Clinical experience of liver transplantation in the treatment of peliosis hepatis

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To the Editor:rnPeliosis hepatis (PH) is an uncommon benign vascular disorder characterized by widespread blood-filled cysts in the liver. This dis- ease was first described by Wagner in 1861, and because the liver lesions were generally red or blue-purple, it was first named PH by Schoenlack in 1916 [1] . The etiology of PH is not completely clear now, which is mainly related to drug factors, immune fac- tors, and infections. The diagnosis of PH is difficult because of the lack of specific clinical manifestations and imaging features. Patho- logical biopsy represents the gold standard in diagnosis of PH [2] . The treatment of PH varies from person to person and no consen- sus has been reached, including the removal of pathogenic factors, hepatic artery embolization, hepatectomy, etc. [3 , 4] . Liver trans- plantation (LT) may be the best treatment for PH with fatal com- plications [5 , 6] . This study described a rare case of recurrence of PH after LT.
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