Korean Society of Thoracic Radiology
The Korean Radiological Society
History
A 46-year-old male patient with chest abnormality
for 2 years.
Findings
Chest PA reveals ill-defined consolidation in right
upper lobe and middle lobe. Follow-up chest PA shows consolidation in the
same regions, which is slightly decreased in volume. CT scan reveals ill-defined
consolidation with air-bronchogram in right upper and middle lobes.
Discussion
The differential diagnosis of non-resolving consolidation
include bronchiolitis obliterans with organizing pneumonia, eosinophilic
pulmonary syndromes, pulmonary alveolar proteinosis, drug-induced lung
disease, and neoplastic disorders. Bronchoalveolar cell carcinoma and primary
pulmonary lymphoma are classic neoplastic disorders that may present as
focal, alveolar opacities on chest radiograph without evidence of volume
loss.
Primary pulmonary lymphomas are uncommon. Classification
of these pulmonary lymphomas is surrounded with controversy. The attempt
to classify primary pulmonary lymphomas has additionally been difficult
acknowledging the recognition in the 1980s that lymphoma may arise from
MALT. Although this rare lesion principally arises in the stomach, occasionally
it has been identified in bowel, salivary gland, thyroid gland and lung.
Accordingly, when located in the lung, this lymphoma appears to arise from
bronchus-associated lymphoid tissue (BALT).
BALT represents a low-grade B lymphocyte lymphoma
that is composed of monotonous small lymphocytes with focal plasmacytoid
features. The origin of the cell is thought to be a B lymphocyte from the
marginal zone of the lymphoid follicle. Pulmonary MALT lymphoma comprise
a distinct group of extranodal lymphomas. These low-grade lymphomas are
usually localized and frequently do not appear to progress for periods
of 10 years or more. Radiographic findings are areas of dense, persistent
consolidation. Air bronchograms were present in the vast majority. CT may
be required to demonstrate the air bronchograms, give further information
on the distribution and morphology of the lesions.
References
1. O¡¯Donnel, PG, Jackson SA, Tung KT, Hassan B, Wilkins B, Mead GM.
Radiological appreance of lymphomas arising from Mucosa-associated lymphoid
tissue (MALT) in the lung. Clinical Radiology 1998;53:258-263.
2. Chow WH, Ducheine Y, Hilfer J, Brandstetter RD. Chronic pneumonia:
Primary malignant non-Hodgkin¡¯s lymphoma of the lung arising in mucosa-associated
lymphoid tissue. Chest 1996;110:838-840.