Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking Sarcoma
Spindle cell hemangioendothelioma (SCH) was originally described by Weiss and Enzinger (1986) as a low-grade angiosarcoma resembling both cavernous hemangioma and Kaposi's sarcoma. Recent studies suggest that SCH is a benign neoplasm or reactive lesion accompanying a congenital or acquired vasc...
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2011-01-01
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Series: | Case Reports in Surgery |
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doaj-07e7fbc6b1ea4f9a97bdd60ad90e0a272020-11-24T23:47:49ZengHindawi LimitedCase Reports in Surgery2090-69002090-69192011-01-01201110.1155/2011/481654481654Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking SarcomaTomohiro Minagawa0Takeshi Yamao1Ryuta Shioya2Department of Plastic and Reconstructive Surgery, Asahikawa Kosei General Hospital, Hokkaido, Asahikawa 078-8211, JapanDepartment of Plastic and Reconstructive Surgery, Hokkaido University Graduate School of Medicine, Hokkaido, Sapporo 060-0815, JapanDepartment of Plastic and Reconstructive Surgery, Hokkaido University Graduate School of Medicine, Hokkaido, Sapporo 060-0815, JapanSpindle cell hemangioendothelioma (SCH) was originally described by Weiss and Enzinger (1986) as a low-grade angiosarcoma resembling both cavernous hemangioma and Kaposi's sarcoma. Recent studies suggest that SCH is a benign neoplasm or reactive lesion accompanying a congenital or acquired vascular malformation. Most SCHs present as one or more nodules affecting the dermis or subcutis of the distal extremities. Few reports describe SCH of the head and neck region; even fewer note intramuscular SCH. Here, we describe a case of SCH involving the temporal muscle mimicking soft tissue sarcoma, who had a successful surgical treatment with a coronal approach and zygomatic osteotomy.http://dx.doi.org/10.1155/2011/481654 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tomohiro Minagawa Takeshi Yamao Ryuta Shioya |
spellingShingle |
Tomohiro Minagawa Takeshi Yamao Ryuta Shioya Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking Sarcoma Case Reports in Surgery |
author_facet |
Tomohiro Minagawa Takeshi Yamao Ryuta Shioya |
author_sort |
Tomohiro Minagawa |
title |
Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking Sarcoma |
title_short |
Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking Sarcoma |
title_full |
Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking Sarcoma |
title_fullStr |
Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking Sarcoma |
title_full_unstemmed |
Spindle Cell Hemangioendothelioma of the Temporal Muscle Resected with Zygomatic Osteotomy: A Case Report of an Unusual Intramuscular Lesion Mimicking Sarcoma |
title_sort |
spindle cell hemangioendothelioma of the temporal muscle resected with zygomatic osteotomy: a case report of an unusual intramuscular lesion mimicking sarcoma |
publisher |
Hindawi Limited |
series |
Case Reports in Surgery |
issn |
2090-6900 2090-6919 |
publishDate |
2011-01-01 |
description |
Spindle cell hemangioendothelioma (SCH) was originally described by Weiss and Enzinger (1986) as a low-grade angiosarcoma resembling both cavernous hemangioma and Kaposi's sarcoma. Recent studies suggest that SCH is a benign neoplasm or reactive lesion accompanying a congenital or acquired vascular malformation. Most SCHs present as one or more nodules affecting the dermis or subcutis of the distal extremities. Few reports describe SCH of the head and neck region; even fewer note intramuscular SCH. Here, we describe a case of SCH involving the temporal muscle mimicking soft tissue sarcoma, who had a successful surgical treatment with a coronal approach and zygomatic osteotomy. |
url |
http://dx.doi.org/10.1155/2011/481654 |
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