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Simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary MALT lymphoma
Primary pulmonary lymphoma is a rare entity. Furthermore, simultaneous bilateral spontaneous pneumothorax (SBSP) is a very rare condition which is often related to therapeutic complications. We present, to the best of our knowledge, the first case of primary pulmonary mucosa associated lymphoid tiss...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532852/ https://www.ncbi.nlm.nih.gov/pubmed/33062114 http://dx.doi.org/10.11604/pamj.2020.37.11.24494 |
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author | Migaou, Asma Slama, Nader Njima, Manel Achour, Asma Saad, Ahmed Ben Boukhris, Sarra Fahem, Nesrine Dimassi, Sabrine Laatiri, Adnene Mhammed, Saoussen Cheikh Rouatbi, Naceur Joobeur, Sameh |
author_facet | Migaou, Asma Slama, Nader Njima, Manel Achour, Asma Saad, Ahmed Ben Boukhris, Sarra Fahem, Nesrine Dimassi, Sabrine Laatiri, Adnene Mhammed, Saoussen Cheikh Rouatbi, Naceur Joobeur, Sameh |
author_sort | Migaou, Asma |
collection | PubMed |
description | Primary pulmonary lymphoma is a rare entity. Furthermore, simultaneous bilateral spontaneous pneumothorax (SBSP) is a very rare condition which is often related to therapeutic complications. We present, to the best of our knowledge, the first case of primary pulmonary mucosa associated lymphoid tissue (MALT) lymphoma revealed by SBSP. A 50-year-old female was diagnosed with organizing pneumonia. One month later, she presented with sudden chest pain and shortness of breath due to SBSP. Bilateral chest tubes were inserted. A scan- guided right lung biopsy led to the diagnosis of primary pulmonary MALT lymphoma. The patient was treated with R-CHOP chemotherapy. The association between lymphoma and pneumothorax is extremely rare, often related to therapeutic toxicity. We report the case of SBSP as the first manifestation of primary pulmonary MALT lymphoma. |
format | Online Article Text |
id | pubmed-7532852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-75328522020-10-13 Simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary MALT lymphoma Migaou, Asma Slama, Nader Njima, Manel Achour, Asma Saad, Ahmed Ben Boukhris, Sarra Fahem, Nesrine Dimassi, Sabrine Laatiri, Adnene Mhammed, Saoussen Cheikh Rouatbi, Naceur Joobeur, Sameh Pan Afr Med J Case Report Primary pulmonary lymphoma is a rare entity. Furthermore, simultaneous bilateral spontaneous pneumothorax (SBSP) is a very rare condition which is often related to therapeutic complications. We present, to the best of our knowledge, the first case of primary pulmonary mucosa associated lymphoid tissue (MALT) lymphoma revealed by SBSP. A 50-year-old female was diagnosed with organizing pneumonia. One month later, she presented with sudden chest pain and shortness of breath due to SBSP. Bilateral chest tubes were inserted. A scan- guided right lung biopsy led to the diagnosis of primary pulmonary MALT lymphoma. The patient was treated with R-CHOP chemotherapy. The association between lymphoma and pneumothorax is extremely rare, often related to therapeutic toxicity. We report the case of SBSP as the first manifestation of primary pulmonary MALT lymphoma. The African Field Epidemiology Network 2020-09-03 /pmc/articles/PMC7532852/ /pubmed/33062114 http://dx.doi.org/10.11604/pamj.2020.37.11.24494 Text en Copyright: Asma Migaou et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Migaou, Asma Slama, Nader Njima, Manel Achour, Asma Saad, Ahmed Ben Boukhris, Sarra Fahem, Nesrine Dimassi, Sabrine Laatiri, Adnene Mhammed, Saoussen Cheikh Rouatbi, Naceur Joobeur, Sameh Simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary MALT lymphoma |
title | Simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary MALT lymphoma |
title_full | Simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary MALT lymphoma |
title_fullStr | Simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary MALT lymphoma |
title_full_unstemmed | Simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary MALT lymphoma |
title_short | Simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary MALT lymphoma |
title_sort | simultaneous bilateral spontaneous pneumothorax as the first manifestation of primary pulmonary malt lymphoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7532852/ https://www.ncbi.nlm.nih.gov/pubmed/33062114 http://dx.doi.org/10.11604/pamj.2020.37.11.24494 |
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