CH 8 Pediatric Pancreas Flashcards

1
Q

Pancreas

A

retroperitoneal structure. functions as an endocrine and exocrine gland.

Endocrine function: secrete insulin via the islets of langerhans.

Exocrine function: secrete trypsin, lipase and amylase.

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2
Q

Pancreas location

A

Pancreas lies between the splenic hilum and the duodenal loop. the GDA is anterolateral to the pancreatic head and the CBD is posterolateral to the pancreatic head. The SMA/SMV are posterior to the neck of the pancreas and anterior to the uncinate process. the splenic artery courses along the superior border of the pancreas and the splenic vein is posterior.

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3
Q

Duct of Wirsung

A

main pancreatic duct.
courses through the pancreas and joins the CBD to form the ampulla of Vater which empties into the 2nd portion of the duodenum.

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4
Q

Duct of santorini

A

accessory pancreatic duct, empties into the duodenum, proximal to the ampulla of Vater.

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5
Q

*Pancreas divisum

A

occurs when the ventral and dorsal pancreatic buds do not fuse and each maintains a separate duct. This results in a smaller duct of santorini which may cause pancreatitis due to inadequate pancreatic enzyme drainage.

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6
Q

Pancreatic cysts

A

true pancreatic cysts are rare. They are associated with ADPKD, von hippel - lindau and cystic fibrosis.

congenital cysts of the pancreas are caused by anomalous development of the pancreatic ducts.

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7
Q

Annular pancreas

A

ventral segment of the developing pancrease encircles the duodenum and forms a ring of pancreatic tissue causing and obstruction of the gastric outlet. (2nd most common panc anomaly)

more common in males

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8
Q

Annular pancreas associated with congenital disorders:

A

Down’s syndrome, TEF (tracheoesophageal fistula), intestinal atresia and pancreas divisum.

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9
Q

Ectopic pancreas

A

lies in the submucosal position and occurs around the antrum of the stomach.

associated with: VATER syndrome, gut malrotation, and duodenal atresia.

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10
Q

Nesidioblastosis

A

persistence of the fetal state of the pancreas.
Nesidioblast secrete insulin.
babies present with HYPOglycemia

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11
Q

Effect of cystic fibrosis on pancreas

A

85% of children with cystic fibrosis have pancreatic insufficiency, which leads to steatorrhea (fat in feces) and malabsorption. Ducts become dilated and cause small cysts and fibrosis of pancreas.

*thickened mucus lines pancratic, bronchial, and biliary ducts.

obstruction and distention lead to: degeneration, atrophy, insufficiency, fibrosis, and fatty replacement.

Sono: increase in echogenicity and decrease in size

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12
Q

Schwachman syndrome:

A

causes: pancreatic insufficiency (2nd most common), and fatty infiltrate of pancreas.
sono: normal hyperechoic pancreas

Syndrome includes: metaphyseal chondroplasia (shortening of extremities), metaphyseal widening “cupping” of the ribs and bone marrow hypoplasia, enlarged spleen.

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13
Q

Acute pancreatitis

A

usually due to blunt abdominal trauma or non-accidental injury (child abuse)
can be caused by: mumps, drug toxicity and biliary and pancreatic anomalies.

sono: pancreas appears hypoechoic and edematous
* trauma due to child abuse is the most common cause in children.

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14
Q

Pancreatitis symptoms:

A

constant, severe epigastric or periumbilical pain which radiates to the back and shoulders nd the patient has raised amylase levels.

rest, and oral feedings must be stopped.

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15
Q

Chronic pancreatitis

A

repeated attacks of pancreatitis and is NOT reversible.

sono: pancreas usually small due to fibrosis and appears heterogeneous. calcifications may be present and dilatation of the pancreatic duct and CBD is common.

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16
Q

Causes of chronic pancreatitis in children:

A
autoimmune pancreatitis
hereditary pancreatitis
cystic fibrosis
pancreas divisum
abdominal trauma
17
Q

Vasculature complications from pancreatitis

A

pancreatic enzymes can erode the vessels or cause thrombosis, hemorrhage, rupture or a pseudoaneurysm.

18
Q

Bowel complications in pancreatitis

A

bowel perforation may result due to the erosion by the pancreatic enzymes.

19
Q

Pancreatic cysts occur in the following:

A
pancreatitis
cyst adenoma/adenocarcinoma
ADPKD
cystic fibrosis
congenital
cystic lymphangioma
hydatid disease
pancreaticoblastoma
20
Q

Pancreatic neoplasms:

A

extremely rare in children. may be solid or cystic.

21
Q

Pancreatic serous cytadenomas

A

benign neoplasms that arise from the acinar cells of the pancreas. ususally in head or neck of pancreas. if large may cause CBD obstruction.

numerous small cysts with proteinaceous fluid and septa are seen.

22
Q

Pancreatic mucinous cystadenomas

A

premalignant/malignant, largely occur in the body and tail of the pancreas.
Ovarian - type stroma and are more common in females.

23
Q

Pancreatic pseudocysts

A

collection of pancreatic fluid and inflammatory exudates encapsulated by fibrous tissue.

*they develop post trauma or are due to inflammatory injury to the pancreas.

most located in body and tail. may be complicated due to hemorrhage or infection.

sono: septations, internal echoes and fluid-debris levels are seen.

24
Q

Solid pancreatic neoplasm:

A

predominately endocrine.

Insulinomas- benign
Gastronomas- malignant

Adneomcarcinoma’s are the most common malignant neoplasm and similar findings as those in adults.

25
Q

Pancreaticoblastoma

A

rare solid pancreatic tumor

*associated with Beckwith Wiedemann syndrome.