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PANCREAS

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Psedocyst of the Pancreas A. Causes 1 ... adenoma of the pituitary, parathyroid, ... – PowerPoint PPT presentation

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Title: PANCREAS


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  • I. Pancreas
  • A. Anatomy
  • - retroperitoneal
  • - extends transversely behind the stomach
  • - weight approximately 85 grams
  • - length 12-15 cm.

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  • 1. Anatomic relationships
  • a. head of the pancreas lies over the
    aorta and under the stomach and transverse
    colon, posteromedial to the IVC
  • i. superior limit portal vein
  • ii. anterior limit gastro-duodenal
    artery
  • iii. CBD courses posteriorly to the head
    and partially within
  • iv. Common blood supply with the duodenum

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  • b. uncinate process lies posterior
    to the SMV and anterior to the IVC
  • c. tail closely related to the spleen
  • d. neck lies at the confluence of splenic
    and mesenteric veins

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  • B. Blood supply
  • 1. Anterior and posterior arcades supply the
    head of the pancreas superior component comes
    from the gastroduodenal artery and the inferior
    component comes from the superior mesenteric
    artery
  • 2. Inferior pancreatic artery runs inferior
    to the organ, in intimate contact with the
    pancreas

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  • 3. Superior pancreatic artery present in
    50-90 of patients
  • a. arises from the splenic artery, hepatic
    artery, superior mesenteric or iliac artery
  • b. postero-superior portion of the neck and
    body of the pancreas
  • 4. Splenic and left gastroepiploic artery
    supplies body and tail of the pancreas

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  • 5. Venous drainage
  • a. follows the course of the arteries
  • b. confluence of right gastroepiploic
    vein, anterosuperior pancreaticoduodenal vein,
    middle colic vein
  • c. forms the gastrocolic trunk which empties
    directly to the SMV at the inferior border of
    the neck of the pancreas

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  • 6. Ductal system drains into the duodenum
  • a. Duct of Wirsung empties into the
    ampulla of Vater together with the
    CBD
  • b. Duct of Santorini drains into the minor
    papilla approximately 2 cm above and medial
    to the ampulla of Vater (minor ductal system)

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  • II. Pancreatitis
  • A. Acute pancreatitis
  • 1. Gallstone pancreatitis
  • a. needs a common channel between the CBD
    and the pancreatic duct
  • b. high proportion of causes with gallstone
    pancreatitis have recoverable biliary calculi
    in the stools
  • c. spasm of the sphincter of Odi as a stone
    passes causes reflux of bile into the
    pancreatic duct which results in the
    destruction of the pancreatic parenchyma

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  • 2. Alcohol pancreatitis
  • a. alcohol causes increase in protein
    concentration in the pancreatic juice ?
    calcifications in the duct
  • b. ductal obstruction causes inflammation
    ? destruction of parenchyma

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  • 3. Post-operative pancreatitis
  • a. occurs ususally after gastric, biliary
    tract surgery, or splenectomy
  • b. ligation or laceration of the duct may
    be the cause of the pancreatitis
  • c. mortality approximately 50

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  • B. Clinical manifestations of acute pancreatitis
  • 1. mild abdominal discomfort to profound
    shock
  • 2. epigastric pain radiating to the back with
    nausea and vomiting
  • 3. discomfort may be relieved by sitting and
    aggravated by lying down

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  • 4. may have mild to moderate abdominal
    tenderness
  • 5. may present with a surgical abdomen
  • 6. severe pancreatitis may lead to
    retroperitoneal hemorrhage which leads to
  • a. 3rd space fluid loss
  • b. hypovolemia
  • c. hypotension
  • d. tachycardia e. blood dissection Grey
    Turners sign (flank ecchymosis)
  • - Cullens sign (periumbilical ecchymosis

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  • 7. pain usually follows 1-4 hours after a
    heavy meal and intake of alcohol
  • C. Diagnosis
  • 1. History and Physical Exam
  • a. serum amylase increased in 95 of
    cases 5 false negative
  • i. 75 of patients with abdominal pain
    and increased amylase have pancreatitis

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  • ii. other causes of increased amylase
  • - acute cholecystitis
  • - CBD stone with or without cholangitis
  • - Perforated peptic ulcer
  • - Strangulated small bowel
  • - acute alcoholism
  • - Cancer of the pancreas
  • - Mumps

