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Surgical diseases of the Pancreas

Dr. Hamid Hindi

Anatomy of the Pancreas

Physiology of the Pancreas
Exocrine pancreasTrypsinChymotrypsinElastaseCarboxypeptidase ACarboxypeptidase BColipasePancreatic lipaseCholesterol ester hydrolasePancreatic α amylaseRibonucleaseDeoxyribonucleasePhospholipase AІ Endocrine Pancreas Insulin

Acute Pancreatitis

Def. Acute inflammation, usually with rapid onset of pain and tenderness, often accompanied by vomiting, and systemic inflammatory responses. Regional tissues and remote organ systems are sometimes involved. Elevated pancreatic enzymes in blood or urine usually occur, but not invariably.

Etiology of A.P.

Metabolic
Mechanical
Vascular
Infection
Alcohol Hyperlipoproteinemia Hypercalcemia Drugs Genetic Scorpion venom
Cholelithiasis Postoperative Pancreas divisum Post-traumatic E.R.P. Pancreatic duct obstruction Pancreatic duct bleeding Duodenal obstruction
Post-operative Periarteritis nodosa Atheroembolism
Mumps Coxsakie B Cytomegalovirus Cryptococcus


PATHOGENESIS

Clinical Picture

CLINICAL PICTURE
HISTORY
SYMPTOMS
SIGHNS

History

Risk factors Previous attacks?

Symptoms

Pain- upper abdominal,constant,radiates to the back(50%),Often starts after alcohol binge or heavy meal,increases in intensity rapidly. Dominant symptom in 85%-100%. Nausea Vomiting- not coupious,gastric and duodenal contents

Signs

Restlessness Rapid pulse Rapid respiratory rate Arterial hypotension Abdomen moderately distended, epigastric fullness. Grey-turner sign Cullen sign Fox sign



Special investigations
Confirm diagnosis S-amilase ( remember diff.) U-amilase S-lipase CRP ABG FBC S-Calsium

RADIOLOGY

CXR Sympathetic pleural effusion Atelectasis A.R.D.S. AXR Sentinal loop Colon cutoff sign Duodenal ileus Calcifications Obscured psoas lines 79% will have radiological signs !!!

HOW DO WE DETERMINE PROGNOSIS? ( TREATMENT)

80% Will recover without any complications 20% Will develop severe cardio-pulmonary complications or septic complications Prognostic assessment : Ranson Imrie APACHE 2 CRP Classify into mild or severe acute pancreatitis ( Atlanta clessification 1992)

TREATMENT OF ACUTE PANCREATITIS

NON-OPERATIVE To limit severity of pancreatic inflammation Inhibition of pancreatic secreation Nasogastric suction Pharmacologic Hypothermia Pancreatic irradiation Inhibition of pancreatic enzymes Corticosteroids Prostaglandins To interrupt the pathogenesis of complications Antibiotics Antacids Heparin Low molecular weight dextran Vasopressin Peritoeal lavage

TREATMENT OF ACUTE PANCREATITIS

To support the patient and treat complications Restoration and maintenance of intravascular volume Electrolite replacement Respiratory support Nutritional support Analgesia Heparin

TREATMENT OF ACUTE PANCREATITIS

Operative treatment Diagnostic laparotomy To limit the severity of the pancreatic inflammation Biliary procedures To interrupt the pathogenesis of complications Pancreatic drainage Pancreatic resection Pancreatic debridement Peritoneal lavage To support the patient and treat complications Drainage of pancreatic infection Feeding jejenostomy To prevent recurrent pancreatitis

Summary of treatment

All patients Nasogastric suction NPO Monitor and maintenance of intravascular volume Respiratory monitoring and support Antibiotics(selective) Early laparotomy only fordiagnosis Estimate prognosis by early signs Patients with severe pancreatitis Peritoneal lavage Nutritional support Suspect and treat pancreatic sepsis Heparin if hypercoagulable

Complications of acute pancreatitis

Systemic complications: Fluid imbalance Electrolite imbalance Cardiac impairmant Renal impairmant Respiratory impairmand Liver failure Local complications: Ileus Duodenal obstruction Biliary obstruction Pseudocyst formation Infected necrosis Colon necrosis

