AL amyloidosis

A plasma cell disorder characterized by the aggregation and deposition of insoluble amyloid fibrils derived from misfolding of monoclonal immunoglobulin light chains usually produced by a plasma cell tumor. It usually presents as primary systemic amyloidosis (PSA) with multiple organ involvement and less frequently as primary localized amyloidosis (PLA) restricted to a single organ.

Asthma

Asthma is characterized by increased responsiveness of the tracheobronchial tree to multiple stimuli, leading to narrowing of the air passages with resultant dyspnea, cough, and wheezing.


Total: 2

                      


(per page)
PMID (PMCID)
15072327
MALE Middle Aged
Tracheobronchial amyloidosis masquerading as bronchial asthma.
Sharma SK, Ahluwalia G, Ahluwalia A, Mukhopadhyay S.
Indian J Chest Dis Allied Sci. 2004;46(2):117-9.
A case of localized tracheobronchial primary amyloidosis masquerading as "bronchial asthma" is presented.
15072327
MALE Middle Aged
Tracheobronchial amyloidosis masquerading as bronchial asthma.
Sharma SK, Ahluwalia G, Ahluwalia A, Mukhopadhyay S.
Indian J Chest Dis Allied Sci. 2004;46(2):117-9.
Tracheobronchial primary amyloidosis is a rare, but potentially curable cause of airway obstruction mimicking asthma.