Literature DB >> 25577533

[Primary pulmonary mucosa-associated lymphoid tissue lymphoma: a case report].

Bartosz Kubisa1, Anna Bocheńska, Maria Piotrowska, Paweł Dec, Anna Lesińska, Anna Kubisa, Janusz Wójcik, Jarosław Pieróg, Tomasz Grodzki.   

Abstract

Primary pulmonary lymphoma accounts only 0,5% of all primary lung neoplasms. Mucosa-associated lymphoid tissue (MALT) lymphoma is a low grade B-cell extranodal lymphoma. It is a quite infrequent entity, however it constitutes from 72% to 90% of all pulmonary lung lymphomas. Long-term stimulation of bronchus-associated lymphoid tissue by antigens, smoking, inflammatory disorders or autoimmune diseases are thought to be leading to the development of MALT lymphoma. We present the case of primary pulmonary mucosa-associated lymphoid tissue lymphoma. A 76-year-old man with a history of heavy smoking (22.5 pack years) was admitted to the hospital for a further diagnostics of an abnormal finding in the right lung visualized on the chest X-ray. The diagnostic process, including imagining studies did not reveal the etiology of a lesion in the right lung. The patient was qualified for surgical diagnostics. The histological finding confirmed extranodal marginal low-grade B-cell lymphoma of mucosa -associated lymphoid tissue.

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Year:  2015        PMID: 25577533     DOI: 10.5603/PiAP.2015.0006

Source DB:  PubMed          Journal:  Pneumonol Alergol Pol        ISSN: 0867-7077


  1 in total

1.  Mesenteric lymphadenopathy is a key to diagnosis of radiologically challenging pulmonary lymphoma.

Authors:  Pei-Hsuan Lu; Chung-Yao Huang; Zong-Yi Jhou; Wei-Ming Huang; Chia-Hung Chen; Chun-Chao Huang
Journal:  Thorac Cancer       Date:  2020-04-29       Impact factor: 3.500

  1 in total

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