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Nodular pulmonary amyloidosis with primary pulmonary MALT lymphoma masquerading as metastatic lung disease

Nodular pulmonary amyloidosis is a very rare form of localized amyloidosis involving the lung, with very little known about its nature. It is usually associated with indolent B cell lymphoproliferative disorder and also connective tissue disorders. No definite treatment guideline exists. Many patien...

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Autores principales: Upadhaya, Sunil, Baig, Mohd, Towfiq, Basim, Al Hadidi, Samer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538246/
https://www.ncbi.nlm.nih.gov/pubmed/28808514
http://dx.doi.org/10.1080/20009666.2017.1343075
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author Upadhaya, Sunil
Baig, Mohd
Towfiq, Basim
Al Hadidi, Samer
author_facet Upadhaya, Sunil
Baig, Mohd
Towfiq, Basim
Al Hadidi, Samer
author_sort Upadhaya, Sunil
collection PubMed
description Nodular pulmonary amyloidosis is a very rare form of localized amyloidosis involving the lung, with very little known about its nature. It is usually associated with indolent B cell lymphoproliferative disorder and also connective tissue disorders. No definite treatment guideline exists. Many patients respond to chemotherapy with low risk of progression and a ‘wait and watch’ strategy is also considered a valid treatment option. In this report the authors present a case of nodular pulmonary amyloidosis with pulmonary mucosa associated lymphoid tissue (MALT) lymphoma that presented with features of metastatic malignant disease and after definitive diagnosis decided not to undergo treatment.
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spelling pubmed-55382462017-08-14 Nodular pulmonary amyloidosis with primary pulmonary MALT lymphoma masquerading as metastatic lung disease Upadhaya, Sunil Baig, Mohd Towfiq, Basim Al Hadidi, Samer J Community Hosp Intern Med Perspect Case Reports Nodular pulmonary amyloidosis is a very rare form of localized amyloidosis involving the lung, with very little known about its nature. It is usually associated with indolent B cell lymphoproliferative disorder and also connective tissue disorders. No definite treatment guideline exists. Many patients respond to chemotherapy with low risk of progression and a ‘wait and watch’ strategy is also considered a valid treatment option. In this report the authors present a case of nodular pulmonary amyloidosis with pulmonary mucosa associated lymphoid tissue (MALT) lymphoma that presented with features of metastatic malignant disease and after definitive diagnosis decided not to undergo treatment. Taylor & Francis 2017-07-13 /pmc/articles/PMC5538246/ /pubmed/28808514 http://dx.doi.org/10.1080/20009666.2017.1343075 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Upadhaya, Sunil
Baig, Mohd
Towfiq, Basim
Al Hadidi, Samer
Nodular pulmonary amyloidosis with primary pulmonary MALT lymphoma masquerading as metastatic lung disease
title Nodular pulmonary amyloidosis with primary pulmonary MALT lymphoma masquerading as metastatic lung disease
title_full Nodular pulmonary amyloidosis with primary pulmonary MALT lymphoma masquerading as metastatic lung disease
title_fullStr Nodular pulmonary amyloidosis with primary pulmonary MALT lymphoma masquerading as metastatic lung disease
title_full_unstemmed Nodular pulmonary amyloidosis with primary pulmonary MALT lymphoma masquerading as metastatic lung disease
title_short Nodular pulmonary amyloidosis with primary pulmonary MALT lymphoma masquerading as metastatic lung disease
title_sort nodular pulmonary amyloidosis with primary pulmonary malt lymphoma masquerading as metastatic lung disease
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538246/
https://www.ncbi.nlm.nih.gov/pubmed/28808514
http://dx.doi.org/10.1080/20009666.2017.1343075
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