Pancreatic pseudocyst

Def. Pseudocysts are localized collections of pancreatic juice occurring as a result of pancreatic inflammation, trauma or duct obstruction.They are distinguished from other types of pancreatic cysts by their lack of an epithelial lining. Presenting symptoms: Epigastric pain Nausea Vomiting Weight loss Epigastric mass Fever Jaundice

Pancreatic pseudocyst

Investigations: Elevated s-amylase (50%) Ultrasound CT ? E.R.C.P. Natural history: Most will resolve spontaneously Treatment: Only if symptomatic Treatment options: Drainage External Internal Endoscopic surgically

CHRONIC PANCREATITIS

DEF. Chronic pancreatitis is an inflammatory disease of the pancreas characterized by destruction of its exocrine and endocrine tissue and by their replacement with fibrous scar. It is the difference in the ability to recover that is the basis for the classification of pancreatitis into acute and chronic forms.

ETIOLOGY OF CHRONIC PANCREATITIS

Alcohol Ductal obstruction Congenital or acquired strictures of the pancreatic duct Pancreas divisum Ductal obstruction due to tumors Inflammation of the ampulla of Vater Protein malnutrition Cyctic fibrosis Hypercacemic states Hereditary pancreatitis Idiopathic pancreatitis

CLINICAL MANIFESTATIONS

Abdominal pain (95%) Exocrine dysfunction (steatorrhea & creatorrhea) Endocrine dysfunction ( DM) Weight loss (75%) Few clinical findings

SPECIAL INVESTIGATIONS

Blood testsRadiology (mainstay of the diagnosis)AXRPancreatic calcifications (30-50%)CTDilated pancreatic ductCalcification of pancreasPseudocyctsE.R.C.P.“Chain of lakes” appearanceDistal bile duct stenosis

EXTRAPANCREATIC INVOLVEMENT

Common bile duct obstruction (10%) Duodenal obstruction (1%) Colonic obstruction

TREATMENT OF CHRONIC PANCREATITIS

MEDICAL Pancreatic insufficiency Diabetes mellitis Pain
SURGICAL Resections Drainage procedures

PANCREAS TUMORS

Benign v/s malignant Exocrine v/s Endocrine ( Pancreatic islet cell tumors )

ENDOCRINE TUMORS

Alpha cell Glucagon Glucagonoma Beta cell Insulin Insulinoma Delta cell Somatostatin Somatostatinoma Delta-2-cells VIP WDHA (Vipoma) G-cells Gastrin ZES (Gastrinoma)

EXOCRINE TUMORS

Adenocarcinomas Most common pancreas tumor Etiology unknown Risk factors Sigaret smoking High intake animal fat and meat Chronic pancreatitis Several hereditary disorders Hereditary pancreatitis Von Hippel-Lindau syndrome Lynch-syndrome Ataxiatelangiectasia

CLINICAL PRESENTATION

Symptoms: Early non-spesific Anorexia Weight loss Abdominal discomfort Nausea Spesific symptoms Jaundice Pruritis Moderate pain DM Unexplained attack of pancreatitis

CLINICAL PRESENTATION

Physical findings Jaundice Enlarged liver Palpable gallbladder ( Courvoisier`s law) Palpable mass ( Big pancreas tumor) Ascites Virchow-Troisier node Blumer shelf Sister Josephs node Wasting

LABORATORY DATA

LFT ( raised ALP, Bili.) CA 19-9 CA 494

RADIOLOGY

Ultrasound CT scan MRI Cholangiography E.R.C.P. P.T.C. M.R.C.P.

TREATMENT

Palliation Jaundice ( pruritis) Pain Duodenal obstruction Curritave Resection of the tumor (Whipple procedure / Pancreaticoduodenectomy )






رفعت المحاضرة من قبل: ياسر خضير احمد الجبوري
المشاهدات: لقد قام 53 عضواً و 261 زائراً بقراءة هذه المحاضرة








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