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Primary pulmonary MALT-lymphoma mimicking pulmonary infection: a case report and overview on the pertinent literature

Primary pulmonary extra-nodal MALT-lymphomas are very uncommon. Clinical-radiological pattern is variable and usually non-specific and a correct diagnosis usually requires the histopathological examination. Herein we report a case of a 59-year-old man presented with dyspnea at the slightest effort a...

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Detalles Bibliográficos
Autores principales: Patricelli, Giulia, Galeone, Carla, Rapicetta, Cristian, Valli, Riccardo, Mengoli, Maria Cecilia, Carbonelli, Cristiano, Paci, Massimiliano, Lococo, Filippo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170100/
https://www.ncbi.nlm.nih.gov/pubmed/32476855
http://dx.doi.org/10.36141/svdld.v34i3.5942
Descripción
Sumario:Primary pulmonary extra-nodal MALT-lymphomas are very uncommon. Clinical-radiological pattern is variable and usually non-specific and a correct diagnosis usually requires the histopathological examination. Herein we report a case of a 59-year-old man presented with dyspnea at the slightest effort and dry cough. At imaging multiple pulmonary consolidations with interlobular septal thickenings and ground-glass opacities were disclosed, defining a crazy paving pattern. The surgical approach was necessary to reach the diagnosis of primary pulmonary low-grade marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT-lymphoma). Immunotherapy (Rituximab) and chemotherapy (Bendamustine) were started leading to a progressive improvement of the disease. (Sarcoidosis Vasc Diffuse Lung Dis 2017; 34: 260-263)