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Congenital Progressive Mutilating Hemangioma
A 73-year-old male patient was admitted with symptoms of decompensated cardiac and pulmonary insufficiency with long-lasting history. A tumor-like formation was observed within the clinical examination, covering the whole skin of the nose, paranasal region of the left part of the face, as well as th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
ID Design 2012/DOOEL Skopje
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503742/ https://www.ncbi.nlm.nih.gov/pubmed/28698762 http://dx.doi.org/10.3889/oamjms.2017.098 |
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author | Chokoeva, Anastasiya Sokolova, Radica Lotti, Torello Wollina, Uwe Gianfaldoni, Serena Lotti, Jacopo França, Katlein Tchernev, Georgi |
author_facet | Chokoeva, Anastasiya Sokolova, Radica Lotti, Torello Wollina, Uwe Gianfaldoni, Serena Lotti, Jacopo França, Katlein Tchernev, Georgi |
author_sort | Chokoeva, Anastasiya |
collection | PubMed |
description | A 73-year-old male patient was admitted with symptoms of decompensated cardiac and pulmonary insufficiency with long-lasting history. A tumor-like formation was observed within the clinical examination, covering the whole skin of the nose, paranasal region of the left part of the face, as well as the upper and lower left eyelids. The lesion was with yellow to brownish surface and dark-reddish to violet discolored peripheral area, composed of nodular formations, smooth central surface and firm texture on palpation. The histopathological examination verified the diagnosis of hemangioma, which had been congenital, regarding the patient’s history, treated surgically about 50 years ago, with signs of recurrence. The presented patient had been treated surgically at the age of 20, without medical evidence of the type of the performed excision. The recurrence occurs almost 50 years later, at the age of 78. To the best of our knowledge, this is the first reported recurrence of infantile hemangioma, treated surgically almost 50 years ago. |
format | Online Article Text |
id | pubmed-5503742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | ID Design 2012/DOOEL Skopje |
record_format | MEDLINE/PubMed |
spelling | pubmed-55037422017-07-11 Congenital Progressive Mutilating Hemangioma Chokoeva, Anastasiya Sokolova, Radica Lotti, Torello Wollina, Uwe Gianfaldoni, Serena Lotti, Jacopo França, Katlein Tchernev, Georgi Open Access Maced J Med Sci Letter to the Editor A 73-year-old male patient was admitted with symptoms of decompensated cardiac and pulmonary insufficiency with long-lasting history. A tumor-like formation was observed within the clinical examination, covering the whole skin of the nose, paranasal region of the left part of the face, as well as the upper and lower left eyelids. The lesion was with yellow to brownish surface and dark-reddish to violet discolored peripheral area, composed of nodular formations, smooth central surface and firm texture on palpation. The histopathological examination verified the diagnosis of hemangioma, which had been congenital, regarding the patient’s history, treated surgically about 50 years ago, with signs of recurrence. The presented patient had been treated surgically at the age of 20, without medical evidence of the type of the performed excision. The recurrence occurs almost 50 years later, at the age of 78. To the best of our knowledge, this is the first reported recurrence of infantile hemangioma, treated surgically almost 50 years ago. ID Design 2012/DOOEL Skopje 2017-06-11 /pmc/articles/PMC5503742/ /pubmed/28698762 http://dx.doi.org/10.3889/oamjms.2017.098 Text en Copyright: © 2017 Anastasiya Chokoeva, Radica Sokolova, Torello Lotti, Uwe Wollina, Serena Gianfaldoni, Jacopo Lotti, Katlein França, Georgi Tchernev. http://creativecommons.org/licenses/CC BY-NC/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0). |
spellingShingle | Letter to the Editor Chokoeva, Anastasiya Sokolova, Radica Lotti, Torello Wollina, Uwe Gianfaldoni, Serena Lotti, Jacopo França, Katlein Tchernev, Georgi Congenital Progressive Mutilating Hemangioma |
title | Congenital Progressive Mutilating Hemangioma |
title_full | Congenital Progressive Mutilating Hemangioma |
title_fullStr | Congenital Progressive Mutilating Hemangioma |
title_full_unstemmed | Congenital Progressive Mutilating Hemangioma |
title_short | Congenital Progressive Mutilating Hemangioma |
title_sort | congenital progressive mutilating hemangioma |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503742/ https://www.ncbi.nlm.nih.gov/pubmed/28698762 http://dx.doi.org/10.3889/oamjms.2017.098 |
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