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Thymoangiolipoma: A rare histologic variant of thymolipoma in a patient with myasthenia gravis

Thymoangiolipoma is a rare, slow-growing, benign thymic neoplasm that arises from the anterior mediastinum. A 61-year-old man with the chief complaint of right eye ptosis and high serum acetylcholine receptor antibody level is presented here. The spiral computed tomography of the chest revealed a hy...

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Autores principales: Anbardar, Mohammad Hossein, Amirmoezi, Fatemeh, Amirian, Armin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768564/
https://www.ncbi.nlm.nih.gov/pubmed/33489056
http://dx.doi.org/10.1177/2036361320979215
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author Anbardar, Mohammad Hossein
Amirmoezi, Fatemeh
Amirian, Armin
author_facet Anbardar, Mohammad Hossein
Amirmoezi, Fatemeh
Amirian, Armin
author_sort Anbardar, Mohammad Hossein
collection PubMed
description Thymoangiolipoma is a rare, slow-growing, benign thymic neoplasm that arises from the anterior mediastinum. A 61-year-old man with the chief complaint of right eye ptosis and high serum acetylcholine receptor antibody level is presented here. The spiral computed tomography of the chest revealed a hypodense mass in the anterior mediastinum. Microscopic examination showed admixture of adipose tissue, thymic tissue and blood vessels with the diagnosis of thymoangiolipoma. Thymoangiolipoma is a rare histologic variant of thymolipoma which can be associated with myasthenia gravis and must be considered as a differential diagnosis in anterior mediastinal mass with fat density in radiologic evaluation.
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spelling pubmed-77685642021-01-21 Thymoangiolipoma: A rare histologic variant of thymolipoma in a patient with myasthenia gravis Anbardar, Mohammad Hossein Amirmoezi, Fatemeh Amirian, Armin Rare Tumors Case Report Thymoangiolipoma is a rare, slow-growing, benign thymic neoplasm that arises from the anterior mediastinum. A 61-year-old man with the chief complaint of right eye ptosis and high serum acetylcholine receptor antibody level is presented here. The spiral computed tomography of the chest revealed a hypodense mass in the anterior mediastinum. Microscopic examination showed admixture of adipose tissue, thymic tissue and blood vessels with the diagnosis of thymoangiolipoma. Thymoangiolipoma is a rare histologic variant of thymolipoma which can be associated with myasthenia gravis and must be considered as a differential diagnosis in anterior mediastinal mass with fat density in radiologic evaluation. SAGE Publications 2020-12-24 /pmc/articles/PMC7768564/ /pubmed/33489056 http://dx.doi.org/10.1177/2036361320979215 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://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
Anbardar, Mohammad Hossein
Amirmoezi, Fatemeh
Amirian, Armin
Thymoangiolipoma: A rare histologic variant of thymolipoma in a patient with myasthenia gravis
title Thymoangiolipoma: A rare histologic variant of thymolipoma in a patient with myasthenia gravis
title_full Thymoangiolipoma: A rare histologic variant of thymolipoma in a patient with myasthenia gravis
title_fullStr Thymoangiolipoma: A rare histologic variant of thymolipoma in a patient with myasthenia gravis
title_full_unstemmed Thymoangiolipoma: A rare histologic variant of thymolipoma in a patient with myasthenia gravis
title_short Thymoangiolipoma: A rare histologic variant of thymolipoma in a patient with myasthenia gravis
title_sort thymoangiolipoma: a rare histologic variant of thymolipoma in a patient with myasthenia gravis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768564/
https://www.ncbi.nlm.nih.gov/pubmed/33489056
http://dx.doi.org/10.1177/2036361320979215
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