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A primary solitary vascular tumor of calcaneum: case report and review of literature
Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor with metastatic potential and estimated prevalence of less than one case per million. Among the musculoskeletal system, the long bones are commonly involved with approximately half patients experiencing multicentric involvement. Clinica...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319004/ https://www.ncbi.nlm.nih.gov/pubmed/34345331 http://dx.doi.org/10.1016/j.radcr.2021.06.045 |
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author | Patel, Zalak Meadows, Lukas Kehinde, Temitope White, Jennifer Koay |
author_facet | Patel, Zalak Meadows, Lukas Kehinde, Temitope White, Jennifer Koay |
author_sort | Patel, Zalak |
collection | PubMed |
description | Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor with metastatic potential and estimated prevalence of less than one case per million. Among the musculoskeletal system, the long bones are commonly involved with approximately half patients experiencing multicentric involvement. Clinical course of EHE is often variable and nonspecific. Poorly demarcated osteolytic lesions are most commonly seen radiologically. Diagnostic confirmation is usually obtained by biopsy and histopathological exam, including immunostaining for endothelial markers. We present a rare case of unicentric EHE involving the calcaneum. Our patient had an indolent course of disease after surgical resection and no recurrence in seven years on clinical and radiological surveillance. |
format | Online Article Text |
id | pubmed-8319004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83190042021-08-02 A primary solitary vascular tumor of calcaneum: case report and review of literature Patel, Zalak Meadows, Lukas Kehinde, Temitope White, Jennifer Koay Radiol Case Rep Case Report Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor with metastatic potential and estimated prevalence of less than one case per million. Among the musculoskeletal system, the long bones are commonly involved with approximately half patients experiencing multicentric involvement. Clinical course of EHE is often variable and nonspecific. Poorly demarcated osteolytic lesions are most commonly seen radiologically. Diagnostic confirmation is usually obtained by biopsy and histopathological exam, including immunostaining for endothelial markers. We present a rare case of unicentric EHE involving the calcaneum. Our patient had an indolent course of disease after surgical resection and no recurrence in seven years on clinical and radiological surveillance. Elsevier 2021-07-15 /pmc/articles/PMC8319004/ /pubmed/34345331 http://dx.doi.org/10.1016/j.radcr.2021.06.045 Text en Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Patel, Zalak Meadows, Lukas Kehinde, Temitope White, Jennifer Koay A primary solitary vascular tumor of calcaneum: case report and review of literature |
title | A primary solitary vascular tumor of calcaneum: case report and review of literature |
title_full | A primary solitary vascular tumor of calcaneum: case report and review of literature |
title_fullStr | A primary solitary vascular tumor of calcaneum: case report and review of literature |
title_full_unstemmed | A primary solitary vascular tumor of calcaneum: case report and review of literature |
title_short | A primary solitary vascular tumor of calcaneum: case report and review of literature |
title_sort | primary solitary vascular tumor of calcaneum: case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319004/ https://www.ncbi.nlm.nih.gov/pubmed/34345331 http://dx.doi.org/10.1016/j.radcr.2021.06.045 |
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