Papillary intralymphatic angioendothelioma: An extremely rare tumor Kaplan, Güven Ozan Menku Özdemir, Fethiye Damla Orhan, Diclehan Aksu, Ali Emre Özgür, Figen Jt Dis Relat Surg Case Report Papillary intralymphatic angioendothelioma (PILA), an intralymphatic lesion of vascular ducts, is an extremely rare tumor. It is generally encountered as an unexpected pathology following excision of a vascular skin lesion. Re-excision is the commonly preferred treatment option once the pathological diagnosis is established. In this article, we present a 12-year-old male patient with a PILA treated with re-excision, skin grafting, and sentinel lymph node biopsy. The patient was symptom-free at annual follow-up. A sentinel lymph node biopsy during re-excision might be a good option in the surgical management of PILA. Frequent examination of lymph nodes and skin lesion also might be beneficial during the follow-ups. Bayçınar Medical Publishing 2021-01-06 /pmc/articles/PMC8073449/ /pubmed/33463445 http://dx.doi.org/10.5606/ehc.2021.78112 Text en Copyright © 2021, Turkish Joint Diseases Foundation https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Report Kaplan, Güven Ozan Menku Özdemir, Fethiye Damla Orhan, Diclehan Aksu, Ali Emre Özgür, Figen Papillary intralymphatic angioendothelioma: An extremely rare tumor |
title | Papillary intralymphatic angioendothelioma: An extremely rare tumor |
title_full | Papillary intralymphatic angioendothelioma: An extremely rare tumor |
title_fullStr | Papillary intralymphatic angioendothelioma: An extremely rare tumor |
title_full_unstemmed | Papillary intralymphatic angioendothelioma: An extremely rare tumor |
title_short | Papillary intralymphatic angioendothelioma: An extremely rare tumor |
title_sort | papillary intralymphatic angioendothelioma: an extremely rare tumor |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073449/ https://www.ncbi.nlm.nih.gov/pubmed/33463445 http://dx.doi.org/10.5606/ehc.2021.78112 |
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