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Quoted phrase not found in phrase index: "Malformation of the hepatic ductal plate"
Page 1
Jaundice revisited: recent advances in the diagnosis and treatment of inherited cholestatic liver diseases.
Chen HL, Wu SH, Hsu SH, Liou BY, Chen HL, Chang MH. Chen HL, et al. J Biomed Sci. 2018 Oct 26;25(1):75. doi: 10.1186/s12929-018-0475-8. J Biomed Sci. 2018. PMID: 30367658 Free PMC article. Review.
DCDC2 is a newly identified genetic disorder causing neonatal sclerosing cholangitis. Other cholestatic genetic disorders may have extra-hepatic manifestations, such as developmental disorders causing ductal plate malformation (Alagille syndrome, polyc …
DCDC2 is a newly identified genetic disorder causing neonatal sclerosing cholangitis. Other cholestatic genetic disorders may have extra- …
Congenital hepatic fibrosis: case report and review of literature.
Hasbaoui BE, Rifai Z, Saghir S, Ayad A, Lamalmi N, Abilkassem R, Agadr A. Hasbaoui BE, et al. Pan Afr Med J. 2021 Feb 18;38:188. doi: 10.11604/pamj.2021.38.188.27941. eCollection 2021. Pan Afr Med J. 2021. PMID: 33995794 Free PMC article. Review.
Congenital hepatic fibrosis (CHF) is a rare autosomal recessive disease derived from biliary dysgenesis secondary to ductal plate malformation; it often coexists with Caroli's disease, von Meyenburg complexes, autosomal dominant polycystic kidne …
Congenital hepatic fibrosis (CHF) is a rare autosomal recessive disease derived from biliary dysgenesis secondary to ductal …
An update on ductal plate malformations and fibropolycystic diseases of the liver.
Mirza H, Besse W, Somlo S, Weinreb J, Kenney B, Jain D. Mirza H, et al. Hum Pathol. 2023 Feb;132:102-113. doi: 10.1016/j.humpath.2022.06.022. Epub 2022 Jun 28. Hum Pathol. 2023. PMID: 35777701 Review.
A variety of cystic and fibrocystic lesions can occur in the liver, which may be single or multiple and etiologically can be acquired or have genetic underpinnings. Although the morphology of ductal plate development and various associated malformations has b …
A variety of cystic and fibrocystic lesions can occur in the liver, which may be single or multiple and etiologically can be acquired or hav …
Hepatic Cysts: Reappraisal of the Classification, Terminology, Differential Diagnosis, and Clinicopathologic Characteristics in 258 Cases.
Armutlu A, Quigley B, Choi H, Basturk O, Akkas G, Pehlivanoglu B, Memis B, Jang KT, Erkan M, Erkan B, Balci S, Saka B, Bagci P, Farris AB, Kooby DA, Martin D, Kalb B, Maithel SK, Sarmiento J, Reid MD, Adsay NV. Armutlu A, et al. Am J Surg Pathol. 2022 Sep 1;46(9):1219-1233. doi: 10.1097/PAS.0000000000001930. Epub 2022 Jul 4. Am J Surg Pathol. 2022. PMID: 35778790
Two hundred and fifty-eight 1 cm cysts evaluated pathologically using updated criteria were classifiable as: I. Ductal plate malformation related (63%); that is, cystic bile duct hamartoma or not otherwise specified-type benign biliary cyst (35 with polycysti …
Two hundred and fifty-eight 1 cm cysts evaluated pathologically using updated criteria were classifiable as: I. Ductal plate …
Congenital Cystic Lesions of the Bile Ducts: Imaging-Based Diagnosis.
Cannella R, Giambelluca D, Diamarco M, Caruana G, Cutaia G, Midiri M, Salvaggio G. Cannella R, et al. Curr Probl Diagn Radiol. 2020 Jul-Aug;49(4):285-293. doi: 10.1067/j.cpradiol.2019.04.005. Epub 2019 Apr 6. Curr Probl Diagn Radiol. 2020. PMID: 31027922 Review.
