Diagnosis often needs to be made on transbronchial or needle biopsy. Primary lung lymphoma represents 3.6% of extranodal lymphomas.
70-80% are marginal zone B-cell lymphomas of the mucosa-associated lymphoid tissue (MALT) (see extranodal marginal zone lymphoma)3. Lymphoepithelial lesions are present (14/141). Co-expression of CD20 and CD43 is common (10/141) and help to differentiated from lymphoid hyperplasia. Intra-lymphatic extension may occur (4/141). They are also CD5-, CD10- & bcl-2+
The most common differential is nodular reactive lymphoid hyperplasia. There is a mix of T and B lymphocyte. Lymphoepithelial lesions are common (6/101) but the lymphocytes are either CD20+/CD43- or CD3+/CD43+
Mantle cell lymphoma: positive for CD5, cyclin D1 and IgD but negative for CD10, CD23 and bcl-6.
Follicular lymphoma: positive for both CD10 and bcl-6 but negative for CD5
Primary T-cell lymphoma of the lung is rare4. Angiocentric T-cell lymphoma with associated EBV is perhaps the least uncommon T-cell lymphoma of lung5.
Prognosis
The prognosis of low grade lymphoma of the lung is good, with 94% survival at five years2.
This page last revised 20.6.2005.
©SMUHT/PW Bishop