Necrotizing pancreatitis as an atypical presentation of cystic fibrosis in a preschool patient
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Abstract
Background: Cystic fibrosis is a disease with autosomal recessive inheritance, consisting of mutations in the transmembrane conductivity regulatory gene, causing an alteration in the viscosity of secretions. Case report: We present the case of a preschool patient admitted due to chronic abdominal pain who was diagnosed with necrotizing pancreatitis as a cystic fibrosis debut, requiring four months of hospitalization. Conclusion: Cystic fibrosis is a disease with a high morbidity and mortality rate in the pediatric population; physicians should know its possible debut forms and clinical presentation for timely management and interdisciplinary follow-up.
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References
Navarro S. Recopilación histórica de la fibrosis quística. Gastroenterol Hepatol. 2015.
Sojo A, Martínez N, Bousoño C, García M, Heredia S, Mazanares J, et al. Pancreatitis en la fibrosis quística: correlación con el genotipo y estado pancreático. An Pedatr. 2011;75(6):401-8.
Santana E, Tamayo V, Collazo T, López I, Feria F, Rodríguez F. Caracterización clínica y genética de la fibrosis quística en la provincia de Holguín. Rev Cuba Pediatr. 2017;89(2):136–44.
Restrepo-Gualteros S, Milena S, Muñoz A, Quevedo J. Complicaciones pulmonares en fibrosis quística. Reper Med Cir. 2016;25(1):22–32.
Delgado I, Moreno M, Carrasco L, Marín L, Muñoz P, Moreno M, et al. Atelectasia persistente en paciente con fibrosis quística: ¿debemos tratarla siempre con antibioterapia? Arch Bronconeumol. 2019;55(1):54–5.
Ruiz de Valbuena M. Fibrosis quística y sus manifestaciones respiratorias. Pediatr Integr. 2016;XX(2):119–27.
Guarner L. Fisiopatología , diagnóstico y tratamiento de la insuficiencia pancreática exocrina en el paciente con fibrosis quística. Gastroenterol Hepatol. 2005;28(Supl 2):29–32.
Ledesma S, Álvarez A, Torres M, de Gracia J. Pancreatitis aguda como forma de presentación de una fibrosis quística. Med Clin. 2003;120(10):399.
Villamañán A, de Vicente C, García R. Pancreatitis aguda secundaria a Campylobacter jejuni en un niño afecto de fibrosis quística. Med Clin. 2017.
Foruny J, Moreira V, Maiz L, Carrera E, Casals T. Pancreatitis aguda recidivante como forma de presentación de fibrosis quística. Gastroenterol Hepatol. 2005;28(1):20–2.