Light chain deposition disease (pulmonary manifestations)

Last revised by Liz Silverstone on 29 Apr 2024

Pulmonary light chain deposition disease is a rare manifestation of systemic light chain deposition disease (LCDD).

Pathology

Fragments of immunoglobulin light chains secreted by a plasma clone are deposited as amorphous eosinophilic material in the alveolar walls, small airways, and vessels 2 and may involve the interlobular septa 4. LCDD is Congo Red negative (in contrast to the Congo Red positive amyloid fibrils present in amyloidosis) 5. The pathogenesis of the cysts is thought to be due to multifocal lung destruction by macrophage metalloproteinases. The macrophages are attracted to sites of protein deposition. This mechanism may explain the presence of residual tissue strands within some of the cysts 6.

Radiographic features

CT

HRCT manifestations include cysts, nodules, and lymphadenopathy 4. Cysts are usually thin-walled, spherical and perivascular with vessels in the wall or traversing the cyst 4. Zonal distribution is diffuse. Cysts may slowly increase in size and number, coalescing into irregular shapes 4.

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