2016
DOI: 10.1007/s12098-016-2115-1
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Pancreatitis in Children

Abstract: Pancreatic disease in children has a wide clinical spectrum and may present as Acute pancreatitis (AP), Acute recurrent pancreatitis (ARP), Chronic pancreatitis (CP) and Pancreatic disease without pancreatitis. This article highlights the etiopathogenesis and management of pancreatitis in children along with clinical data from five tertiary care hospitals in south India [Chennai (3), Cochin and Pune].

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Cited by 18 publications
(16 citation statements)
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“…Pancreatitis exhibits a wide clinical spectrum in children and may present as AP, ARP or CP (8). AP is the most common pathological entity affecting the pancreas in children, and the diagnosis of AP is based on a combination of clinical findings, biochemical tests and imaging studies (10, 12) The two classical symptoms of AP are abdominal pain and nausea/vomiting.…”
Section: Discussionmentioning
confidence: 99%
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“…Pancreatitis exhibits a wide clinical spectrum in children and may present as AP, ARP or CP (8). AP is the most common pathological entity affecting the pancreas in children, and the diagnosis of AP is based on a combination of clinical findings, biochemical tests and imaging studies (10, 12) The two classical symptoms of AP are abdominal pain and nausea/vomiting.…”
Section: Discussionmentioning
confidence: 99%
“…It is well documented that mutations in the PRSS1, CFTR and SPINK1 genes can cause hereditary pancreatitis. However, there is no clear distinction between those diseases that cause recurrent attacks of AP and those causing CP (8). An evaluation of PRSS1, SPINK1 and CFTR mutations may be beneficial in children with a family history of ARP or CP.…”
Section: Discussionmentioning
confidence: 99%
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“…Hallazgos imagenológicos compatibles con pancreatitis aguda. 2,3 La incidencia de la pancreatitis aguda en la población pediátrica ha ido en aumento en Estados Unidos y es de 3,6-13,2 casos por 100 000 niños por año. 4,5 Son varias las causas de pancreatitis en niños; entre las de mayor frecuencia, se encuentran enfermedades sistémicas, como sepsis, shock, enfermedad inflamatoria intestinal, síndrome urémico hemolítico (10-50%); medicamentos, como ácido valproico, 6-mercaptopurina/azatioprina, l-asparaginasa, masalamina, trimetoprimasulfametoxazol, furosemida, tacrolimus, esteroides (5-25%); factores obstructivos: cálculos biliares, páncreas divisum, quistes en el colédoco, disfunción del esfínter de Oddi, páncreas anular (10-30%); trauma (10-20%); infección viral (8-10%); enfermedades metabólicas, como cetoacidosis diabética, hipertrigliceridemia, errores innatos del metabolismo e hipercalcemia (5-10%); y, finalmente, causas idiopáticas (15-30%).…”
Section: Niveles De Amilasa O Lipasa Tres Vecesunclassified
“…The article on BPancreatitis in children^addresses the entire spectrum of pancreatitis i.e., acute pancreatitis (AP), acute recurrent pancreatitis (ARP) and chronic pancreatitis (CP) [8]. It will help the reader in differentiation of various forms of pancreatitis, finding the etiology and providing state of the art management.…”
mentioning
confidence: 99%