AA amyloidosis

Secondary amyloidosis is a form of amyloidosis (see this term), that complicates chronic inflammatory disorders (mainly rheumatoid arthritis, see this term) and is characterized by the aggregation and deposition of amyloid fibrils composed of serum amyloid A protein, an acute phase reactant. Although spleen, suprarenal gland, liver and gut are frequent sites of amyloid deposition, the clinical picture is dominated by renal involvement.

Myocardial infarction

Necrosis of the myocardium caused by an obstruction of the blood supply to the heart and often associated with chest pain, shortness of breath, palpitations, and anxiety as well as characteristic EKG findings and elevation of serum markers including creatine kinase-MB fraction and troponin.


Total: 1

                      


(per page)
PMID (PMCID)
2058151
FEMALE Middle Aged
[Myocardial rupture in primary chronic polyarthritis. Sequela of a rare combination of acute myocardial infarct, secondary amyloidosis and perimyocarditis].
Ljuba M, Philippitsch G.
Wien Med Wochenschr. 1991;141(3):58-60.
This is the report of a patient with malignant chronic rheumatoid arthritis complicated by an acute myocardial infarction, left ventricular wall rupture and pseudoaneurysm besides reactive amyloidosis and perimyocarditis.