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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Main Authors: Tomohiro Minagawa, Takeshi Yamao, Ryuta Shioya
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:Case Reports in Surgery
Online Access:http://dx.doi.org/10.1155/2011/481654
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spelling 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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AT takeshiyamao spindlecellhemangioendotheliomaofthetemporalmuscleresectedwithzygomaticosteotomyacasereportofanunusualintramuscularlesionmimickingsarcoma
AT ryutashioya spindlecellhemangioendotheliomaofthetemporalmuscleresectedwithzygomaticosteotomyacasereportofanunusualintramuscularlesionmimickingsarcoma
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