Cystic duct

You’re the Expert: Cystic Fibrosis Cystic fibrosis is an inherited genetic disease that currently affects approximately 30,000 Americans and 70,000 people worldwide. The isolated gene malformation affects the exocrine glands that results in alterations in the physiologic functioning of the respiratory, gastrointestinal, and reproductive systems (Ball and Bindler, 2014). The name cystic fibrosis refers to the characteristic cysts and fibrosis that occurs within the pancreas. It is the most common

Cystic Fibrosis Case Commentary Cystic fibrosis (CF) is an autosomal recessively inherited condition that affects approximately 9000 patients in the UK (Rowe et al, 2005). CF is caused by a mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene (Rowe et al, 2005), resulting in deficiencies in normal ion transport across cell membranes (Mall and Boucher, 2014). Abnormal ion transport causes the sputum to become dehydrated and more viscous (Mall and Boucher, 2014), leading

Cystic Fibrosis Nicholas Culver Introduction Cystic fibrosis is an inherited disease. It’s very common In the United States. It’s also very common amongst the Caucasian population. Its effects 1 in every 3,000 new born babies. Cystic fibrosis is less common in other ethnic groups. Effecting 1 in every 17,000 African Americans and 1 in every 30,000 Asian Americans. It causes the body to make a very thick type of mucus. The mucus is caused by an unbalance in salt in a person’s body. Leaving few

psychosocial affects of cystic fibrosis in adolescents Cystic fibrosis (CF) is a progressive condition in which epithelial exocrine glands are obstructed (Howe, 2001). Whilst many organs and bodily systems are disrupted by CF, the lungs and gastrointestinal organs are predominantly affected; it is also most common amongst the Caucasian population due to the autosomal recessive gene (Quitter et al., 2003 cited in Wolfe & Mash, 2006, pg 514). The faulty gene effects the production of cystic fibrosis transmembrane

In light of question number three A-B, Cystic fibrosis causes variations from the norm in almost all exocrine and numerous endocrine organs. This disturbance of organs extremely thwarts the elements of the Pancreas during absorption bringing about “…an abnormal mucous secretion that causes obstruction of single mucin-producing cells. The pancreas secretes less enzyme (ex: trypsin, lipase and amylase), so malabsorption ensues with its attendant deficiency disorders” (Walsh et al.) While Sam's stomach

non-inflammatory cystic lesions of the pancreas. Utilization of the International Consensus Guidelines for the diagnosis and treatment of IPMN and MCN assist physicians in the management of these cystic lesions while proving the highest quality of care. Introduction Intraductal Papillary Mucinous Neoplasms (IPMN) are tumors that grow within the pancreatic duct that produce thick fluid. This tumor can be classified as main duct IPMN or branch duct IPMN. The classification between main duct IPMN and branch

the gastrointestinal tract. The second is the hepatic artery, which carries oxygen rich blood to the liver from the heart and lungs. There are two major structures that leave the liver, the hepatic vein and the bile duct. The hepatic vein takes the blood from the liver, while the bile duct takes bile to the gall bladder. The liver is a storage place for glucose and production of urea from amino groups and ammonia. It stores many essential

the area due to a gallstone blocking the cystic duct (Schaider, Barkin and Barkin, 2015). A gallbladder is an organ that is located below the liver. Its primary function is to store bile, which the body uses to digest fat in the small intestines. When the bile becomes too concentrated, it begins to form insoluble minerals and salt and these deposits are called gallstones. Small gallstones do not cause any problems if they can be flushed down the bile duct and

remaining 10-15% of pancreatic tumors are a heterogeneous group of pancreatic neoplasms that includes cystic pancreatic neoplasms, endocrine tumors and other uncommon pancreatic tumors. Magnetic resonance imaging (MRI) is reliable for the characterization of solid and cystic pancreatic lesions. Due to the excellent soft tissue contrast, MRI is able to readily separate cystic from noncystic tumors. Cystic tumors are frequently easier to diagnose since they often possess typical imaging findings that permit

management difficulty (Lau and Eric, 2008). ERCP-associated perforations of the esophagus, stomach or duodenum distant from the ampulla are all caused by the endoscope. Peri-ampullary retroperitoneal perforations usually are caused by ES or result from bile duct injuries related to instrumentation with a wire or basket (Suissa et al, 2005). Perforations can be classified into four types: Type I: lateral or medial duodenal wall perforation, Type II: peri- Vaterian injuries, Type