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Hemangioendothelioma of the sphenoid bone: a case report.

Hemangioendothelioma is borderline or intermediate type of vascular neoplasm. Hemangioendothelioma is rare lesion that constitutes less than 0.5% of the malignant tumors of bone. We present a case of low-grade hemagioendothelioma of the skull in a 29-yr-old woman. She had pain, diplopia and exophtha...

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Detalles Bibliográficos
Autores principales: Joo, M., Lee, G. J., Koh, Y. C., Park, Y. K.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054718/
https://www.ncbi.nlm.nih.gov/pubmed/11306756
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author Joo, M.
Lee, G. J.
Koh, Y. C.
Park, Y. K.
author_facet Joo, M.
Lee, G. J.
Koh, Y. C.
Park, Y. K.
author_sort Joo, M.
collection PubMed
description Hemangioendothelioma is borderline or intermediate type of vascular neoplasm. Hemangioendothelioma is rare lesion that constitutes less than 0.5% of the malignant tumors of bone. We present a case of low-grade hemagioendothelioma of the skull in a 29-yr-old woman. She had pain, diplopia and exophthalmos of the left eye. Radiographic images showed a relatively well-demarcated, expansile osteolytic lesion with irregularly thickened trabeculae and calcifications in the left greater wing of sphenoid bone. Histologically, the tumor was an infiltrative vasoformative lesion. The vessels are generally well-formed with open or compressed lumina surrounded by endothelial cells showing mild atypia. It lacked frequent mitotic figures and severe atypia. Although excessive bleeding occurred during the operation, the mass was totally resected. Postoperative radiation was not necessary. She is free of disease and well 6 months postoperatively.
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spelling pubmed-30547182011-03-15 Hemangioendothelioma of the sphenoid bone: a case report. Joo, M. Lee, G. J. Koh, Y. C. Park, Y. K. J Korean Med Sci Research Article Hemangioendothelioma is borderline or intermediate type of vascular neoplasm. Hemangioendothelioma is rare lesion that constitutes less than 0.5% of the malignant tumors of bone. We present a case of low-grade hemagioendothelioma of the skull in a 29-yr-old woman. She had pain, diplopia and exophthalmos of the left eye. Radiographic images showed a relatively well-demarcated, expansile osteolytic lesion with irregularly thickened trabeculae and calcifications in the left greater wing of sphenoid bone. Histologically, the tumor was an infiltrative vasoformative lesion. The vessels are generally well-formed with open or compressed lumina surrounded by endothelial cells showing mild atypia. It lacked frequent mitotic figures and severe atypia. Although excessive bleeding occurred during the operation, the mass was totally resected. Postoperative radiation was not necessary. She is free of disease and well 6 months postoperatively. Korean Academy of Medical Sciences 2001-04 /pmc/articles/PMC3054718/ /pubmed/11306756 Text en
spellingShingle Research Article
Joo, M.
Lee, G. J.
Koh, Y. C.
Park, Y. K.
Hemangioendothelioma of the sphenoid bone: a case report.
title Hemangioendothelioma of the sphenoid bone: a case report.
title_full Hemangioendothelioma of the sphenoid bone: a case report.
title_fullStr Hemangioendothelioma of the sphenoid bone: a case report.
title_full_unstemmed Hemangioendothelioma of the sphenoid bone: a case report.
title_short Hemangioendothelioma of the sphenoid bone: a case report.
title_sort hemangioendothelioma of the sphenoid bone: a case report.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054718/
https://www.ncbi.nlm.nih.gov/pubmed/11306756
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AT kohyc hemangioendotheliomaofthesphenoidboneacasereport
AT parkyk hemangioendotheliomaofthesphenoidboneacasereport