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
|