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.

Achalasia

A disorder of esophageal motility characterized by the inability of the lower esophageal sphincter to relax during swallowing and by inadequate or lacking peristalsis in the lower half of the body of the esophagus.


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(per page)
PMID (PMCID)
2398252
MALE Middle Aged
Esophageal involvement in secondary amyloidosis mimicking achalasia.
Estrada CA, Lewandowski C, Schubert TT, Dorman PJ.
J Clin Gastroenterol. 1990;12(4):447-50.
Esophageal involvement in secondary amyloidosis mimicking achalasia.