A case of a pulmonary mucosa‐associated lymphoid tissue lymphoma with chromosomal aberration (49, XX, +3, +i(6)(p10), +mar)
| Autor: | Naoya Kitamura, Yoshifumi Shimada, Yushi Akemoto, Naoki Yoshimura, Takahiro Homma, Toshihiro Ojima |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2019 |
| Předmět: |
lcsh:RC705-779
Pulmonary and Respiratory Medicine medicine.medical_specialty Pathology business.industry Marker chromosome Aberration of chromosome 6 marker chromosome MALT lymphoma Karyotype Case Report lcsh:Diseases of the respiratory system Case Reports trisomy 3 medicine.disease Lymphoma karyotype Lymphatic system Chromosome 3 Cardiothoracic surgery Medicine Immunohistochemistry pulmonary MALT lymphoma business |
| Zdroj: | Respirology Case Reports Respirology Case Reports, Vol 7, Iss 9, Pp n/a-n/a (2019) |
| ISSN: | 2051-3380 |
| Popis: | 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). |
| Databáze: | OpenAIRE |
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