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  • iii. amylase level over 1,000
    Somogyi-Nelson units often indicates
    biliary tract disease with panceatitis
  • iv. 200-500 units indicates alcoholic
    pancreatitis

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  • b. amylase creatinine ratio
  • - diagnostic when amylase output in the
    urine exceeds 300 u in one hour and ratio of
    amylasecreatinine clearance of gt5
  • c. serum calcium - lt7.5 mg/dl generally
    indicates poor prognosis
  • d. radiology (x-ray) relatively insensitive
  • e. barium studies
  • i. widened duodenal C-loop
  • ii. Pad sign obliteration of the
    duodenal mucosal folds

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  • f. ultrasound swelling of the pancreas
    and loss of tissue planes
  • g. CT scan findings similar to ultrasound
    but with a higher resolution

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  • D. Treatment
  • 1. Resuscitation replacement of fluid losses
    and electrolytes
  • 2. Blood transfusion in hemorrhagic
    pancreatitis
  • 3. Calcium gluconate through IV
  • 4. NGT suction decrease GIT distension and
    pancreatic stimulation

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  • 5. Antibiotics reduce risk of abscess
    formation
  • 6. Meperidine
  • 7. Surgery
  • a. confirm diagnosis in cases which do not
    respond medically
  • b. relieve ductal obstruction
  • c. drain the lesser sac

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  • E. Prognosis Ransons Criteria
  • 1. Admission
  • a. gt 55 years old
  • b. WBC count gt 16000
  • c. FBS gt 200 mg/dl
  • d. LDH gt 350 units/ml
  • e. SGOT gt 250

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  • 2. 48 hours after admission
  • a. drop in hematocrit by gt 10
  • b. increase in BUN of 5 mg/dl
  • c. calcium level lt 8 mg/dl
  • d. PaO2 below 60 mmHg
  • e. base deficit gt 4 meq/L
  • f. third space fluid loss gt 6 L

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  • Prognosis
  • Number of criteria present Mortality rate
  • 0-2 0.9
  • 3-6 33
  • 7-8 100

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  • III. Chronic Pancreatitis
  • - clinical entity rather than a pathologic
    process
  • - organ becomes small, indurated and nodular and
    edges become rounded
  • - alternating areas of strictures and
    dilatations in the duct with calcifications
  • -primary etiology chronic alcoholic
    pancreatitis with progressive fibrosis without
    ductal dilatation or calcification

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  • A. Clinical manifestation
  • 1. late 30s or 40s
  • 2. history of alcoholism and recurrent
    attacks of pancreatitis
  • 3. pain
  • 4. may diabetes or steatorrhea
  • 5. frequent finding of pseudocyst
  • 6. anorexia and weight loss

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  • B. Diagnosis
  • 1. upper GI series
  • 2. ERCP
  • 3. ultrasound/CT scan
  • 4. calcifications on x-rays

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Calcifications of Chronic Pancreatitis
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Calcifications of Chronic Pancreatitis
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  • C. Treatment
  • 1. analgesics
  • 2. endocrine and exocrine replacement
  • 3. stop alcohol intake
  • 4. surgery (Peustow procedure)

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  • IV. Psedocyst of the Pancreas
  • A. Causes
  • 1. pancreatitis 75
  • - alcoholic pancreatitis
  • - 4th and 5th decade of life
  • 2. trauma 25

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  • B. Pathology
  • 1. fibrous wall surrounding a collection of
    pancreatic juice and necrotic or suppurative
    pancreatic juice
  • 2. unilocular and located in the lesser sac
  • 3. fluid varies from clear and colorless to
    brown or green

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  • C. Clinical manifestations
  • 1. pain, fever, and ileus appearing 2-3
    weeks after an initial attack of pancreatitis
  • 2. pain radiating to the back
  • 3. jaundice
  • d. non-tender palpable mass (75 of
    patients)
  • 4. change in size of the mass due to partial
    drainage

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  • D. Diagnosis
  • 1. continued elevation of serum amylase
  • 2. CT scan diagnostic tool of choice
  • 3. ultrasound
  • 4. upper GI series
  • 5. ERCP

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  • E. Treatment
  • 1. surgery
  • a. to prevent complications such as
    infection, hemorrhage, rupture
  • b. pseudocysts rarely resolve once thick
    fibrous wall has developed
  • c. pseudocyst should be treated only after
    5-6 weeks from discovery

