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About 275 results

ALLMedicine™ Hepatic Cysts Center

Research & Reviews  107 results

AN 8-YEAR-OLD CALIFORNIA GIRL WITH ASYMPTOMATIC HEPATIC CYSTS.
https://doi.org/10.1097/INF.0000000000003539
The Pediatric Infectious Disease Journal; Passarelli P, Ramchandar N et. al.

Apr 15th, 2022 - Echinococcus infections are rare in the United States but may present a growing public health threat. We present the case of an 8-year-old female patient from Southern California who was diagnosed with hepatic echinococcosis after the incidental d...

An unusual etiology of obstructive shock in the emergency department.
https://doi.org/10.1016/j.ajem.2022.01.014
The American Journal of Emergency Medicine; Murphy MP, Warren HR et. al.

Feb 2nd, 2022 - Obstructive shock describes any disease process that causes physical obstruction to blood flow into or out of the heart which results in impaired systemic oxygen or nutrient delivery. Common etiologies include cardiac tamponade, tension pneumothor...

Autophagy promotes hepatic cystogenesis in polycystic liver disease by depletion of cho...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035076
Hepatology (Baltimore, Md.); Masyuk AI, Masyuk TV et. al.

Dec 24th, 2021 - Polycystic liver disease (PLD) is characterized by defective cholangiocyte cilia that regulate progressive growth of hepatic cysts. Because formation of primary cilia is influenced by autophagy through degradation of proteins involved in ciliogene...

Polycystic Liver Disease: Advances in Understanding and Treatment.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842879
Annual Review of Pathology; Masyuk TV, Masyuk AI et. al.

Nov 2nd, 2021 - Polycystic liver disease (PLD) is a group of genetic disorders characterized by progressive development of cholangiocyte-derived fluid-filled hepatic cysts. PLD is the most common manifestation of autosomal dominant and autosomal recessive polycys...

Polycystic liver disease with lethal abdominal wall rupture: a case report.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330095
Journal of Medical Case Reports; Akuzawa D, Uchida Y et. al.

Aug 4th, 2021 - 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. Dialysis therapy can be used for renal failure, but liver transplantation...

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Clinicaltrials.gov  1 results

Penetration of Cefazolin Into Hepatic Cysts
https://clinicaltrials.gov/ct2/show/NCT02368015

Feb 3rd, 2016 - Hepatic cysts are fluid-filled cavities located in the liver parenchyma. They are usually asymptomatic, but can cause mass-related symptoms as abdominal pain, dyspnea and nausea. Aspiration sclerotherapy is indicated in patients with a dominant he...

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News  2 results

Autosomal dominant polycystic kidney disease and the heart and brain
https://www.mdedge.com/ccjm/article/139220/cardiology/autosomal-dominant-polycystic-kidney-disease-and-heart-and-brain?channel=194
Vinod Krishnappa, MBBS, Poornima Vinod, MD et. al.

Jun 1st, 2017 - Autosomal dominant polycystic kidney disease (ADPKD) has significant extrarenal manifestations. Hypertension is a common complication, arises early in the course of the disease, and is implicated in the development of left ventricular hypertrophy.

An 18-year-old woman with hepatic cysts
https://www.mdedge.com/ccjm/article/96075/imaging/18-year-old-woman-hepatic-cysts?channel=162
Cynthia H. Ho, MD, Jamie Lin, MD

May 1st, 2014 - An 18-year-old woman presents with 3 days of epigastric abdominal pain, with no fever or constitutional symptoms. She was born in the United States and reports yearly trips since age 3 to her family’s farm in a rural area of Mexico, where she is e.

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