Case Report Laryngo-tracheobronchial amyloidosis: a case report and review of literature

Here we report an unusual case of nodular pulmonary amyloidosis and obvious ossification due to primary pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma with

Chest computed tomography (CT) showing (A) triangular high density foci in the left lobe of the lungs, stenosis and partial occlusion in upper left lung bronchi; (B)

We report a case of hepatic involvement of primary systemic (immunoglobulin light chain, AL) amyloidosis, with severe amyloid deposition in the liver.. Of note in this

Systemic Lupus Erythematosus Associated Hemophagocytic Lymphohistiocytosis: A Case Report and Literature Review.. American Journal of

This case is interesting in that both biopsies were negative in the setting of a magnetic resonance imaging (MRI) finding suggestive of cardiac amyloidosis (CA)..

Conclusions: Here we report the case of a patient with hereditary cardiac amyloidosis associated with a Pro24Ser mutation in transthyretin, which is the first case reported in

We report the case of a hospitalized patient who experienced atraumatic splenic rupture from acquired systemic AA amyloidosis, most likely resulting from chronic injection drug

AR, aortic regurgitation; AS-CA, aortic stenosis coexisting with cardiac amyloidosis; AS, aortic stenosis; ATTR, transthyretin amyloidosis; ATTRwt, wild-type transthyre-