Cardiac and intestinal amyloidosis in a renal transplant recipient with familial Mediterranean fever

Citation
A. Yildiz et al., Cardiac and intestinal amyloidosis in a renal transplant recipient with familial Mediterranean fever, J NEPHROL, 14(2), 2001, pp. 125-127
Citations number
17
Categorie Soggetti
Urology & Nephrology
Journal title
JOURNAL OF NEPHROLOGY
ISSN journal
11218428 → ACNP
Volume
14
Issue
2
Year of publication
2001
Pages
125 - 127
Database
ISI
SICI code
1121-8428(200103/04)14:2<125:CAIAIA>2.0.ZU;2-F
Abstract
In Turkey, familial Mediterranean fever (FMF) is an important cause of neph rotic syndrome and endstage renal disease due to renal deposition of AA typ e amyloid, We report a case of living-related donor renal transplant recipi ent with FMF and renal AA type amyloidosis, who died of progressive heart f ailure due to cardiac involvement. The patient also had intractable diarrhe a caused by biopsy-proven intestinal amyloidosis, The patient was on 1 mg/d ay colchicine, Although he was attack-free throughout the post-transplant p eriod, intestinal and clinically significant cardiac amyloidosis, which imp lied the presence of sustained inflammation and continuing amyloid depositi on, appeared three years after renal transplantation. Cardiac deposition of AA amyloid may cause clinically significant heart dis ease, leading to cardiovascular mortality after renal transplantation for e nd-stage renal disease in FMF patients.