Thoracic Research and Practice
Case report

Low-grade B-cell Primary Pulmonary Lymphoma of Mucosa-Associated Lymphoid Tissue (MALT) Type With Synchronous Involvement Of Lacrimal Gland

1.

Atatürk Chest Diseases and Chest Surgery Education and Research Hospital, Department of Chest Diseases, Ankara, Turkey

2.

Department of Chest Disease, Hacettepe University School of Medicine, Ankara, Turkey

3.

Atatürk Chest Diseases and Chest Surgery Education and Research Hospital, Department of Chest Surgery, Ankara, Turkey

4.

Atatürk Chest Diseases and Chest Surgery Education and Research Hospital, Department of Pathology, Ankara, Turkey

Thorac Res Pract 2006; 7: Turkish Respiratory Journal 97-100
Read: 653 Downloads: 388 Published: 12 October 2021

A 52-year-old male patient was admitted to our hospital with non­productive cough, dyspnea and chest pain. He had been previously hospitalized in our facility in 2001 for the evaluation of localized con­solidation area on thorax CT. A diagnosis could not be reached by conventional methods, but he was diagnosed as MALT type lymphoma of the lacrimal gland and referred to the oncology clinic. He had re­ceived no medical care during the last five years, after which period the pulmonary lesion was stable. Histopathological examination of the resected consolidation area revealed extranodal marginal zone-B-cell lymphoma of MALT type.

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