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Renal transplantation in amyloid nephropathy
International Urology and Nephrology
|January 1, 1989
Summary
Renal transplantation for AA-type amyloidosis shows promise, with one patient experiencing graft amyloid deposits and another maintaining excellent function. Transplantation is viable if other organs are not critically affected.
Area of Science:
- Nephrology
- Immunology
- Rheumatology
Background:
- AA-type amyloidosis is a systemic inflammatory disease that can lead to end-stage renal disease.
- Renal transplantation is a potential treatment option for patients with end-stage renal disease due to AA-type amyloidosis.
Observation:
- Two patients with end-stage renal disease due to AA-type amyloidosis underwent renal transplantation.
- One patient with rheumatoid arthritis-associated amyloidosis experienced graft amyloid deposition and died from cardiogenic shock 12 months post-transplant.
- The second patient with familial Mediterranean fever-associated amyloid nephropathy maintained excellent graft function 24 months post-transplant.
Findings:
- In a review of 33 cases (including the 2 presented), proteinuria was reported in 32.3% of patients.
- Amyloid deposition was detected in functioning grafts in 41.4% of cases.
- Graft function remained excellent even with the presence of small amyloid deposits.
Implications:
- Renal transplantation can be a successful treatment for AA-type amyloid nephropathy.
- Careful patient selection is crucial, excluding those with life-threatening amyloid involvement of other organs.
- Further research is needed to understand the long-term outcomes and management of amyloid deposition in renal grafts.