Results 1 to 10 of about 31,827 (245)

Polycystic Liver Disease [PDF]

Biomedical Journal of Scientific & Technical Research
Kothadia JP, Kreitman K, Shah JM.
europepmc   +4 more sources

Simultaneous Echinococcal superinfection in a patient with polycystic liver disease [PDF]

Clinical Case Reports, 2023
Key Clinical Message Concurrent polycystic liver disease and echinococcus infection can hinder diagnosis. Surgery may be needed for accurate diagnosis and treatment. Multidisciplinary collaboration is crucial.
Ottavia Cicerone, Raffaella Lissandrin, Enrico Brunetti, Marcello Maestri   +3 more
doaj   +2 more sources

Polycystic Liver Disease: Pathophysiology, Diagnosis and Treatment [PDF]

Hepatic Medicine: Evidence and Research, 2022
Luiz Fernando Norcia,1 Erika Mayumi Watanabe,2 Pedro Tadao Hamamoto Filho,3 Claudia Nishida Hasimoto,1 Leonardo Pelafsky,1 Walmar Kerche de Oliveira,1 Ligia Yukie Sassaki4 1Department of Surgery, São Paulo State University (Unesp), Medical School ...
Norcia LF, Watanabe EM, Hamamoto Filho PT, Hasimoto CN, Pelafsky L, de Oliveira WK, Sassaki LY   +6 more
doaj   +2 more sources

Polycystic liver disease with lethal abdominal wall rupture: a case report [PDF]

Journal of Medical Case Reports, 2021
Background Polycystic liver disease is a clinical feature of autosomal dominant polycystic kidney disease, and it can sometimes cause health damage more serious than polycystic kidney.
Daichi Akuzawa, Yoichiro Uchida, Takuya Ishimura, Hiroko Kakita, Tomomi Endo, Naomi Matsuzaki, Hiroaki Terajima, Tatsuo Tsukamoto   +7 more
doaj   +2 more sources

Polycystic liver disease: An uncommon genetic condition [PDF]

Clinical Case Reports
Key Clinical Message Timely recognition, accurate diagnosis, and proper management are vital for preventing complications and improving outcomes in polycystic liver disease. Abstract Polycystic liver disease is an uncommon genetic condition characterized
Faten Limaiem, Mohamed Hajri
doaj   +2 more sources

Isolated Polycystic Liver Disease

Acta Médica Portuguesa, 2017
N/A.
Rita Seara Costa, Bruno Gonçalves, Ana Isabel Rebelo   +2 more
doaj   +3 more sources

Modelling polycystic liver disease progression using age-adjusted liver volumes and targeted mutational analysis [PDF]

JHEP Reports, 2022
Background & Aims: Polycystic liver disease (PLD) manifests as numerous fluid-filled cysts scattered throughout the liver parenchyma. PLD most commonly develops in females, either as an extra-renal manifestation of autosomal-dominant polycystic ...
Dana Sierks, Ria Schönauer, Anja Friedrich, Elena Hantmann, Jonathan de Fallois, Nikolas Linder, Janett Fischer, Adam Herber, Carsten Bergmann, Thomas Berg, Jan Halbritter   +10 more
doaj   +2 more sources

Polycystic Liver Disease – Something to Consider in Case of an Acute Abdomen [PDF]

Iberoamerican Journal of Medicine, 2021
Serghei Covantev, Rasul Uzdenov, Olga Belic   +2 more
doaj   +2 more sources

Management of Polycystic Liver Disease [PDF]

Canadian Journal of Gastroenterology, 2004
Polycystic liver disease (PCLD) is characterized by multiple cysts throughout the liver. Patients may develop chronic intractable symptoms that may be debilitating. Others may develop medical complications that necessitate intervention.
Justin Cheung, Charles H Scudamore, Eric M Yoshida   +2 more
doaj   +3 more sources

Clinical manifestation, epidemiology, genetic basis, potential molecular targets, and current treatment of polycystic liver disease [PDF]

Orphanet Journal of Rare Diseases
Polycystic liver disease (PLD) is a rare condition observed in three genetic diseases, including autosomal dominant polycystic liver disease (ADPLD), autosomal dominant polycystic kidney disease (ADPKD), and autosomal recessive polycystic kidney disease (
Amir Ali Mahboobipour, Moein Ala, Javad Safdari Lord, Arash Yaghoobi   +3 more
doaj   +2 more sources