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Spindle cell hemangioma in the infratemporal fossa: A unique case report

INTRODUCTION: Spindle cell hemangioma (SCH) is a rare vascular tumor which was first described in 1986. It affects mostly the distal extremities. The head and neck are rarely involved. This article reports the first case of SCH in the infratemporal fossa. PRESENTATION OF CASE: A 41-year-old woman pr...

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Autores principales: Oukessou, Y., Lyoubi, M., Hammouda, Y., Rouadi, S., Abada, R.L., Roubal, M., Mahtar, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736763/
https://www.ncbi.nlm.nih.gov/pubmed/33310467
http://dx.doi.org/10.1016/j.ijscr.2020.11.147
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author Oukessou, Y.
Lyoubi, M.
Hammouda, Y.
Rouadi, S.
Abada, R.L.
Roubal, M.
Mahtar, M.
author_facet Oukessou, Y.
Lyoubi, M.
Hammouda, Y.
Rouadi, S.
Abada, R.L.
Roubal, M.
Mahtar, M.
author_sort Oukessou, Y.
collection PubMed
description INTRODUCTION: Spindle cell hemangioma (SCH) is a rare vascular tumor which was first described in 1986. It affects mostly the distal extremities. The head and neck are rarely involved. This article reports the first case of SCH in the infratemporal fossa. PRESENTATION OF CASE: A 41-year-old woman presented with an 8-month history of right cheek swelling. Facial CT scan and MRI showed an intensely and heterogeneously enhancing tumor of the infratemporal fossa suggesting an angiomatous neoplasm. The mass was excised surgically through an anterior maxillary approach. The histopathological and immunohistochemistry analysis revealed a SCH. CONCLUSION: This case report presents a unique presentation of a Spindle cell hemangioma in an unexpected location of the head and neck region. it underlines the importance for clinicians and pathologists to consider the Spindle cell hemangioma as a possible etiological diagnosis of infratemporal fossa tumors.
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spelling pubmed-77367632020-12-18 Spindle cell hemangioma in the infratemporal fossa: A unique case report Oukessou, Y. Lyoubi, M. Hammouda, Y. Rouadi, S. Abada, R.L. Roubal, M. Mahtar, M. Int J Surg Case Rep Case Report INTRODUCTION: Spindle cell hemangioma (SCH) is a rare vascular tumor which was first described in 1986. It affects mostly the distal extremities. The head and neck are rarely involved. This article reports the first case of SCH in the infratemporal fossa. PRESENTATION OF CASE: A 41-year-old woman presented with an 8-month history of right cheek swelling. Facial CT scan and MRI showed an intensely and heterogeneously enhancing tumor of the infratemporal fossa suggesting an angiomatous neoplasm. The mass was excised surgically through an anterior maxillary approach. The histopathological and immunohistochemistry analysis revealed a SCH. CONCLUSION: This case report presents a unique presentation of a Spindle cell hemangioma in an unexpected location of the head and neck region. it underlines the importance for clinicians and pathologists to consider the Spindle cell hemangioma as a possible etiological diagnosis of infratemporal fossa tumors. Elsevier 2020-12-02 /pmc/articles/PMC7736763/ /pubmed/33310467 http://dx.doi.org/10.1016/j.ijscr.2020.11.147 Text en © 2020 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. http://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
Oukessou, Y.
Lyoubi, M.
Hammouda, Y.
Rouadi, S.
Abada, R.L.
Roubal, M.
Mahtar, M.
Spindle cell hemangioma in the infratemporal fossa: A unique case report
title Spindle cell hemangioma in the infratemporal fossa: A unique case report
title_full Spindle cell hemangioma in the infratemporal fossa: A unique case report
title_fullStr Spindle cell hemangioma in the infratemporal fossa: A unique case report
title_full_unstemmed Spindle cell hemangioma in the infratemporal fossa: A unique case report
title_short Spindle cell hemangioma in the infratemporal fossa: A unique case report
title_sort spindle cell hemangioma in the infratemporal fossa: a unique case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736763/
https://www.ncbi.nlm.nih.gov/pubmed/33310467
http://dx.doi.org/10.1016/j.ijscr.2020.11.147
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