A case of a pulmonary mucosa‐associated lymphoid tissue lymphoma with chromosomal aberration (49, XX, +3, +i(6)(p10), +mar). Issue 9 (25th September 2019)

• Record Type: Journal Article
• Authors: Ojima, Toshihiro; Homma, Takahiro; Shimada, Yoshifumi; Kitamura, Naoya; Akemoto, Yushi; Yoshimura, Naoki
• Is Part Of: Respirology case reports. Volume 7:Issue 9(2019)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2019-09-25
• Subjects: Aberration of chromosome 6 -- karyotype -- marker chromosome -- pulmonary MALT lymphoma -- trisomy 3; Respiratory organs -- Diseases -- Periodicals; 616.2005
• DOI: 10.1002/rcr2.489
• Languages: English
• ISSNs: 2051-3380

Abstract

Abstract : We report a case of a primary pulmonary mucosa‐associated lymphoid tissue (MALT) lymphoma with chromosomal aberration (49, XX, +3, +i(6)(p10), +mar). A 59‐year‐old woman was referred to our hospital for an abnormal chest shadow detected during a routine health check‐up in 2014. Chest computed tomography revealed a 3.2‐ × 2.3‐ × 2.0‐cm tumour shadow in the right middle lobe. Transbronchial biopsy did not result in the diagnosis of the tumour. Accordingly, as the tumour could have been malignant, right middle lobectomy was performed via video‐assisted thoracic surgery. On the basis of the results of immunohistochemical staining and gene analysis, the tumour was diagnosed as a primary pulmonary MALT lymphoma with chromosomal aberration (49, XX, +3, +i(6)(p10), +mar). Abstract : We report a case of a primary pulmonary mucosa‐associated lymphoid tissue (MALT) lymphoma with chromosomal aberration (49, XX, +3, +i(6)(p10), +mar) in a 59 year‐old woman.