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The Curious Case of John Dick Group 3 Clinical Clerk Batch 2012 SY 2011-2012
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Objectives To discuss an intriguing case of an elderly woman with abdominal pain To elaborate on the approach to jaundice To discuss the diagnostic approaches to jaundice To present the management of obstructive jaundice and review therapeutic options
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Identifying Data L.S. 64-year-old Widow Vegetable vendor Tondo, Manila
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Chief Complaint Generalized jaundice of 1 month duration
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6 mos PTA 4 wks PTA 2 wks PTA 4 days PTA 1 wk PTAAdmission Colicky Abdominal Pain Temporal Profile Weight loss Jaundice Tea-colored urine Loss of appetite
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Past Medical History : Osteoarthritis, right ankle – took unrecalled medication for 1 month Exposure to Tuberculosis G 4 P 4 (4004) via NSD without complications No history of cancer No history of heart failure or valvular defects No history of Hepatitis B or C No hemolytic disorders No dyslipidemia No history of blood transfusion No history of needle prick injury No history of prolonged or high-dose intake of drugs (e.g. Quinacrine, Rifampicin, etc) No previous hospitalization, surgery, dental surgery
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Family History Tuberculosis – Mother No history of Cancer No history of hemolytic disorders Social History : Non-smoker, non-alcoholic beverage drinker No IV illicit drug use
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Review of Systems Weight loss (~50 kg ~36 kg in 1 month) No weakness No persistent cough, night sweats, hemoptysis, fever No edema, difficulty of breathing, orthopnea No breast lump, pain or discharge No abnormal vaginal bleeding No history of abdominal trauma, changes in bowel movement, nausea and vomiting, fatty food intolerance
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Physical Examination GeneralAwake, conscious, coherent, not in pain, appears ill-looking Vital Signs BP 90/50 mmHg HR 64 bpm Ht 154 cm RR 18 cpm T 36.4 0 C Wt 36 kg BMI 15.1 kg/m 2 HEENT Icteric sclerae, yellowish palpebral conjunctivae, yellowish oral mucosa, no tonsillopharyngeal congestion, no cervical lymphadenopathies ChestEqual chest expansion, no retractions, clear breath sounds, No spider angioma CVSAdynamic precordium, normal rate, regular rhythm, distinct S1 and S2, no murmurs, concordant apex beat and PMI at 5 th ICS LMCL
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Physical Examination Abdomen Globular, No caput medusae, No bulging flanks, Abdominal girth = 29 inches Normoactive bowel sounds, Tympanitic, Soft, Positive direct tenderness over epigastric area, No palpable masses, Liver span = 9cm, Spleen not palpable, No fluid wave, No shifting dullness, Negative Murphy’s sign
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Physical Examination ExtremitiesFull and equal pulses, no edema, no cyanosis, Generalized jaundice Mental Status Exam Oriented to person, place and time. Remote, recent past, immediate memory not impaired. Cranial NervesIntact Motor, Sensory, Cerebellar Intact
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Pertinent Findings PositiveNegative Weight lossDrug or alcohol use Abdominal enlargementBlood transfusion or donation JaundiceTattoos or IV illicit drugs Tea-colored urineHistory of Hepatitis AnorexiaFamily history of Hemolytic disordes Changes in bowel movement Nausea and vomiting Fever Fatty food intolerance History of abdominal trauma
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Pertinent Findings PositiveNegative Icteric scleraeFluid wave, shifting dullness, bulging flanks JaundiceSpider angioma, caput medusae Globular abdomen, softHepatomegaly Splenomegaly Murphy’s sign
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Assessment Primary Impression Obstructive Jaundice secondary to Pancreatic Head Mass Differential Diagnoses: TB Lymphadenitis Peribiliary cancer Choledocholithiasis
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JAUNDICECAROTENEMIA DRUG INTAKE OF PROBENECID/ RIFAMPICIN HYPERBILIRUBINEMIA EXCESSIVE PRODUCTION (Hemolytic Anemia) IMPAIRED CLEARANCE UPTAKE/CONJUGATIONEXCRETIONHEPATICPOST-HEPATIC
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Jaundice Carotenemia DRUG INTAKE PROBENECID/ RIFAMPICIN HYPERBILIRUBINEMIA Excessive intake of carotene containing food such as carrots, leafy vegetables, squash, peaches, and oranges Yellowish discoloration concentrated on palms, soles, forehead & nasolabial folds
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Jaundice Carotenemia DRUG INTAKE PROBENECID/ RIFAMPICIN HYPERBILIRUBINEMIA Excessive intake of carotene containing food such as carrots, leafy vegetables, squash, peaches, and oranges Yellowish discoloration concentrated on palms, soles, forehead & nasolabial folds
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Jaundice Carotenemia DRUG INTAKE PROBENECID/ RIFAMPICIN HYPERBILIRUBINEMIA
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Jaundice Carotenemia DRUG INTAKE PROBENECID/ RIFAMPICIN HYPERBILIRUBINEMIA
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Jaundice Carotenemia DRUG INTAKE PROBENECID/ RIFAMPICIN HYPERBILIRUBINEMIA
