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A case of middle mediastinal cavernous hemangioma

While cavernous hemangioma are frequently observed in various tissues and locations in the body, mediastinal cavernous hemangiomas (CHMs) are rare, particularly in the middle mediastinum. Here, we report a case of a middle CHM which was diagnosed and treated in our hospital. A male patient age 57 ye...

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Detalles Bibliográficos
Autores principales: Cai, Xianqi, Liu, Chunquan, Cui, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049481/
https://www.ncbi.nlm.nih.gov/pubmed/31944605
http://dx.doi.org/10.1111/1759-7714.13301
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author Cai, Xianqi
Liu, Chunquan
Cui, Yong
author_facet Cai, Xianqi
Liu, Chunquan
Cui, Yong
author_sort Cai, Xianqi
collection PubMed
description While cavernous hemangioma are frequently observed in various tissues and locations in the body, mediastinal cavernous hemangiomas (CHMs) are rare, particularly in the middle mediastinum. Here, we report a case of a middle CHM which was diagnosed and treated in our hospital. A male patient age 57 years was admitted with a mediastinal circular low‐density lesion. Preoperative examination was performed with a subsequent diagnosis of a mediastinal lesion. The lesion was resected and post‐operative histopathology suggested that it was a cavernous hemangioma. Post‐operative recovery was uneventful, and a follow‐up examination nearly one year later showed that the patient had no recurrence.
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spelling pubmed-70494812020-03-05 A case of middle mediastinal cavernous hemangioma Cai, Xianqi Liu, Chunquan Cui, Yong Thorac Cancer Case Reports While cavernous hemangioma are frequently observed in various tissues and locations in the body, mediastinal cavernous hemangiomas (CHMs) are rare, particularly in the middle mediastinum. Here, we report a case of a middle CHM which was diagnosed and treated in our hospital. A male patient age 57 years was admitted with a mediastinal circular low‐density lesion. Preoperative examination was performed with a subsequent diagnosis of a mediastinal lesion. The lesion was resected and post‐operative histopathology suggested that it was a cavernous hemangioma. Post‐operative recovery was uneventful, and a follow‐up examination nearly one year later showed that the patient had no recurrence. John Wiley & Sons Australia, Ltd 2020-01-16 2020-03 /pmc/articles/PMC7049481/ /pubmed/31944605 http://dx.doi.org/10.1111/1759-7714.13301 Text en © 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Cai, Xianqi
Liu, Chunquan
Cui, Yong
A case of middle mediastinal cavernous hemangioma
title A case of middle mediastinal cavernous hemangioma
title_full A case of middle mediastinal cavernous hemangioma
title_fullStr A case of middle mediastinal cavernous hemangioma
title_full_unstemmed A case of middle mediastinal cavernous hemangioma
title_short A case of middle mediastinal cavernous hemangioma
title_sort case of middle mediastinal cavernous hemangioma
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049481/
https://www.ncbi.nlm.nih.gov/pubmed/31944605
http://dx.doi.org/10.1111/1759-7714.13301
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