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Hemangioma related to Maffucci syndrome in a man: a case report

INTRODUCTION: Maffucci syndrome is a rare clinical entity (approximately 200 cases have been reported in the medical literature) with a combined occurrence of multiple enchondromas and vascular tumors. CASE PRESENTATION: The case of a 43-year-old Japanese man with multiple chondromas and hemangiomas...

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Autor principal: Kondo, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141690/
https://www.ncbi.nlm.nih.gov/pubmed/21689466
http://dx.doi.org/10.1186/1752-1947-5-224
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author Kondo, Takeshi
author_facet Kondo, Takeshi
author_sort Kondo, Takeshi
collection PubMed
description INTRODUCTION: Maffucci syndrome is a rare clinical entity (approximately 200 cases have been reported in the medical literature) with a combined occurrence of multiple enchondromas and vascular tumors. CASE PRESENTATION: The case of a 43-year-old Japanese man with multiple chondromas and hemangiomas (Maffucci syndrome) is reported. One of the hemangiomas was removed and examined pathologically. The morphological picture was an admixture of cavernous hemangioma and spindle cell hemangioma without cytological atypia or mitosis. Sheets of vacuolated endothelial cells were also observed. CONCLUSION: A rare case of hemangioma associated with Maffucci syndrome, focusing on the pathologic nature of the submitted tissue, is reported.
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spelling pubmed-31416902011-07-23 Hemangioma related to Maffucci syndrome in a man: a case report Kondo, Takeshi J Med Case Reports Case Report INTRODUCTION: Maffucci syndrome is a rare clinical entity (approximately 200 cases have been reported in the medical literature) with a combined occurrence of multiple enchondromas and vascular tumors. CASE PRESENTATION: The case of a 43-year-old Japanese man with multiple chondromas and hemangiomas (Maffucci syndrome) is reported. One of the hemangiomas was removed and examined pathologically. The morphological picture was an admixture of cavernous hemangioma and spindle cell hemangioma without cytological atypia or mitosis. Sheets of vacuolated endothelial cells were also observed. CONCLUSION: A rare case of hemangioma associated with Maffucci syndrome, focusing on the pathologic nature of the submitted tissue, is reported. BioMed Central 2011-06-21 /pmc/articles/PMC3141690/ /pubmed/21689466 http://dx.doi.org/10.1186/1752-1947-5-224 Text en Copyright ©2011 Kondo; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kondo, Takeshi
Hemangioma related to Maffucci syndrome in a man: a case report
title Hemangioma related to Maffucci syndrome in a man: a case report
title_full Hemangioma related to Maffucci syndrome in a man: a case report
title_fullStr Hemangioma related to Maffucci syndrome in a man: a case report
title_full_unstemmed Hemangioma related to Maffucci syndrome in a man: a case report
title_short Hemangioma related to Maffucci syndrome in a man: a case report
title_sort hemangioma related to maffucci syndrome in a man: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141690/
https://www.ncbi.nlm.nih.gov/pubmed/21689466
http://dx.doi.org/10.1186/1752-1947-5-224
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