• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/74

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

74 Cards in this Set

  • Front
  • Back
Whipple's Triad
1) Symptomatic HYPOglycemia during fasting
2) Serum glucose less than 50mg/dl
3) Relief of symptoms with glucose administration
**Associated with insulinomas
Presentation of Glucagonoma
1) Severe dermatitis - Necrolytic Migratory Erythema
2) Mild diabetes

**Pts often first treated by dermatologist
Failure of normal clockwise rotation of the ventral pouch results in...
Annular pancreas → Double bubble sign, bilious vomiting
The main pancreatic duct
Duct of Wirsung
Pancreatic Divisum
Occurs when the ducts do not fuse → unfused proximal dorsal is accessory duct of Sanrorini
Contents of pancreatic acincar cells
Digestive enzymes (i.e., amylase, lipase, phospholipase A2, trypsin, elastase)
Function of pancreatic ductal cells
Secrete electrolyte solution high in bicarbonate
Products of pancreatic endocrine cells
Alpha cells – glucagon
Beta cells – insulin
Delta cells – somatostatin
F cells – pancreatic polypeptide
Islets – VIP, serotonin, etc
2 MCC of acute pancreatitis
1) Alcohol abuse
2) Gallstones
*Others: ERCP, trauma, HLD, hypercalcemia, Ascaris lumbricoides, medications)
Medications known to cause pancreatitis
1) Azathioprine
2) Furosemide
3) Glucocorticoids
4) Cimetidine
Signs & Symptoms of acute pancreatitis
1) Abdominal pain
2) Nausea / Vomiting
3) Anorexia
Signs of hemorrhagic pancreatitis
1) Grey Turner sign – retroperitoneal hemorrhage of the flank
2) Cullen sign – hemorrhage around the umbilicus
3) Fox sign – hemorrhage around the inguinal ligament
Ranson’s Criteria
Prognostic indicator in pancreatitis
Patients with more than 3 Ranson’s criteria are at high risk of complicated pancreatitis
Mortality sharply rises with more than 3 Ranson’s criteria
Parameters of Ranson’s criteria
1) Age
2) WBCs
3) LDH
4) Aspartate aminotransferase (AST)
5) Glucose

