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Pulmonary MALT lymphoma: A case report and review of the literature.

Abstract
Mucosa-associated lymphoid tissue (MALT) lymphoma is an extranodal low-grade B-cell lymphoma. Pulmonary MALT lymphoma is considered to originate from bronchial MALT and is also referred to as bronchial-associated lymphoid tissue lymphoma. Pulmonary MALT lymphoma is a rare disease, but it is the most frequent subset of primary pulmonary lymphoma. The median age at diagnosis of pulmonary MALT lymphoma is 50-60 years, with only few patients aged <30 years. This is the case report of a 19-year-old patient with pulmonary MALT lymphoma presenting with a multiple pulmonary consolidation pattern on computed tomography scans, who underwent successful chemotherapeutic treatment with a chlorambucil-based regimen.
AuthorsLintao Bi, Jun Li, Wang Dan, Zhenxia Lu
JournalExperimental and therapeutic medicine (Exp Ther Med) Vol. 9 Issue 1 Pg. 147-150 (Jan 2015) ISSN: 1792-0981 [Print] Greece
PMID25452791 (Publication Type: Journal Article)

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