Tanrıverdi, ElifAcat, MuratÖzgül, GülerAbbaslı, KenanGül, ŞuleYaşar, Zehra2021-06-232021-06-2320171042-81941029-2403https://doi.org/10.1080/10428194.2016.1225210https://hdl.handle.net/20.500.12491/9439Primary pulmonary non-Hodgkin lymphoma is rare and constitutes up to 0.4% of all lymphomas.[1] Mucosa-associated lymphoid tissue-type (MALT) lymphoma and diffuse B-cell lymphoma are the most common types of primary pulmonary lymphoma (PPL).[2] PPL is defined as a clonal lymphoid proliferation affecting one or both lungs in a patient with no detectable extra-pulmonary involvement at diagnosis or during the subsequent 3 months.[3] Primary diffuse B-cell lymphoma constitutes as much as 10% of all PPLs.[4] Patients may be asymptomatic or have nonspecific respiratory symptoms, such as systemic constitutional symptoms and dyspnea.[1]eninfo:eu-repo/semantics/closedAccessPrimary Pulmonary LymphomaClinical ManifestationsPrimary Pulmonary Non-Hodgkin LymphomaMucosa-Associated Lymphoid Tissue-Type (MALT)Letter10.1080/10428194.2016.122521058512311233276584612-s2.0-84988556881Q2WOS:000393894000029Q2