Cystic fibrosis

Cystic fibrosis (CF) is a genetic disorder characterized by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity.

Pancreatitis

The presence of inflammation in the pancreas.


Total: 36

                       


(per page)
PMID (PMCID)
26546567
 FEMALE Child
Candida albicans pancreatitis in a child with cystic fibrosis post lung transplantation.
Hammer MM, Zhang L, Stoll JM, Sheybani EF.
Pediatr Radiol. 2016;46(4):575-8.
Candida albicans pancreatitis in a child with cystic fibrosis post lung transplantation.
26282838
 MALE Young Adult
Tigecycline-induced acute pancreatitis in a cystic fibrosis patient: A case report and literature review.
Hemphill MT, Jones KR.
J Cyst Fibros. 2016;15(1):e9-11.
The unique aspects of the case are highlighted, including the particular risk of drug-associated pancreatitis in those with cystic fibrosis.
24413785
 MIXED_SAMPLE
Chronic pancreatitis associated with the p.G208A variant of PRSS1 gene in a European patient.
Hegyi E, Cierna I, Vavrova L, Ilencikova D, Konecny M, Kovacs L.
JOP. 2014;15(1):49-52.
Mutations in the cationic trypsinogen gene (PRSS1) cause hereditary pancreatitis, while mutations in serine protease inhibitor Kazal type 1 (SPINK1), cystic fibrosis transmembrane conductance regulator (CFTR) and chymotrypsin C (CTRC) genes have been shown to associate with chronic pancreatitis as independent risk factors.
23949094
 MALE Infant, Newborn
False negative newborn screen and neonatal cholestasis in a premature child with cystic fibrosis.
Heidendael JF, Tabbers MM, De Vreede I.
Eur J Pediatr. 2014;173(12):1581-3.
In this case, the immunoreactive trypsinogen/pancreatitis-associated protein/35 cystic fibrosis transmembrane regulator mutation analysis/sequencing method was used.
23883480
(3750286)
 OTHER
Early acute pancreatitis in a child with compound heterozygosis ∆F508/R1438W/Y1032C cystic fibrosis: a case report.
Leonardi S, Pratico AD, Rotolo N, Di Dio G, Lionetti E, La Rosa M.
J Med Case Rep. 2013;7:188.
Recent studies suggest an important role of the cystic fibrosis transmembrane conductance regulator gene in the development of pancreatitis.
23883480
(3750286)
 OTHER
Early acute pancreatitis in a child with compound heterozygosis ∆F508/R1438W/Y1032C cystic fibrosis: a case report.
Leonardi S, Pratico AD, Rotolo N, Di Dio G, Lionetti E, La Rosa M.
J Med Case Rep. 2013;7:188.
The genotype-phenotype correlation in pancreatitis is rare compared to other organ manifestations, since this is seen almost exclusively among pancreatic sufficient patients with cystic fibrosis.
21673536
 FEMALE Adult
A novel exon duplication of the cystic fibrosis transmembrane conductance regulator in a patient presenting with adult-onset recurrent pancreatitis.
Kopp BT, Pastore MT, Sturm AC, Holtzlander MJ, Westman JA.
Pancreas. 2011;40(5):773-7.
Pancreatitis is a rare occurrence in patients with cystic fibrosis (CF) affecting 1.2% of all patients, but it can be the first presenting sign in approximately 15% of adults with pancreatic sufficiency and a milder CF phenotype.
17575549
 FEMALE Adult
Association of pancreas divisum and recurrent acute pancreatitis with the IVS8-5T-12TG allele of the CFTR gene and CFTR dysfunction.
Dray X, Fajac I, Bienvenu T, Chryssostalis A, Sogni P, Hubert D.
Pancreas. 2007;35(1):90-3.
Mild mutations or variants of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, including the IVS8-5T variant, are associated with idiopathic pancreatitis, but their relationship with PD is unknown.
14513373
 MALE Child
Transient exocrine pancreatic insufficiency as a possible complication of an enterovirus infection.
Van Biervliet S, De Waele K, Van Winckel M, Robberecht E.
Eur J Pediatr. 2003;162(12):872-4.
Exocrine pancreatic insufficiency is an exceptional problem in children, mostly associated with diseases like cystic fibrosis, Shwachman-Diamond syndrome or chronic pancreatitis, as is the case in idiopathic fibrosing pancreatitis.
