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Pulmonary MALT lymphoma: A case report and review of the literature

Mucosa-associated lymphoid tissue (MALT) lymphoma is an extranodal low-grade B-cell lymphoma. Pulmonary MALT lymphoma is considered to originate from bronchial MALT and is also referred to as bronchial-associated lymphoid tissue lymphoma. Pulmonary MALT lymphoma is a rare disease, but it is the most...

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Autores principales: BI, LINTAO, LI, JUN, DAN, WANG, LU, ZHENXIA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247291/
https://www.ncbi.nlm.nih.gov/pubmed/25452791
http://dx.doi.org/10.3892/etm.2014.2072
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author BI, LINTAO
LI, JUN
DAN, WANG
LU, ZHENXIA
author_facet BI, LINTAO
LI, JUN
DAN, WANG
LU, ZHENXIA
author_sort BI, LINTAO
collection PubMed
description Mucosa-associated lymphoid tissue (MALT) lymphoma is an extranodal low-grade B-cell lymphoma. Pulmonary MALT lymphoma is considered to originate from bronchial MALT and is also referred to as bronchial-associated lymphoid tissue lymphoma. Pulmonary MALT lymphoma is a rare disease, but it is the most frequent subset of primary pulmonary lymphoma. The median age at diagnosis of pulmonary MALT lymphoma is 50–60 years, with only few patients aged <30 years. This is the case report of a 19-year-old patient with pulmonary MALT lymphoma presenting with a multiple pulmonary consolidation pattern on computed tomography scans, who underwent successful chemotherapeutic treatment with a chlorambucil-based regimen.
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spelling pubmed-42472912014-12-01 Pulmonary MALT lymphoma: A case report and review of the literature BI, LINTAO LI, JUN DAN, WANG LU, ZHENXIA Exp Ther Med Articles Mucosa-associated lymphoid tissue (MALT) lymphoma is an extranodal low-grade B-cell lymphoma. Pulmonary MALT lymphoma is considered to originate from bronchial MALT and is also referred to as bronchial-associated lymphoid tissue lymphoma. Pulmonary MALT lymphoma is a rare disease, but it is the most frequent subset of primary pulmonary lymphoma. The median age at diagnosis of pulmonary MALT lymphoma is 50–60 years, with only few patients aged <30 years. This is the case report of a 19-year-old patient with pulmonary MALT lymphoma presenting with a multiple pulmonary consolidation pattern on computed tomography scans, who underwent successful chemotherapeutic treatment with a chlorambucil-based regimen. D.A. Spandidos 2015-01 2014-11-14 /pmc/articles/PMC4247291/ /pubmed/25452791 http://dx.doi.org/10.3892/etm.2014.2072 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
BI, LINTAO
LI, JUN
DAN, WANG
LU, ZHENXIA
Pulmonary MALT lymphoma: A case report and review of the literature
title Pulmonary MALT lymphoma: A case report and review of the literature
title_full Pulmonary MALT lymphoma: A case report and review of the literature
title_fullStr Pulmonary MALT lymphoma: A case report and review of the literature
title_full_unstemmed Pulmonary MALT lymphoma: A case report and review of the literature
title_short Pulmonary MALT lymphoma: A case report and review of the literature
title_sort pulmonary malt lymphoma: a case report and review of the literature
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247291/
https://www.ncbi.nlm.nih.gov/pubmed/25452791
http://dx.doi.org/10.3892/etm.2014.2072
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