Acute Liver Failure in Children
Fig. 70.1 Pathogenesis of liver cell injury is multifactorial with several factors influencing liver cell death and regeneration. When the net result is liver cell loss beyond a critical mass…
Fig. 70.1 Pathogenesis of liver cell injury is multifactorial with several factors influencing liver cell death and regeneration. When the net result is liver cell loss beyond a critical mass…
Fig. 53.1 Liver haematopoiesis A caudal part of the liver bud becomes the gallbladder and its stalk, the cystic duct [7]. The intrahepatic bile ducts develop from the limiting plates…
Fig. 36.1 Pathophysiological mechanisms of congenital disorders of intestinal electrolytes transport. 1 Familial diarrhea syndrome is due to a mutation in intestinal guanylate cyclase receptor (GC-C) for the endogenous ligands…
Biliary excretion is the only mechanism for copper elimination under physiological conditions, and it increases with increasing size of the hepatic copper pool. Trafficking of copper in and through the…
Fig. 33.1 Early acute pancreatitis. Note edematous gland (black arrow) with a small amount of fluid (small arrow). No visible ducts or calcifications. (Images courtesy of Dr. David Gregg) Pathophysiology…
All anatomical areas Giardiasis Granulation tissue polyps Inflammatory bowel disease Lymphangiectasia Lymphoma Multiple adenomatous or hyperplastic polyps Metastatic tumours Familial and sporadic gastrointestinal polyposes Ganglioneuromatosis Neuroendocrine hyperplasia and neoplasia Stomach …
Fig. 10.1 Pathophysiologic mechanisms for GER. (Reproduced from Ref. [29], with permission from John Wiley and Sons) GER occurs during episodes of TLESR or inadequate adaptation of the sphincter tone…
(1) Department of Translational Medical Sciences, Section of Pediatrics, University of Naples “Federico II”, Via S. Pansini 5, 80131 Naples, Italy Massimo Martinelli Email: staiano@unina.it KeywordsHirschsprung’s diseaseIntestinal neuronal dysplasiaRectal suction…
Fig. 46.1 Possible routes for EN EN is used to preserve nutritional status, support normal growth, and treat malnutrition when oral feeding is inadequate or not possible. EN is more…
Chagas disease Tumors (e.g., leiomyoma, Hodgkin’s disease, gastric carcinoma; “pseudoachalasia”) Sarcoidosis Hereditary cerebellar ataxia Eosinophilic esophagitis Hirschsprung’s disease Chronic idiopathic intestinal pseudo-obstruction Multiple endocrine neoplasia type 2b Miscellaneous (e.g., juvenile…