A Rare Case of Primary Pulmonary Diffuse Large B-Cell Lymphoma Transformed from Marginal Zone Mucosa-Associated Lymphoid Tissue Lymphoma

Author:

Kiełbowski Kajetan1ORCID,Kordykiewicz Dawid1ORCID,Jesionka Janusz1,Wójcik Janusz1ORCID,Ptaszyński Konrad2,Kostopanagiotou Konstantinos3ORCID,Waloszczyk Piotr4,Wojtyś Małgorzata Edyta1ORCID

Affiliation:

1. Department of Thoracic Surgery and Transplantation, Pomeranian Medical University in Szczecin, Alfreda Sokołowskiego 11, 70-891 Szczecin, Poland

2. Department of Pathology and Forensic Medicine, University of Warmia and Mazury Olsztyn, 11-082 Olsztyn, Poland

3. Department of Thoracic Surgery, Attikon University Hospital of Athens, 12462 Athens, Greece

4. Independent Laboratory of Pathology, Zdunomed, Energetyków 2, 70-656 Szczecin, Poland

Abstract

Primary pulmonary lymphoma is a rare neoplasm characterized by the proliferation of lymphoid tissue affecting the lungs. The most common subtype is marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT). Rarely, a MALT lymphoma transforms into a diffuse large B-cell lymphoma (DLBCL). Treatment options include chemotherapy, radiotherapy, immunotherapy, and surgery. Here, we describe a patient with a primary pulmonary MALT lymphoma transforming into DLBCL. The purpose of this case report is to raise awareness of the relevant clinical and imaging features and to emphasize the need for a multidisciplinary approach to optimal management. In addition, we screened the PubMed and Embase databases for similar reports with a confirmed presence of transforming lymphoma within the lungs.

Publisher

MDPI AG

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