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Recurrent Epithelioid Hemangioendothelioma of Calcaneum: A Case Report of a Rare Tumor
Epithelioid hemangioendothelioma (EHE) is an uncommon malignant vascular tumor characterized by epithelioid or histiocytoid endothelial appearance. Here we present the case of a 65-year-old female with recurrent EHE of the left calcaneum. The patient had developed soft-tissue swelling over the later...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8323439/ https://www.ncbi.nlm.nih.gov/pubmed/34345543 http://dx.doi.org/10.7759/cureus.16052 |
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author | Rustagi, Ashish Sen, Soumyadip Prasad, Rajni Krishna, Loveneesh Talwar, Jatin |
author_facet | Rustagi, Ashish Sen, Soumyadip Prasad, Rajni Krishna, Loveneesh Talwar, Jatin |
author_sort | Rustagi, Ashish |
collection | PubMed |
description | Epithelioid hemangioendothelioma (EHE) is an uncommon malignant vascular tumor characterized by epithelioid or histiocytoid endothelial appearance. Here we present the case of a 65-year-old female with recurrent EHE of the left calcaneum. The patient had developed soft-tissue swelling over the lateral aspect of the left hindfoot three years ago, which was previously managed by excisional biopsy as per medical records and the histopathological examination (HPE) had revealed an EHE. A year later, she again developed a painful swelling with superficial ulceration over the same region and presented to us. A plain radiograph of the foot showed a soft-tissue swelling with cortical breach over the lateral aspect of calcaneum. MRI revealed a mass encasing peroneus tendons, with extension into the lateral surface of calcaneum. CT angiography revealed a mass eroding the lateral cortex of calcaneum and receiving blood supply from calcaneal branches of peroneal artery. PET-CT scan did not reveal any other primary or metastatic site. Core needle biopsy of calcaneum was suggestive of EHE. Limb salvage was difficult as the tumor was recurrent and involved the skin and the weight-bearing part of the calcaneum. The patient was managed with trans-tibial amputation. Immunohistochemical (IHC) staining of the excised tissue was positive for CD34, Vimentin, SMA, and Fli-1. The margins were negative for any tumor cells and she did not require any adjuvant therapy. At two years follow-up, she was free of any further recurrence or metastasis. Recurrent tumors of this variety are fast-growing with metastatic potential and may cause mortality. Hence, they need to be managed aggressively. |
format | Online Article Text |
id | pubmed-8323439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-83234392021-08-02 Recurrent Epithelioid Hemangioendothelioma of Calcaneum: A Case Report of a Rare Tumor Rustagi, Ashish Sen, Soumyadip Prasad, Rajni Krishna, Loveneesh Talwar, Jatin Cureus Orthopedics Epithelioid hemangioendothelioma (EHE) is an uncommon malignant vascular tumor characterized by epithelioid or histiocytoid endothelial appearance. Here we present the case of a 65-year-old female with recurrent EHE of the left calcaneum. The patient had developed soft-tissue swelling over the lateral aspect of the left hindfoot three years ago, which was previously managed by excisional biopsy as per medical records and the histopathological examination (HPE) had revealed an EHE. A year later, she again developed a painful swelling with superficial ulceration over the same region and presented to us. A plain radiograph of the foot showed a soft-tissue swelling with cortical breach over the lateral aspect of calcaneum. MRI revealed a mass encasing peroneus tendons, with extension into the lateral surface of calcaneum. CT angiography revealed a mass eroding the lateral cortex of calcaneum and receiving blood supply from calcaneal branches of peroneal artery. PET-CT scan did not reveal any other primary or metastatic site. Core needle biopsy of calcaneum was suggestive of EHE. Limb salvage was difficult as the tumor was recurrent and involved the skin and the weight-bearing part of the calcaneum. The patient was managed with trans-tibial amputation. Immunohistochemical (IHC) staining of the excised tissue was positive for CD34, Vimentin, SMA, and Fli-1. The margins were negative for any tumor cells and she did not require any adjuvant therapy. At two years follow-up, she was free of any further recurrence or metastasis. Recurrent tumors of this variety are fast-growing with metastatic potential and may cause mortality. Hence, they need to be managed aggressively. Cureus 2021-06-30 /pmc/articles/PMC8323439/ /pubmed/34345543 http://dx.doi.org/10.7759/cureus.16052 Text en Copyright © 2021, Rustagi et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Orthopedics Rustagi, Ashish Sen, Soumyadip Prasad, Rajni Krishna, Loveneesh Talwar, Jatin Recurrent Epithelioid Hemangioendothelioma of Calcaneum: A Case Report of a Rare Tumor |
title | Recurrent Epithelioid Hemangioendothelioma of Calcaneum: A Case Report of a Rare Tumor |
title_full | Recurrent Epithelioid Hemangioendothelioma of Calcaneum: A Case Report of a Rare Tumor |
title_fullStr | Recurrent Epithelioid Hemangioendothelioma of Calcaneum: A Case Report of a Rare Tumor |
title_full_unstemmed | Recurrent Epithelioid Hemangioendothelioma of Calcaneum: A Case Report of a Rare Tumor |
title_short | Recurrent Epithelioid Hemangioendothelioma of Calcaneum: A Case Report of a Rare Tumor |
title_sort | recurrent epithelioid hemangioendothelioma of calcaneum: a case report of a rare tumor |
topic | Orthopedics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8323439/ https://www.ncbi.nlm.nih.gov/pubmed/34345543 http://dx.doi.org/10.7759/cureus.16052 |
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