Sequential Liver-Kidney Transplantation for Recurrent Liver Cysts Infection in a Patient With Autosomal Dominant Polycystic Kidney Disease: A Case Report

Issa, Zaina; Ciccarelli, Olga; Devresse, Arnaud; Kanaan, Nada; Lapique, Eva Larranaga; Greef, Julien De; Lhommel, Renaud; Kerschen, Anja; Komuta, Mina; Delire, Bénédicte; Dahlqvist, Géraldine

doi:10.1016/j.transproceed.2021.02.018

Cited by 5 publications

(3 citation statements)

References 15 publications

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“…In patients with recurrent cyst infections that severely compromise quality of life, liver transplantation may be considered. 100,101 Should antibiotics/probiotics be used in hepatic cyst infection to prevent recurrence?…”

Section: Recommendationsmentioning

confidence: 99%

EASL Clinical Practice Guidelines on the management of cystic liver diseases

Drenth¹,

Barten²,

Hartog³

et al. 2022

Journal of Hepatology

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Section: Recommendationsmentioning

confidence: 99%

EASL Clinical Practice Guidelines on the management of cystic liver diseases

Drenth¹,

Barten²,

Hartog³

et al. 2022

Journal of Hepatology

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“…after renal transplantation in ADPKD, are at risk of recurrence. In patients with recurrent cyst infections that severely compromise quality of life, liver transplantation may be considered 100,101 .…”

Section: Which Antibiotic Therapy Is Recommended In Cyst Infection? R...mentioning

confidence: 99%

Clinical guidance for polycystic liver disease

Barten

2023

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Polycystic liver disease is characterized by fluid-filled cysts in the liver. Pressure from these cysts on surrounding structures causes symptoms. The severity of this disease can be determined using the total liver volume or by recording the symptom burden. This thesis demonstrates the speed and precision of various (semi-)automatic methods to calculate total liver volume. It also improves the clinical application of a polycystic liver disease specific symptom questionnaire (the PLD-Q) and demonstrates the prognostic value of total liver volume. Finally, this thesis provides clinical guidelines regarding abdominal wall hernias, diagnosis and treatment of cystic liver diseases, and future therapeutic targets for polycystic liver disease.

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“… 46 In patients with end-stage ADPKD and PLD, simultaneous or sequential RT and LT are being performed successfully with excellent outcomes ( Figure 5 ). 47 , 48 …”

Section: Pld With Adpkdmentioning

confidence: 99%

Surgical Management of Autosomal Dominant Polycystic Kidney Disease: Principles and Current Practice

Shrestha

2023

J Nepal Med Assoc

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Autosomal dominant polycystic kidney disease is the third most common cause of renal failure with no definitive treatment available that can directly target the development and growth of the cysts. Endeavours are being made to retard the growth of the cysts and preservation of renal function through medical treatment. However, 50% of the autosomal dominant polycystic kidney disease-affected persons develop complications and end-stage renal disease by the age of fifty-five and need surgical intervention for the management of complications, creation of dialysis access and renal transplantation. This review highlights the principles and current practice pertinent to the surgical management of autosomal dominant polycystic kidney disease.

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Sequential Liver-Kidney Transplantation for Recurrent Liver Cysts Infection in a Patient With Autosomal Dominant Polycystic Kidney Disease: A Case Report

Cited by 5 publications

References 15 publications

EASL Clinical Practice Guidelines on the management of cystic liver diseases

EASL Clinical Practice Guidelines on the management of cystic liver diseases

Clinical guidance for polycystic liver disease

Surgical Management of Autosomal Dominant Polycystic Kidney Disease: Principles and Current Practice

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