Thymoma: a case report and review of the literature

Thymomas comprise about 1% of all mediastinal tumours and are rare in children. Typically, these tumours are aggressive, with a poor outcome. The current treatment of invasive thymoma is often multidisciplinary. We report a 16-year-old boy with invasive thymoma who was successfully treated with s...

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Main Authors: Hamidah A,, Poulsaeman V,, Suria AA,, Zarina AL,, Zulfiqar MA,, Jamal R,
Format: Article
Language:English
Published: Penerbit UKM 2010
Online Access:http://journalarticle.ukm.my/2080/1/08MS090_4144.pdf
http://journalarticle.ukm.my/2080/
http://www.ppukm.ukm.my/ukmmcjournal/index.php
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spelling my-ukm.journal.20802016-12-14T06:30:50Z http://journalarticle.ukm.my/2080/ Thymoma: a case report and review of the literature Hamidah A, Poulsaeman V, Suria AA, Zarina AL, Zulfiqar MA, Jamal R, Thymomas comprise about 1% of all mediastinal tumours and are rare in children. Typically, these tumours are aggressive, with a poor outcome. The current treatment of invasive thymoma is often multidisciplinary. We report a 16-year-old boy with invasive thymoma who was successfully treated with systemic chemotherapy, surgical resection and irradiation. The patient has been in continuous remission for 6 years without radiographic evidence of tumour recurrence. Penerbit UKM 2010 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/2080/1/08MS090_4144.pdf Hamidah A, and Poulsaeman V, and Suria AA, and Zarina AL, and Zulfiqar MA, and Jamal R, (2010) Thymoma: a case report and review of the literature. Medicine & Health, 5 (1). pp. 49-54. ISSN 1823-2140 http://www.ppukm.ukm.my/ukmmcjournal/index.php
institution Universiti Kebangsaan Malaysia
building Perpustakaan Tun Sri Lanang Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Kebangsaan Malaysia
content_source UKM Journal Article Repository
url_provider http://journalarticle.ukm.my/
language English
description Thymomas comprise about 1% of all mediastinal tumours and are rare in children. Typically, these tumours are aggressive, with a poor outcome. The current treatment of invasive thymoma is often multidisciplinary. We report a 16-year-old boy with invasive thymoma who was successfully treated with systemic chemotherapy, surgical resection and irradiation. The patient has been in continuous remission for 6 years without radiographic evidence of tumour recurrence.
format Article
author Hamidah A,
Poulsaeman V,
Suria AA,
Zarina AL,
Zulfiqar MA,
Jamal R,
spellingShingle Hamidah A,
Poulsaeman V,
Suria AA,
Zarina AL,
Zulfiqar MA,
Jamal R,
Thymoma: a case report and review of the literature
author_facet Hamidah A,
Poulsaeman V,
Suria AA,
Zarina AL,
Zulfiqar MA,
Jamal R,
author_sort Hamidah A,
title Thymoma: a case report and review of the literature
title_short Thymoma: a case report and review of the literature
title_full Thymoma: a case report and review of the literature
title_fullStr Thymoma: a case report and review of the literature
title_full_unstemmed Thymoma: a case report and review of the literature
title_sort thymoma: a case report and review of the literature
publisher Penerbit UKM
publishDate 2010
url http://journalarticle.ukm.my/2080/1/08MS090_4144.pdf
http://journalarticle.ukm.my/2080/
http://www.ppukm.ukm.my/ukmmcjournal/index.php
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score 13.214268