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Jaundice Carotenemia DRUG INTAKE PROBENECID/ RIFAMPICIN HYPERBILIRUBINEMIA (+) Jaundice (+) Tea-colored urine (+) yellow discoloration of the skin (+) Icteric sclerae (-) Murphy’s sign (-) fluid wave, bulging flanks and shifting dullness (-) spider angioma and caput medusae (-) Hepatomegaly (liver span = 9 cm) (-) splenomegaly
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HYPERBILIRUBINEMIA EXCESSIVE PRODUCTION (Hemolytic Anemia) IMPAIRED CLEARANCE Ssx of anemia (pallor, fatigue, weakness, dizziness, confusion, shortness of breath, and potential for heart failure) Usually normal colored urine and stool If inherited symptoms should have been present at an earlier age jaundice, splenomegaly, hepatomegaly, tachycardia, murmur
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HYPERBILIRUBINEMIA EXCESSIVE PRODUCTION (Hemolytic Anemia) IMPAIRED CLEARANCE
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UPTAKE/ CONJUGATION EXCRETIONHEPATICPOST-HEPATIC
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IMPAIRED CLEARANCE UPTAKE/ CONJUGATION EXCRETIONHEPATICPOST-HEPATIC Crigler-Najjar syndromes – complete/incomplete absence of UDPGT activity Gilbert’s syndrome – reduced bilirubin UDPGT activity Manifestations of disorders in conjugation should appear earlier
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IMPAIRED CLEARANCE UPTAKE/ CONJUGATION EXCRETIONHEPATICPOST-HEPATIC
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(-) spider angioma and caput medusae (-) fluid wave, bulging flanks and shifting dullness (-) Hepatomegaly (liver span = 9 cm) (-) splenomegaly
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IMPAIRED CLEARANCE UPTAKE/ CONJUGATION EXCRETIONHEPATICPOST-HEPATIC
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GallbladderBiliary TreePancreasIntestine
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Primary Impression Obstructive jaundice secondary to Pancreatic head mass r/o pancreatic ductal adenocarcinoma
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Incidence rate 37,700 cases in the US, leading to 34,300 deaths. No predilection between genders Incidence is more common within the elderly population No established early warning symptoms Overall 5-year survival rate, <5% Pancreatic Adenocarcinoma
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Causes are still unknown although it is considered that environmental causes play a role: Cigarette smoking Obesity Chronic pancreatitis History of diabetes mellitus Diet (increased intake of red meat or dairy products) Pancreatic Adenocarcinoma
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Said to arise from a series of gene mutations Early on its onset, the mass would originate within the area of the ductal epithelium and would gradually spread to adjacent areas. Pancreatic intraepithelial neoplasia invasive carcinoma Activation of the KRAS2 oncogene and inactivation of the tumour suppressor genes CDKN2A and TP53 Pancreatic Adenocarcinoma
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Presentation of the symptoms would greatly depend on the area where the tumour is located. In 80% of cases, the tumour would be located within the area of the pancreatic head and this would have a great likelihood to cause obstructive cholestasis. Abdominal pain or discomfort as well as nausea are common clinical presentations. Diagnosis and staging
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Systemic signs would include weakness, weight loss as well as anorexia. Physical examination: Signs of jaundice Wasting Hepatomegaly Ascites Routine laboratory tests might reveal anemia, abnormal liver function tests and hyperglycemia. Pancreatic Adenocarcinoma
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Common complaints would include abdominal pain with the possibility of radiating to the back. Weight loss Splenomegaly, varices in the stomach and esophagus, GI bleeding DM symptoms, glucose intolerance
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Differential Diagnoses
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TB Lymphadenitis Right hypochondriac pain, epigastric pain and tenderness, jaundice, weight loss, icterisia Philippines is endemic for Tuberculosis Involvement of abdomen (one of the common sites of extrapulmonary TB) No associated or antecedent pulmonary TB (Majority of patients do not have associated or antecedent pulmonary TB) No splenomegaly or ascites Chronic specific granulomatous inflammation of the lymph node with caseation necrosis
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Peribiliary Cancer Jaundice - presenting symptom; intermittently wax and wanes because of necrosis and sloughing or pressure opening of minimally obstructed duct Progressive weight loss, abdominal pain, loss of appetite Increased SGOT, SGPT, alkaline phosphatase Anemia Elevated Ca 19-9 Tumor arising from the distal common bile duct, duodenum and ampulla of Vater
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Choledocholithiasis Epigastric pain that come and go, cramping Jaundice, tea-colored urine and light- colored stools Increased SGPT, SGOT, alkaline phosphatase Dilated bile ducts on ultrasound The presence of stones in the common bile duct
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ConditionRuling Out Parameters Other Tests Tuberculous Lymphadenitis Low incidence 2:1 male predominance HIV infection increases likelihood Palpable liver Bilirubins Ultrasound/CT Scan ERCP CEA, Ca 19-9 Peribiliary Cancer Choledocholithiasis
