Published online Feb 16, 2023. doi: 10.12998/wjcc.v11.i5.1068
Peer-review started: October 9, 2022
First decision: November 4, 2022
Revised: November 22, 2022
Accepted: January 9, 2023
Article in press: January 9, 2023
Published online: February 16, 2023
Processing time: 127 Days and 18.9 Hours
Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease stemming from a deficiency in liver-specific alanine-glyoxylate aminotransferase, resulting in increased endogenous oxalate deposition and end-stage renal disease. Organ transplantation is the only effective treatment. However, its approach and timing remain controversial.
We retrospectively analyzed 5 patients diagnosed with PH1 from the Liver Transplant Center of the Beijing Friendship Hospital from March 2017 to Dec
Different transplantation strategies should be adopted for patients based on their renal function stage. Preemptive-LT offers a good therapeutic approach for PH1.
Core Tip: Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease, resulting in increased endogenous oxalate deposition and end-stage renal disease. Organ transplantation is the only effective treatment. However, the approach and timing are controversial. To investigate the effect and timing of liver transplantation (LT) for PH1, we retrospectively analyzed 5 patients. The conclusions were that LT can treat PH1, and different transplantation strategies should be adopted for patients with different renal function stages. Preemptive-LT is a more appropriate treatment.