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Intranodal capillary-cavernous hemangioma: Report of a very rare case

Mixed type capillary-cavernous hemangioma is a rare vascular anomaly, with an intranodal localization being extremely rare. Its finding is often accidental but may be clinically symptomatic. The diagnosis relies on histopathology, showing a proliferation of capillaries and cavernous vessels filled w...

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Detalles Bibliográficos
Autores principales: Tessieras, Jérôme, Chenaye, Jinane, Senechaud, Christophe, Banz, Yara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501482/
https://www.ncbi.nlm.nih.gov/pubmed/31105947
http://dx.doi.org/10.1177/2050313X19846710
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author Tessieras, Jérôme
Chenaye, Jinane
Senechaud, Christophe
Banz, Yara
author_facet Tessieras, Jérôme
Chenaye, Jinane
Senechaud, Christophe
Banz, Yara
author_sort Tessieras, Jérôme
collection PubMed
description Mixed type capillary-cavernous hemangioma is a rare vascular anomaly, with an intranodal localization being extremely rare. Its finding is often accidental but may be clinically symptomatic. The diagnosis relies on histopathology, showing a proliferation of capillaries and cavernous vessels filled with erythrocytes and lined by endothelial cells. Magnetic resonance imaging with enhanced and T2 STIR sequences is the most efficient imaging for diagnosing this type of hemangioma. Rarely, malignancy or another vascular lesion can be evoked as a differential diagnosis of mixed hemangioma. Treatment in this localization is often surgical, even if other possibilities exist for other areas. In this article, we describe a very rare case of intranodal capillary-cavernous hemangioma.
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spelling pubmed-65014822019-05-17 Intranodal capillary-cavernous hemangioma: Report of a very rare case Tessieras, Jérôme Chenaye, Jinane Senechaud, Christophe Banz, Yara SAGE Open Med Case Rep Case Report Mixed type capillary-cavernous hemangioma is a rare vascular anomaly, with an intranodal localization being extremely rare. Its finding is often accidental but may be clinically symptomatic. The diagnosis relies on histopathology, showing a proliferation of capillaries and cavernous vessels filled with erythrocytes and lined by endothelial cells. Magnetic resonance imaging with enhanced and T2 STIR sequences is the most efficient imaging for diagnosing this type of hemangioma. Rarely, malignancy or another vascular lesion can be evoked as a differential diagnosis of mixed hemangioma. Treatment in this localization is often surgical, even if other possibilities exist for other areas. In this article, we describe a very rare case of intranodal capillary-cavernous hemangioma. SAGE Publications 2019-05-02 /pmc/articles/PMC6501482/ /pubmed/31105947 http://dx.doi.org/10.1177/2050313X19846710 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Tessieras, Jérôme
Chenaye, Jinane
Senechaud, Christophe
Banz, Yara
Intranodal capillary-cavernous hemangioma: Report of a very rare case
title Intranodal capillary-cavernous hemangioma: Report of a very rare case
title_full Intranodal capillary-cavernous hemangioma: Report of a very rare case
title_fullStr Intranodal capillary-cavernous hemangioma: Report of a very rare case
title_full_unstemmed Intranodal capillary-cavernous hemangioma: Report of a very rare case
title_short Intranodal capillary-cavernous hemangioma: Report of a very rare case
title_sort intranodal capillary-cavernous hemangioma: report of a very rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501482/
https://www.ncbi.nlm.nih.gov/pubmed/31105947
http://dx.doi.org/10.1177/2050313X19846710
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