Chapter 26 - The Pediatric Abdomen Flashcards
describes the absence or deficiency of bile secretion or failure of the bile to enter the alimentary tract (i.e., secondary to obstruction); the stool is claylike and colorless
Acholic
inflammation of the appendix
appendicitis
fecalith or calcification located within the appendix; echogenic
appendicolith
congenital absence or closure of a normal body opening or tubular structure
atretic
hereditary disorder transmitted as an autosomal recessive trait; clinical manifestations include umbilical hernia (exomphalos), macroglossia, and gigantism, often accompanied by visceromegaly and dysplasia of the renal medulla; also called exophthalmos-macroglossia-gigantism (EMG) syndrome
Beckwith-Wiedemann syndrome
closure or absence of some or all of the major bile ducts
biliary atresia
congenital cystic malformation of the common bile duct
choledochal cyst
excessive development of one side or one half of the body or an organ
hemihypertrophy
thickened muscle in the pylorus that prevents food from entering the duodenum; occurs more frequently in males
hypertrophic pyloric stenosis (HPS)
thickened by absorption, evaporation, or dehydration
inspissated
occurs when bowel prolapses into distal bowel and is propelled in an antegrade fashion
intussusception
infant in the first 28 days of life
neonate
(Wilms’ tumor) a rapidly developing tumor of the kidney that usually occurs in children
nephroblastoma
a malignant hemorrhagic tumor principally consisting of cells resembling neuroblasts that give rise to cells of the sympathetic system (especially the adrenal medulla)
neuroblastoma
condition in pyloric stenosis in the neonatal period; after drinking, the infant experiences projectile vomiting secondary to the obstruction in the pylorus
projectile vomiting