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Pancreas hypoplasia

Annular pancreas, pancreas divisum, pancreatic hypoplasia and agenesis, heterotopic pancreas Inherited syndromes affecting the pancreas Cystic fibrosis... [Pg.1867]

Mature cartilage or bone lungs kidneys liver pancreas adrenal gland pituitary gland Fairly low Hypoplasia secondary damage to the fine vasculature and connective tissue elements... [Pg.47]

Complete agenesis of the pancreas is usually incompatible with life. Therefore, pancreatic aplasia or hypoplasia is uncommon in humans. Patients with pancreatic hypoplasia will have a normal development of the pancreas in size and shape but later in life will have a replacement of the glandular elements with fatty tissue. Some of these patients will present with an abnormal exocrine pancreatic insufficiency and normal endocrine function. Children with syndromes such as Schwachman-Diamond, Beckwith-Wiedemann, polysplenia bilobed lungs, and congenital heart disease have a higher relative risk of hypoplasia of the pancreas (Gazelle et al. 1998). [Pg.157]

The characteristic CT findings of intestinal nonrotation include abnormal orientation of the superior mesenteric vessels, aplasia or hypoplasia of the uncinate process of the pancreas, right-sided small bowel loops, a left-sided colon, and the absence of the horizontal part of the duodenum. Vertical or reversed location of the superior mesenteric vessels is, however, not specific for intestinal malrotation. [Pg.169]


See other pages where Pancreas hypoplasia is mentioned: [Pg.39]   
See also in sourсe #XX -- [ Pg.157 ]




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