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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2011
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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. |
format | Online Article Text |
id | pubmed-3141690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kondotakeshi hemangiomarelatedtomaffuccisyndromeinamanacasereport |