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Rare spindle cell hemangioma of bone: Case report and literature review
Spindle cell hemangioma is a rare benign hemangioma. It is mainly found as small soft tissue nodules in the distal extremities, especially in the hands. The manifestation in bone is extremely rare. We present a case of spindle cell hemangioma of bone in the frontal bone. We also reviewed the literat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760178/ https://www.ncbi.nlm.nih.gov/pubmed/35059093 http://dx.doi.org/10.1016/j.radcr.2021.11.051 |
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author | Huang, Cong Zhang, Hengsheng Guan, Li Luo, Junde |
author_facet | Huang, Cong Zhang, Hengsheng Guan, Li Luo, Junde |
author_sort | Huang, Cong |
collection | PubMed |
description | Spindle cell hemangioma is a rare benign hemangioma. It is mainly found as small soft tissue nodules in the distal extremities, especially in the hands. The manifestation in bone is extremely rare. We present a case of spindle cell hemangioma of bone in the frontal bone. We also reviewed the literature to find the common imaging findings of intraosseous hamangiomas. The main manifestations of X-ray and CT were osteolytic lesions with soap bubble-like changes, and soft tissue mass formation. Magnetic resonance imaging mainly showed a lobulated mass with clear boundary, uneven hyperintense on T2WI, and obvious enhancement on contrast-enhanced scan. Surgical excision is curative. While this lesion is rare, it can be considered in the differential diagnosis if the characteristic imaging features are present. |
format | Online Article Text |
id | pubmed-8760178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-87601782022-01-19 Rare spindle cell hemangioma of bone: Case report and literature review Huang, Cong Zhang, Hengsheng Guan, Li Luo, Junde Radiol Case Rep Case Report Spindle cell hemangioma is a rare benign hemangioma. It is mainly found as small soft tissue nodules in the distal extremities, especially in the hands. The manifestation in bone is extremely rare. We present a case of spindle cell hemangioma of bone in the frontal bone. We also reviewed the literature to find the common imaging findings of intraosseous hamangiomas. The main manifestations of X-ray and CT were osteolytic lesions with soap bubble-like changes, and soft tissue mass formation. Magnetic resonance imaging mainly showed a lobulated mass with clear boundary, uneven hyperintense on T2WI, and obvious enhancement on contrast-enhanced scan. Surgical excision is curative. While this lesion is rare, it can be considered in the differential diagnosis if the characteristic imaging features are present. Elsevier 2022-01-12 /pmc/articles/PMC8760178/ /pubmed/35059093 http://dx.doi.org/10.1016/j.radcr.2021.11.051 Text en © 2021 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 Huang, Cong Zhang, Hengsheng Guan, Li Luo, Junde Rare spindle cell hemangioma of bone: Case report and literature review |
title | Rare spindle cell hemangioma of bone: Case report and literature review |
title_full | Rare spindle cell hemangioma of bone: Case report and literature review |
title_fullStr | Rare spindle cell hemangioma of bone: Case report and literature review |
title_full_unstemmed | Rare spindle cell hemangioma of bone: Case report and literature review |
title_short | Rare spindle cell hemangioma of bone: Case report and literature review |
title_sort | rare spindle cell hemangioma of bone: case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760178/ https://www.ncbi.nlm.nih.gov/pubmed/35059093 http://dx.doi.org/10.1016/j.radcr.2021.11.051 |
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