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A rare primary posterior mediastinal angiolipoma: A case report

Mediastinal angiolipoma is a rare benign neoplasm composed of mature adipose tissue with an abnormal vessel. Owing to its unspecific symptoms and slow progressions, the diagnosis of this disease is often delayed by clinicians. Here we present a 68-years-old-woman presented with mild chest pain radia...

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Autores principales: Soeroso, Noni Novisari, Ananda, Fannie Rizki, Dandanah, Maulidya Ayudika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556652/
https://www.ncbi.nlm.nih.gov/pubmed/34754750
http://dx.doi.org/10.1016/j.rmcr.2021.101536
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author Soeroso, Noni Novisari
Ananda, Fannie Rizki
Dandanah, Maulidya Ayudika
author_facet Soeroso, Noni Novisari
Ananda, Fannie Rizki
Dandanah, Maulidya Ayudika
author_sort Soeroso, Noni Novisari
collection PubMed
description Mediastinal angiolipoma is a rare benign neoplasm composed of mature adipose tissue with an abnormal vessel. Owing to its unspecific symptoms and slow progressions, the diagnosis of this disease is often delayed by clinicians. Here we present a 68-years-old-woman presented with mild chest pain radiates to the back with chronic dry cough. Chest imaging showed right medial posterior intrathoracic mass attached to 3rd-5th vertebrae body without bone destructions. Exploratory thoracotomy with segmentectomy was successfully performed. Histopathology examinations showed adipose tissue surrounded by a blood vessel nest, typical for angiolipoma. The patient showed rapid recovery and was discharged a week after the surgery. After two years of follow-up, the patient showed no sign of tumor recurrence and was clinically stable. This case is the first occurrence of non-infiltrating mediastinal angiolipoma reported in Southeast Asia.
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spelling pubmed-85566522021-11-08 A rare primary posterior mediastinal angiolipoma: A case report Soeroso, Noni Novisari Ananda, Fannie Rizki Dandanah, Maulidya Ayudika Respir Med Case Rep Case Report Mediastinal angiolipoma is a rare benign neoplasm composed of mature adipose tissue with an abnormal vessel. Owing to its unspecific symptoms and slow progressions, the diagnosis of this disease is often delayed by clinicians. Here we present a 68-years-old-woman presented with mild chest pain radiates to the back with chronic dry cough. Chest imaging showed right medial posterior intrathoracic mass attached to 3rd-5th vertebrae body without bone destructions. Exploratory thoracotomy with segmentectomy was successfully performed. Histopathology examinations showed adipose tissue surrounded by a blood vessel nest, typical for angiolipoma. The patient showed rapid recovery and was discharged a week after the surgery. After two years of follow-up, the patient showed no sign of tumor recurrence and was clinically stable. This case is the first occurrence of non-infiltrating mediastinal angiolipoma reported in Southeast Asia. Elsevier 2021-10-21 /pmc/articles/PMC8556652/ /pubmed/34754750 http://dx.doi.org/10.1016/j.rmcr.2021.101536 Text en © 2021 The Authors. Published by Elsevier Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Soeroso, Noni Novisari
Ananda, Fannie Rizki
Dandanah, Maulidya Ayudika
A rare primary posterior mediastinal angiolipoma: A case report
title A rare primary posterior mediastinal angiolipoma: A case report
title_full A rare primary posterior mediastinal angiolipoma: A case report
title_fullStr A rare primary posterior mediastinal angiolipoma: A case report
title_full_unstemmed A rare primary posterior mediastinal angiolipoma: A case report
title_short A rare primary posterior mediastinal angiolipoma: A case report
title_sort rare primary posterior mediastinal angiolipoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556652/
https://www.ncbi.nlm.nih.gov/pubmed/34754750
http://dx.doi.org/10.1016/j.rmcr.2021.101536
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