Multifocal Epithelioid Hemangioendothelioma of the Foot and Ankle: A Case Report

We report on a 41-year-old man with multiple epithelioid hemangioendothelioma of the left foot and ankle. The patient was treated with curettage and fixation with 2 separate plates, but later developed local infection. Owing to the potential for malignancy, below-knee amputation was suggested, but t...

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Main Authors: Ilias Bisbinas, Zacharoula Karabouta, Dimitrios Georgiannos, Vasileios Lampridis, Athanasios Badekas
Format: Article
Language:English
Published: SAGE Publishing 2014-04-01
Series:Journal of Orthopaedic Surgery
Online Access:https://doi.org/10.1177/230949901402200130
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spelling doaj-4ccd6c645f9b48938676e55f9db0e9492020-11-25T03:16:58ZengSAGE PublishingJournal of Orthopaedic Surgery2309-49902014-04-012210.1177/230949901402200130Multifocal Epithelioid Hemangioendothelioma of the Foot and Ankle: A Case ReportIlias Bisbinas0Zacharoula Karabouta1Dimitrios Georgiannos2Vasileios Lampridis3Athanasios Badekas4 A'Department in Orthopaedics and Trauma Surgery, 424 Military General Hospital, Thessaloniki, Greece Department of Paediatrics, AHEPA General Hospital, Aristotle University of Thessaloniki, Greece A'Department in Orthopaedics and Trauma Surgery, 424 Military General Hospital, Thessaloniki, Greece A'Department in Orthopaedics and Trauma Surgery, 424 Military General Hospital, Thessaloniki, Greece Orthopaedic and Trauma Department, Metropolitan Hospital, Athens, GreeceWe report on a 41-year-old man with multiple epithelioid hemangioendothelioma of the left foot and ankle. The patient was treated with curettage and fixation with 2 separate plates, but later developed local infection. Owing to the potential for malignancy, below-knee amputation was suggested, but the patient declined and was treated symptomatically with close monitoring. The patient underwent removal of the plates, excision of the distal fourth of the fibula, intralesional curettage of all lesions, and fusion of the ankle and subtalar joints with a retrograde intramedullary nail. After 5.5 years, the patient had recovered well and had no evidence of malignancy. The tumour was considered definitively benign.https://doi.org/10.1177/230949901402200130
collection DOAJ
language English
format Article
sources DOAJ
author Ilias Bisbinas
Zacharoula Karabouta
Dimitrios Georgiannos
Vasileios Lampridis
Athanasios Badekas
spellingShingle Ilias Bisbinas
Zacharoula Karabouta
Dimitrios Georgiannos
Vasileios Lampridis
Athanasios Badekas
Multifocal Epithelioid Hemangioendothelioma of the Foot and Ankle: A Case Report
Journal of Orthopaedic Surgery
author_facet Ilias Bisbinas
Zacharoula Karabouta
Dimitrios Georgiannos
Vasileios Lampridis
Athanasios Badekas
author_sort Ilias Bisbinas
title Multifocal Epithelioid Hemangioendothelioma of the Foot and Ankle: A Case Report
title_short Multifocal Epithelioid Hemangioendothelioma of the Foot and Ankle: A Case Report
title_full Multifocal Epithelioid Hemangioendothelioma of the Foot and Ankle: A Case Report
title_fullStr Multifocal Epithelioid Hemangioendothelioma of the Foot and Ankle: A Case Report
title_full_unstemmed Multifocal Epithelioid Hemangioendothelioma of the Foot and Ankle: A Case Report
title_sort multifocal epithelioid hemangioendothelioma of the foot and ankle: a case report
publisher SAGE Publishing
series Journal of Orthopaedic Surgery
issn 2309-4990
publishDate 2014-04-01
description We report on a 41-year-old man with multiple epithelioid hemangioendothelioma of the left foot and ankle. The patient was treated with curettage and fixation with 2 separate plates, but later developed local infection. Owing to the potential for malignancy, below-knee amputation was suggested, but the patient declined and was treated symptomatically with close monitoring. The patient underwent removal of the plates, excision of the distal fourth of the fibula, intralesional curettage of all lesions, and fusion of the ankle and subtalar joints with a retrograde intramedullary nail. After 5.5 years, the patient had recovered well and had no evidence of malignancy. The tumour was considered definitively benign.
url https://doi.org/10.1177/230949901402200130
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