Congenital cystic lesions of the bile ducts represent a spectrum of liver and biliary system lesions, resulting from abnormal embryologic development of the ductal plate. These disorders include Caroli disease, choledochal cysts, autosomal dominant polycystic …
Congenital cystic lesions of the bile ducts represent a spectrum of liver and biliary system lesions, resulting from abnormal embryol …
Pediatric Hepatic Cystic Lesions: Differential Diagnosis and Multimodality Imaging Approach.
Riedesel EL, Richer EJ, Taylor SD, Tao T, Gagnon MH, Braithwaite KA, Alazraki AL, Khanna G. Riedesel EL, et al. Radiographics. 2022 Sep-Oct;42(5):1514-1531. doi: 10.1148/rg.220006. Epub 2022 Jul 15. Radiographics. 2022. PMID: 35839138
The location of a cystic lesion and its number, size, composition, and relationship to the biliary system are features that help in narrowing the differential diagnosis. An incidentally detected simple hepatic cyst is the most commonly encountered. Ciliated foregut cysts a …
The location of a cystic lesion and its number, size, composition, and relationship to the biliary system are features that help in narrowin …
Imaging features of ductal plate malformations in adults.
Venkatanarasimha N, Thomas R, Armstrong EM, Shirley JF, Fox BM, Jackson SA. Venkatanarasimha N, et al. Clin Radiol. 2011 Nov;66(11):1086-93. doi: 10.1016/j.crad.2011.05.008. Epub 2011 Aug 15. Clin Radiol. 2011. PMID: 21840516 Review.
Ductal plate malformations, also known as fibrocystic liver diseases, are a group of congenital disorders resulting from abnormal embryogenesis of the biliary ductal system. ...Accurate diagnosis of ductal plate malformations …
Ductal plate malformations, also known as fibrocystic liver diseases, are a group of congenital disorders result …
The Ductal Plate From the Inside Out: An Illustrated Review of Fibropolycystic Liver Disease.
Kinoshita IHB, Torres US, Zanini LAP, Pinto MF, Veloso JCV, de Siqueira GRS, D'Ippolito G. Kinoshita IHB, et al. Semin Ultrasound CT MR. 2022 Dec;43(6):510-516. doi: 10.1053/j.sult.2022.06.008. Epub 2022 Jun 10. Semin Ultrasound CT MR. 2022. PMID: 36462809
Fibropolycystic liver disease is a continuum of disorders that result from insults to the ductal plate at different stages of development and are often associated with each other. Caroli's syndrome, polycystic liver disease, biliary hamartomas, and congenital …
Fibropolycystic liver disease is a continuum of disorders that result from insults to the ductal plate at different stages of …
Biliary atresia revisited.
Kahn E. Kahn E. Pediatr Dev Pathol. 2004 Mar-Apr;7(2):109-24. doi: 10.1007/s10024-003-0307-y. Epub 2004 Mar 4. Pediatr Dev Pathol. 2004. PMID: 14994122 Review.
The symptoms of the former start shortly after birth and there is frequently an association with a variety of congenital anomalies. Children with the perinatal form become jaundiced several weeks after birth; no associated congenital anomalies are present. ...The di …
The symptoms of the former start shortly after birth and there is frequently an association with a variety of congenital anomalies. C …
Diagnosis and management of polycystic liver disease.
Gevers TJ, Drenth JP. Gevers TJ, et al. Nat Rev Gastroenterol Hepatol. 2013 Feb;10(2):101-8. doi: 10.1038/nrgastro.2012.254. Epub 2013 Jan 8. Nat Rev Gastroenterol Hepatol. 2013. PMID: 23296249 Review.
The condition is associated with two genetically distinct diseases: as a primary phenotype in isolated polycystic liver disease (PCLD) and as an extrarenal manifestation in autosomal dominant polycystic kidney disease (ADPKD). Processes involved in hepatic cystogenesis inc …
The condition is associated with two genetically distinct diseases: as a primary phenotype in isolated polycystic liver disease (PCLD) and a …
55 results