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  • 2. types of surgery
  • a. external drainage
  • b. internal drainage - best
  • i. cystenterostomy
  • ii. cystgastrostomy
  • c. cyst wall should be excised for
    histopathology to rule out malignancy

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  • V. Pancreatic Tumors
  • A. Etiology
  • 1. cigarette smoking
  • 2. coffee
  • 3. biliary lithiasis

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  • B. Pathology
  • 1. Cystadenoma/Cystadenocarcinoma
  • a. rare predilection for females
  • b. cystic spaces divided by firbous septa
    vascular
  • c. better prognosis than adenocarcinoma
  • d. Tx. - resection

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  • 2. Adenocarcinoma
  • a. 90 of cases usually at the head
  • b. periampullary malignancy
  • i. head of the pancreas 83
  • ii. Ampulla of Vater 10
  • iii. Duodenum 4
  • iv. Common bile duct 3

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  • c. Clinical manifestations
  • i. weight loss most common
  • ii. pain dull epigastric pain that
    radiates to the back aggravated by eating
  • iii. progressive jaundice 75 head of
    the pancreas

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  • iv. anorexia and weakness 50
  • v. pruritus
  • vi. hepatomegally
  • vii. enlarged palpable gallbladder
    Courvesiures gallbladder

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  • d. Laboratory work-up
  • i. alkaline PO4, transaminases, Bilirubin
  • ii. UGIS
  • iii. CT scan CT scan guided biopsy
  • iv. ERCP/PTC

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  • e. Treatment
  • i. Prior to surgery improve overall
    condition of the patient
  • ii. Whipples surgery for resectable
    lesions renal failure most common
    complication
  • iii. Cholecystojejunostomy/ Gastro-
    jejunostomy bypass for unresectable
    lesions
  • iv. injection of 95 alcohol to the celiac
    plexus relief of pain

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  • v. poor risk patients
  • - PTC/PTBD
  • - 5-FU/external beam radiation

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  • 3. Zollinger-Ellison Sybdrome Ulcerinogenic
    Tumors of the Islets
  • a. malegtfemale 3rd to 4th decade
  • b. slow growing tumor of the Islets of
    Langerhan
  • c. associated with Multiple Endocrine
    Neoplasia adenoma of the pituitary,
    parathyroid, pancreatic islets (beta
    cells), and adrenal cortex
  • d. secretes GASTRIN

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  • e. Triad
  • i. fulminant and complicated peptic ulcers
    often in atypical locations
  • ii. Extreme gastric hypersecretion
  • iii. Non- beta cell tumor of the Islets

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  • f. signs and symptoms
  • i. acid peptic disease
  • ii. Distressing watery diarrhea
  • iii. steatorrhea

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  • g. diagnosis
  • i. UGIS
  • ii. Gastroscopy
  • iii. Serum gastrin determination
  • iv. CT scan

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  • h. treatment
  • i. total gastrectomy
  • ii. Resection of the tumor
  • iii. Proton pump inhibitor
  • iv. Streprozotocin - metastasis

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  • 4. Hyperinsulinism Islet cell tumor
  • - b-cells hypersecretion of insulin causing
    hypoglycemia
  • a. pathology
  • i. benign adenoma 75
  • ii. Suspected malignant 13
  • iii. Clearly malignant 12
  • iv. Diffuse adenomatosis
  • v. size of the tumor has no relation to
    severity

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  • b. clinical manifestation
  • i. 4th-7th decade
  • ii. Associated with MEA-I hyperinsulinism
  • iii. Two general forms
  • - rapid fall of blood sugar
  • - gradual fall in blood sugar

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  • iv. Whipple Triad
  • - hypoglycemic attack during fasting or
    exertion
  • - FBS gt 50 mg/dl
  • - symptoms relieved by intake of glucose

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  • c. diagnosis
  • i. blood sugar and insulin levels
  • ii. Pancreatic angiography and venous
    sampling
  • iii. CT scan

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  • d. treament
  • i. pre-operative management
  • - adequate provision of glucose
  • - ACTH and Cortisol
  • - Diazoxide inhibits release of insulin

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  • ii. Surgery
  • - benign excision
  • - malignant pancreatic resection
  • - improvement seen 30 minutes after
    excision of the lesion
  • - Streptozoticin - metastasis
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