Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease

Background: The cases of mediastinal neurofibroma tumors without von Recklinghausen's disease are very rare. Clinical manifestations of tightness that do not get better with prolonged treatment using bronchodilators and steroids. After further examination and patient's history, a diagnosis...

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Main Authors: Afrita Amalia Laitupa, -, Isnin Anang Marhana, -
Format: Article PeerReviewed
Language:English
English
English
Published: Foundation for Enviromental Protection and Research 2020
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Online Access:https://repository.unair.ac.id/119961/1/Artikel%204.pdf
https://repository.unair.ac.id/119961/2/Similarity%204.pdf
https://repository.unair.ac.id/119961/3/Karil%204.pdf
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spelling id-langga.1199612023-02-14T07:22:27Z https://repository.unair.ac.id/119961/ Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease Afrita Amalia Laitupa, - Isnin Anang Marhana, - R Medicine (General) RC705-779 Diseases of the respiratory system Background: The cases of mediastinal neurofibroma tumors without von Recklinghausen's disease are very rare. Clinical manifestations of tightness that do not get better with prolonged treatment using bronchodilators and steroids. After further examination and patient's history, a diagnosis of mediastinal mass can be established, that suppress the respiratory tract. Purpose: aim to know female patients of mediastinal neurofibroma without von recklinghausen's disease. Method: Old adult patients who experience mediastinal neurofibroma tumors with symptoms of shortness of breathing that are increasingly aggravated especially when cold and fatigue. Symptoms are related to compression or invasion directly to structures around the mediastinum or associated with paraneoplastic syndrome. Asymptomatic patients are usually associated with benign tumors and vice versa patients with symptomatic usually associated with malignancy. Result: The development of a malignant tumor occurs in 10% of cases of neurofibroma especially in patients with neurofibromatosis (von Recklinghausen's disease). The duration of ongoing disease coupled with complication from other diseases makes different alternatives the best indication. Conclusion: This tumor had reached the stage of surgical therapy to achieve safe and completed tumor excision. This therapy was carried out as an optimal effort to obtain a better prognosis for the patient's disease. Foundation for Enviromental Protection and Research 2020 Article PeerReviewed text en https://repository.unair.ac.id/119961/1/Artikel%204.pdf text en https://repository.unair.ac.id/119961/2/Similarity%204.pdf text en https://repository.unair.ac.id/119961/3/Karil%204.pdf Afrita Amalia Laitupa, - and Isnin Anang Marhana, - (2020) Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease. EurAsian Journal of BioSciences, 14 (2). pp. 3115-3123. ISSN 1307-9867 https://www.proquest.com/docview/2451867832?pq-origsite=gscholar&fromopenview=true
institution Universitas Airlangga
building Universitas Airlangga Library
continent Asia
country Indonesia
Indonesia
content_provider Universitas Airlangga Library
collection UNAIR Repository
language English
English
English
topic R Medicine (General)
RC705-779 Diseases of the respiratory system
spellingShingle R Medicine (General)
RC705-779 Diseases of the respiratory system
Afrita Amalia Laitupa, -
Isnin Anang Marhana, -
Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease
description Background: The cases of mediastinal neurofibroma tumors without von Recklinghausen's disease are very rare. Clinical manifestations of tightness that do not get better with prolonged treatment using bronchodilators and steroids. After further examination and patient's history, a diagnosis of mediastinal mass can be established, that suppress the respiratory tract. Purpose: aim to know female patients of mediastinal neurofibroma without von recklinghausen's disease. Method: Old adult patients who experience mediastinal neurofibroma tumors with symptoms of shortness of breathing that are increasingly aggravated especially when cold and fatigue. Symptoms are related to compression or invasion directly to structures around the mediastinum or associated with paraneoplastic syndrome. Asymptomatic patients are usually associated with benign tumors and vice versa patients with symptomatic usually associated with malignancy. Result: The development of a malignant tumor occurs in 10% of cases of neurofibroma especially in patients with neurofibromatosis (von Recklinghausen's disease). The duration of ongoing disease coupled with complication from other diseases makes different alternatives the best indication. Conclusion: This tumor had reached the stage of surgical therapy to achieve safe and completed tumor excision. This therapy was carried out as an optimal effort to obtain a better prognosis for the patient's disease.
format Article
PeerReviewed
author Afrita Amalia Laitupa, -
Isnin Anang Marhana, -
author_facet Afrita Amalia Laitupa, -
Isnin Anang Marhana, -
author_sort Afrita Amalia Laitupa, -
title Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease
title_short Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease
title_full Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease
title_fullStr Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease
title_full_unstemmed Rare Case Report: Female patients of mediastinal neurofibroma without von Recklinghausen's disease
title_sort rare case report: female patients of mediastinal neurofibroma without von recklinghausen's disease
publisher Foundation for Enviromental Protection and Research
publishDate 2020
url https://repository.unair.ac.id/119961/1/Artikel%204.pdf
https://repository.unair.ac.id/119961/2/Similarity%204.pdf
https://repository.unair.ac.id/119961/3/Karil%204.pdf
https://repository.unair.ac.id/119961/
https://www.proquest.com/docview/2451867832?pq-origsite=gscholar&fromopenview=true
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