| Literature DB >> 11692589 |
T Murakawa1, J Nakajima, M Tanaka, M Karita, S Takamoto.
Abstract
A 67-year-old asymptomatic woman was referred to our department for treatment for a left lung tumor. The tumor was 40 mm in diameter and was present in the left lower lobe. A primary low-grade B-cell lymphoma in the mucosa-associated lymphoid tissue of the lung was suspected after a trans-bronchial lung tissue biopsy. Systemic screening revealed no other organ involvement, and the tumor was considered to be a primary lung tumor. A left lower lobectomy with hilar and mediastinal lymph node sampling was performed. Pathological examination revealed centrocyte-like cells that expressed CD20. These cells had invaded the bronchiolar epithelium to form lymphoepithelial lesions. The pathological diagnosis was confirmed to be primary low-grade B-cell lymphoma in the mucosa-associated lymphoid tissue of the lung. The origin of this tumor type in the lung is relatively rare.Entities:
Mesh:
Year: 2001 PMID: 11692589 DOI: 10.1007/bf02916227
Source DB: PubMed Journal: Jpn J Thorac Cardiovasc Surg ISSN: 1344-4964