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Updated: Feb 11, 2026

Orthotopic Liver Transplantation in Rats
Published on: July 1, 2012
Calciphylaxis in end-stage liver and renal disease patients before and after transplant
Thomas Couri1, Matthew Stier2, Adam Mikolajczyk2
1Department of Internal Medicine, University of Chicago, Chicago, IL, USA.
Insights
Calciphylaxis, a rare vascular disorder causing tissue necrosis, is linked to end-stage renal disease (ESRD) and cirrhosis. Managing patients awaiting liver-kidney transplants requires careful consideration of high mortality rates.
Area of Science:
- Vascular Medicine
- Nephrology
- Hepatology
Background:
- Calciphylaxis is a rare, severe vascular disorder.
- Characterized by arteriole calcification, inflammation, and tissue necrosis.
- Associated with end-stage renal disease (ESRD) and cirrhosis, with high mortality (45-80% 1-year).
Purpose of the Study:
- To review the challenges in managing calciphylaxis.
- To discuss the role of kidney transplantation in calciphylaxis treatment.
- To highlight the complexities of simultaneous liver-kidney (SLK) transplantation for patients with calciphylaxis.
Main Methods:
- Literature review of calciphylaxis cases.
- Analysis of treatment outcomes and transplant considerations.
- Discussion of diagnostic criteria and clinical presentation.
Main Results:
- Calciphylaxis presents as black eschars and retiform purpura, diagnosed via skin biopsy.
- Kidney transplant can be a successful therapy, but calciphylaxis can also occur post-transplant.
- Managing patients with ESRD/cirrhosis on transplant waiting lists is complex due to high mortality.
Conclusions:
- Effective management strategies for calciphylaxis, especially concerning transplantation, are still under investigation.
- Further research is needed to optimize donor allograft allocation for patients with calciphylaxis and comorbid ESRD/cirrhosis.
- The decision-making process for SLK transplant in calciphylaxis patients requires careful risk-benefit assessment.
Abstract:
Calciphylaxis is a rare vascular disorder characterized by calcification of arterioles which causes tissue inflammation and necrosis. It is associated with the metabolic disturbances seen in end-stage renal disease (ESRD) and has also been described in patients with cirrhosis with preserved kidney function. Characteristic calciphylaxis lesions are black eschars surrounded by retiform purpura, and the gold standard for diagnosis is skin biopsy. Reported 1-year mortality rates range between 45% and 80%. No treatment modality has been evaluated in a prospective randomized trial, and reports of treatment efficacy vary. Kidney transplant has been reported as a successful therapy for calciphylaxis; however, cases exist of the initial onset of calciphylaxis following kidney transplant as well as simultaneous liver-kidney (SLK) transplant. The decision to maintain a patient with end-stage renal and liver disease on the waiting list for SLK transplant following the onset of calciphylaxis must consider the high 1-year mortality associated with this condition. More research is necessary to understand how to allocate donor allografts to manage patients with calciphylaxis and ESRD and/or cirrhosis effectively.
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