12422349
 MALE Adult
Cystic fibrosis presenting as acute pancreatitis and obstructive azoospermia in a young adult male with a novel mutation in the CFTR gene.
Conway SP, Peckham DG, Chu CE, Ellis LA, Ahmed M, Taylor GR.
Pediatr Pulmonol. 2002;34(6):491-5.
Patients with cystic fibrosis and unexplained upper abdominal pain should be screened for pancreatitis, and consideration should be given to screening patients with idiopathic pancreatitis for mutations in the CFTR gene.
12422349
 MALE Adult
Cystic fibrosis presenting as acute pancreatitis and obstructive azoospermia in a young adult male with a novel mutation in the CFTR gene.
Conway SP, Peckham DG, Chu CE, Ellis LA, Ahmed M, Taylor GR.
Pediatr Pulmonol. 2002;34(6):491-5.
Patients with cystic fibrosis and unexplained upper abdominal pain should be screened for pancreatitis, and consideration should be given to screening patients with idiopathic pancreatitis for mutations in the CFTR gene.
11296204
 FEMALE Adult
Minocycline-induced pancreatitis in cystic fibrosis.
Boyle MP.
Chest. 2001;119(4):1283-5.
Minocycline-induced pancreatitis in cystic fibrosis.
11446679
 MALE Adult
The spectrum of CFTR-related disease.
Boyle MP.
Intern Med. 2001;40(6):522-5.
This case describes a patient with documented CFTR dysfunction by nasal potential difference measurement who presents with chronic idiopathic pancreatitis, sinusitis, and allergic bronchopulmonary aspergillosis (ABPA), but not congenital bilateral absence of the vas deferens (CBAVD) or other classic symptoms of cystic fibrosis.
11100529
 MALE Child
Recurrent pancreatitis secondary to type V hyperlipidemia: report of one case.
Chen HH, Lin LH.
Acta Paediatr Taiwan. 2000;41(5):276-8.
With the exception of cystic fibrosis and hereditary pancreatitis, case reports about pancreatitis in children have rarely been mentioned.
11100529
 MALE Child
Recurrent pancreatitis secondary to type V hyperlipidemia: report of one case.
Chen HH, Lin LH.
Acta Paediatr Taiwan. 2000;41(5):276-8.
With the exception of cystic fibrosis and hereditary pancreatitis, case reports about pancreatitis in children have rarely been mentioned.
10533146
 FEMALE Adult
[Acute pancreatitis revealing cystic fibrosis in an adult].
Dray X, Zinzindohoue F, Cuillerier E, Cugnenc PH, Barbier JP, Marteau P.
Gastroenterol Clin Biol. 1999;23(8-9):974-7.
This exceptional case shows that cystic fibrosis should be suspected in each case of idiopathic pancreatitis.
9893301
 MIXED_SAMPLE Child
Hereditary pancreatitis: report of a family from Turkey.
Kansu A, Girgin N, Yurdaydin C, Cetinkaya H, Uzunalimoglu O.
Acta Paediatr Jpn. 1998;40(6):612-5.
Chronic pancreatitis is a rare disease in children and is usually secondary to underlying diseases such as hereditary pancreatitis, cystic fibrosis, hyperlipidemia, prolonged malnutrition, gallstones or anomalies of the biliary-pancreatic duct system.
7776104
 MALE
Chronic pancreatitis in a patient with cystic fibrosis and clinical pancreatic insufficiency.
del Rosario JF, Putnam PE, Orenstein DM.
J Pediatr. 1995;126(6):951-2.
We describe a patient with homozygous delta F508 cystic fibrosis and typical symptoms of pancreatic insufficiency (greasy, fatty stools) in whom pancreatitis developed.
1578312
 FEMALE Child
Pancreatitis in young children with cystic fibrosis.
Atlas AB, Orenstein SR, Orenstein DM.
J Pediatr. 1992;120(5):756-9.
In one patient pancreatitis was diagnosed before cystic fibrosis and diagnosis of cystic fibrosis was delayed.
1578312
 FEMALE Child
Pancreatitis in young children with cystic fibrosis.
Atlas AB, Orenstein SR, Orenstein DM.
J Pediatr. 1992;120(5):756-9.
In one patient pancreatitis was diagnosed before cystic fibrosis and diagnosis of cystic fibrosis was delayed.