Zobrazeno 1 - 10
of 1 387
pro vyhledávání: '"Liver cysts"'
Autor:
Faten Limaiem, Mohamed Hajri
Publikováno v:
Clinical Case Reports, Vol 12, Iss 5, Pp n/a-n/a (2024)
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 character
Externí odkaz:
https://doaj.org/article/1938813f5f2d4f7683e909cf0454265a
Autor:
Joonho Jeong, Hyun Joon Park
Publikováno v:
Kosin Medical Journal, Vol 38, Iss 2, Pp 75-86 (2023)
Polycystic liver disease (PLD) is a hereditary disease characterized by the presence of 20 or more liver cysts. It is classified into three types: isolated autosomal dominant PLD, PLD with autosomal dominant polycystic kidney disease, and PLD with au
Externí odkaz:
https://doaj.org/article/cd69757a0c8c47afb67e132430ea778c
Autor:
Norcia LF, Watanabe EM, Hamamoto Filho PT, Hasimoto CN, Pelafsky L, de Oliveira WK, Sassaki LY
Publikováno v:
Hepatic Medicine: Evidence and Research, Vol Volume 14, Pp 135-161 (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, B
Externí odkaz:
https://doaj.org/article/2e277ed29891486db65e99993a800ef8
Autor:
Jonas Buttenschoen, Vlad Pavel, Alexander Mehrl, Bernhard Michels, Sheila Albaladejo Fuertes, Bettina Seydel, Sophie Schlosser-Hupf, Martina Müller, Stephan Schmid
Publikováno v:
Medicina, Vol 59, Iss 10, p 1828 (2023)
Background and Objectives: Alveolar echinococcosis (AE) is a highly variable disease able to present as structurally diverse cysts in different organs based on the host’s immunological state as well as the time between diagnosis and the primary inf
Externí odkaz:
https://doaj.org/article/c7025df1a6054a6d83ba43b252928bb4
Autor:
Carola Buscemi, Cristiana Randazzo, Paolo Buscemi, Rosalia Caldarella, Martina Lombardo, Silvio Buscemi
Publikováno v:
Tropical Medicine and Infectious Disease, Vol 8, Iss 9, p 449 (2023)
Cystic echinococcosis is a zoonosis caused by the ingestion of food or water contaminated by Echinococcus eggs. E. granulosus is the most common causative agent of cystic echinococcosis that still has a relevant incidence in Italy, especially on the
Externí odkaz:
https://doaj.org/article/c1641bb9b30c4856b8fb054d984b7a7e
Autor:
Sho Ishikawa, Shintaro Kuroda, Keigo Chosa, Kenjiro Okada, Naoki Tanimine, Hiroyuki Tahara, Masahiro Ohira, Kentaro Ide, Tsuyoshi Kobayashi, Hideki Ohdan
Publikováno v:
Surgical Case Reports, Vol 7, Iss 1, Pp 1-7 (2021)
Abstract Background Liver cysts are common, with most cases being asymptomatic. In symptomatic cases, the disease is amenable to treatment. However, huge or multiple liver cysts with vascular narrowing and associated systemic symptoms are extremely r
Externí odkaz:
https://doaj.org/article/003026de8d7f42ad87f9696b3e53fb97
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Autosomal dominant polycystic kidney disease (ADPKD) is the most commonly inherited kidney disease and is associated with cystic manifestation in the liver. Patients with ADPKD are at higher risk for hernias, here we present an image of an i
Externí odkaz:
https://doaj.org/article/579b3ee2ce714e088bbf847c5d651132
Autor:
Liyanne F. M. van de Laarschot, René H. M. te Morsche, Alexander Hoischen, Hanka Venselaar, Hennie M. Roelofs, Wybrich R. Cnossen, Jesus M. Banales, Ronald Roepman, Joost P. H. Drenth
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Polycystic liver disease (PLD) is an inherited disorder characterized by numerous cysts in the liver. Autosomal dominant polycystic kidney and liver disease (ADPKD and ADPLD, respectively) have been linked to pathogenic GANAB vari
Externí odkaz:
https://doaj.org/article/c710959f5f25452a936f4f4f95599345
Autor:
Bianca Santana de Cecco, Marina Paula Lorenzett, Luan Cleber Henker, Juliana Bisol, Aline Girotto Soares, Anelise Bonilha Trindade-Gerardi, Marcelo Meller Alievi, Luciana Sonne
Publikováno v:
Ciência Rural, Vol 52, Iss 9 (2022)
ABSTRACT: Caroli syndrome is characterized by a combination of intrahepatic biliary ductal ectasia and congenital ductal fibrosis due to the failure of involution of ductal plates and large intrahepatic ducts. This study aims to report Caroli syndrom
Externí odkaz:
https://doaj.org/article/10d11c5edb034ef5b08bc9a62266d3c7
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