Aims: Giant lamellar bodies (GLBs) are rare pulmonary inclusions, most freq
uently described in sclerosing haemangiomas. Following a recent report of t
heir presence in a case of pulmonary lymphoma of MALT origin, our aims were
to determine their frequency in pulmonary lymphoproliferative disorders, e
xamine their structure and investigate their aetiology further.
Methods and results: We reviewed a series of 29 pulmonary lymphomas (23 low
-grade, six high-grade) and 18 cases of reactive pulmonary lymphoid hyperpl
asia. Five of 23 (22%) low-grade lymphomas contained GLBs, 4/4 of which sta
ined for surfactant apoprotein A but not for surfactant apoprotein B. No GL
Bs were seen in 18 cases of reactive pulmonary lymphoid hyperplasia or six
high-grade primary pulmonary lymphomas. Ultrastructural examination reveale
d concentrically arranged extracellular material forming roughly spherical
structures up to 25 mu m in diameter. The GLBs were often surrounded by foa
my cells and cholesterol clefts, supporting an origin, at least in part, fr
om products of cell breakdown and surfactant degradation.
Conclusion: These findings support the idea that the presence of lamellar b
odies is in part due to stasis of products arising from degradation of surf
actant, in association with certain types of chronic pulmonary pathology. G
iven their absence in reactive pulmonary lymphoid hyperplasia, the presence
of GLBs as an epiphenomenon in a pulmonary lymphoid infiltrate should warr
ant careful investigation with regard to the diagnosis of low-grade MALT ly
mphoma.