*Clinical prediction rule for predicting the severity of acute pancreatitis
Treatment of acute pancreatitis
*Nonoperative, unless complications develop (i.e., necrosis or infection)
1) Aggressive fluid resuscitation
2) Intubation and mechanical ventilation → if pulmonary dysfunction occurs
3) Nasogastric decompression
4) Nutritional support (usually TPN)
5) ERCP with endoscopic sphincterectomy → if gallstone pancreatitis or biliary obstruction
6) Prophylactic antibiotics (i.e., imipenem – cilastin)
Gallstone pancreatitis
Pancreatitis in the setting of cholelithiasis
Intraoperative cholangiography (IOC)
Done during laproscopic cholecystectomy to confirm the absence of common bile duct obstruction
Pancreatic abscesses
Well-cirumscribed, polymicrobial abscesses
Should be drained percutaneously (operatively if attempts fail or there is necrosis)
Why are patients with sterile necrotizing pancreatitis treated nonoperatively for several weeks?
To better delineate viable and nonviable pancreatic tissue
*Imipenem-cilastatin decreases the infection rate in these patients
Treatment of infected necrotizing pancreatitis
Necrosectomy (debridement of necrotic tissue) and operative drainage
IV antibiotics once organism sensitivity is known
Chronic pancreatitis
Irreversible parenchymal fibrosis
Presentation of chronic pancreatitis
1) Recurrent acute pancreatitis
2) Chronic abdominal pain
3) Anorexia and weight loss
4) Malabsorption and steatorrhea
5) DIABETES
MCC of chronic pancreatitis in US
Alcohol abuse
CT findings of chronic pancreatitis
1) Atrophied gland
2) Dilated pancreatic duct
3) CALCIFICATIONS
Relative indications for surgery of chronic pancreatitis
1) Refractory, disabling pain
2) Concomitant malignancy
3) Biliary obstruction
4) Complications of pseudocysts
Operative techniques for chronic pancreatitis
1) Drainage procedures – Duval, Peustow, Frey
2) Resection procedures – Distal pancreatectomy, Whipple procedure, Total pancreatectomy
3) Splanchnicectomy – celiac ganglion ablation for pain control
Pancreatic Pseudocyst
Non-epithelialized, encapsulated pancreatic fluid collection
*Usually seen several weeks after bouts of acute pancreatitis
Symptoms of pseudocysts
1) Pain
2) Fever
3) Weight loss
4) Bowel obstruction
Diagnosis of pseudocyst
CT scan
Size of pseudocysts that resolve spontaneously
<5 cm
Size of pseudocyst that requires drainage
>6 cm
Symptoms of pancreatic insufficiency
Malabsorption and steatorrhea
Diagnosis of pancreatic insufficiency
1) Fecal fat testing
2) Secretin or CCK test
Treatment of pancreatic insufficiency
HIGH CARB, HIGH PROTEIN diet with pancreatic enzyme replacement
% of pancreatic carcinoma of ductal cell origin
90%
% of pancreatic adenocarcinomas arising in the head of the pancreas
67%
Sites of metastasis of pancreatic adenocarcinomas
1) Lymph nodes
2) Liver
3) Peritoneal surfaces
Five-year survival rates of pancreatic cancer in US
0 – 10%
Mucinous Cystadenoma
Often contains malignant cells
60% 5-year survival after surgery
Tumor-Node-Metastasis (TNM) Staging of Pancreatic Cancer
Stage 1 – Limited or no extension beyond pancreas
Stage 2 – Extension incompatible with resection
Stage 3 – Regional nodal disease
Stage 4 – Distant metastasis
Presentation of pancreatic cancer
1) Weight loss
2) Jaundice
3) Abdominal pain
4) Nausea and anorexia
5) Hepatomegaly
6) Vomiting due to duodenal obstruction
*ELEVATED DIRECT BILIRUBIN, alk phos, and amylase
Contraindications to curative resection of pancreatic cancer
1) Liver metastasis
2) Peritoneal metastases
3) Nodal metastases beyond zone of resection (e.g., periaortic)
4) Tumor invasion of SMA
Pre- or postoperative adjuvant chemoradiotherapy for pancreatic cancer
5-fluorouracil and external beam radiation
Complications of pancreaticoduodenectomy
1) Delayed gastric emptying
2) Pancreatic fistula (10 – 20%)
3) Infection
4) Bile leak
5) Pancreatitis
MC endocrine tumor of the pancreas
Insulinoma
*90% are benign
Symptoms of insulinoma
1) Catecholamine surge-related symptoms: Palpitations, diaphoresis, tachycardia
2) Whipple’s Triad
Whipple’s Triad
1) Symptomatic HYPOglycemia during fasting
2) Serum glucose less than 50mg/dl
3) Relief of symptoms with glucose administration
**Associated with insulinomas
Diagnosis of insulinoma
Concomitant measurement of insulin and glucose levels during fasting period of 12-18 hours
*Measuring proinsulin or C-peptide excludes surreptitious insulin
Presentation of Gastrinomas
1) Abdominal pain
2) Intractable peptic ulcer disease (PUD)
Chromosomal abnormality associated with Gastrinomas
HER-2/neu proto-onogene amplification
Diagnosis of gastrinoma
Secretin test
% of gastrinomas that are malignant
50%
Presentation of Vasoactive Intestinal Peptide Tumors (VIPomas)
WDHA syndrome – Watery Diarrhea, Hypokalemia, Achlorhydria
*Aka Verner-Morrison syndrome
% of VIPomas with metastatic disease to LNs of liver
50%
Presentation of Glucagonomas
1) Severe dermatitis → Necrolytic Migratory Erythema
2) Diabetes
3) Stomatitis
4) Weight loss
Necrolytic Migratory Erythema
Red, blistering rash that spreads across the skin, particularly the lower abdomen, buttocks, perineum, and groin
Treatment of all pancreatic endocrine tumors
Resection, unless there’s metastatic disease
Resection of insulinomas
Enucleation
Resection of VIPomas and glucagonomas
Distal pancreatectomy (tail of pancreas)
*Octreotide may help ameliorate symptoms
Incurable pancreatic endocrine tumor
Somatostatinoma
MC location of accessory spleens
Splenic hilum
Primary indication for splenectomy
Splenic trauma
Indications for surgical intervention after splenic trauma
1) Hemodynamic instability
2) Arterial “blushing” or pooling of contrast on abdominal CT
3) >2 units PRBC
Autosomal dominant disease treated with splenectomy
Hereditary Spherocytosis (HS)
*RBC membranes are deformed; RBCs sequestered and destroyed by spleen
At which age should splenectomy be performed for Hereditary spherocytosis?
After age 4
Clinical manifestations of ITP
Thrombocytopenia → Purpura, Ecchymoses, Bleeding from mucosal surfaces, Hematuria
Treatment of ITP
1) Corticosteroids and IV gamma globulin
2) Vinca alkaloids, cyclophosphamide, danazol, plasmapheresis
3) Splenectomy
4) Platelet transfusions POST-OP
Pentad of TTP
1) Fever
2) Purpura
3) Hemolytic anemia
4) Hematuria
5) Neurologic changes
Treatment of TTP
1) Plasmapheresis
2) Splenectomy (refractory disease)
MCC of splenic abscess
Hematogenous spread of bacterial infection (endocarditis and IV drug abuse)
Hypersplenism
Splenomegaly, decreased dysfunctional circulating platelets, & responsive BM hypertrophy
Mortality of Overwhelming Postsplenectomy Infection (OPSI)
80 – 90%
Causes of OPSI
Encapsulated organisms (Pneumococcus, Meningococcus, Haemophilus influenza B)
When should vaccinations be given before splenectomy?
10 days before surgery