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ConditionRuling Out Parameters Other Tests Tuberculous Lymphadenitis Dyspepsia and vomiting Diarrhea Pruritus Gastrointestinal bleeding Acute Pancreatitis Couvosier sign Hepatomegaly Palpable fixed epigastric mass SGPT and SGOT Alkaline phosphatase CBC Prothrombin time Bleeding and clotting times Urinalysis CA 19-9 Peribiliary Cancer Choledocholithiasis
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ConditionRuling Out Parameters Other Tests Tuberculous Lymphadenitis No signs of cholecystitis Not totally ruled out by history and PE Serum bilirubins Ultrasound CT Scan ERCP Peribiliary Cancer Choledocholithiasis
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Laboratory Work-Up
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8.16.11Reference Direct Bilirubin223.73.4-13.0 Indirect Bilirubin95.70-18 Total Bilirubin319.48.5-23.6 SGPT/ALT201.900-45 SGOT/AST220.200-35 ALP507.4830-120
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8.16.11Reference SGPT/ALT201.900-45 SGOT/AST220.200-35 ALP507.4830-120
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Tumor Markers
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CA 19-9 Patients with pancreatic carcinoma, 75-85% have elevated CA 19-9 levels. CA 19-9 value of greater than 100 U/mL is highly specific for malignancy, usually pancreatic. CEA The reference range is less than or equal to 2.5 mg/mL. Only 40-45% of patients with pancreatic carcinoma have elevated CEA levels.
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Clinical Correlation
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Sign / SymptomExplanation Epigastric pain - Likely the result of tumor compression or invasion of mesenteric, celiac, or splanchnic plexuses - Due to obstruction of hollow abdominal viscera Jaundice - Tumor compression of the common bile duct results to failure of conjugated bilirubin to be excreted, causing spillage into the systemic circulation Tea-colored Urine - Since conjugated bilirubin is soluble in water, it would be filtered by the glomerulus and would cause darkening of the urine. Light Stools - Absence or lack of bilirubin in the intestine due to impaired drainage to the duodenum Weight loss - Cancer cells compete with normal cells for nutrients. Also, tumors of the pancreas often interfere with digestion which further contributes to weight loss.
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Laboratory FindingExplanation Elevated Bilirubins - Due to impaired excretion of bilirubins, secondary to obstructed or compressed ducts Elevated SGOT, SGPT - Accumulation of hydrophobic bile acids cause increased production of free radicals leading to oxidative damage Elevated Alkaline Phosphatase - Injury to the bile ducts will cause a marked increase in the serum alkaline phosphatase since this enzyme is concentrated in the ducts Dilated intra and extrahepatic ducts - Blocking tumor at the head of the pancreas will compress on adjacent ducts and cause dilation proximal to the obstruction Dilated pancreatic ducts - As tumor grows in the back of the head of the pancreas, it causes significant obstruction to the adjacent draining ducts Anemia - Anemia of chronic disease (malignancy)
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Imaging Studies
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Ultrasound Findings Pancreatic head Intrahepatic duct dilatation Dilated pancreatic duct Extrahepatic duct dilatation
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Abdominal CT Scan August 20, 2011 BDM Imaging Center Inc.
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LIVER STOMACH AORTA LEFT KIDNEY SPLEEN INTRAHEPATIC DUCT DILATED INTRAHEPATIC DUCTS
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EXTRAHEPATIC DUCT CELIAC ARTERY CELIAC ARTERY AND SMA ARE INTACT DILATED EXTRAHEPATIC DUCT WITH NO EVIDENCE OF OBSTRUCTION
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LEFT KIDNEY RIGHT KIDNEY GALLBLADDER DUODENUM PANCREAS LIVER ATROPHIC PANCREAS & ENLARGED PANCREATIC HEAD HYDROPS OF THE GALLBLADDER
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Cholangiogram September 13, 2011 UERMMH
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Cholangiogram Plain Film Percutaneous tube in the right hemiabdomen. Tip at the right paravertebral area at the level of the L3 vertebra.
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Cholangiogram Intrahepatic ducts Gallbladder Proximal common bile duct Common hepatic duct Upon injection of contrast...
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With tube manipulation... Distal portion of the percutaneous tube Duodenum
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Therapeutics
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a.k.a. Pancreaticoduodenectomy Whipple’s procedure
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In patients with localized disease (stage I or II disease), with distal metastases excluded by prior CT scan of the abdomen and pelvis, and CT of the chest or chest x-ray, is potentially curative 5-year survival = 10%, although modern series have improved on these results.
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Chemotherapy Deoxycytidine analogue gemcitabine 1000 mg/m 2 weekly for 7 weeks followed by 1 week rest, then weekly for 3 weeks every 4 weeks thereafter
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Percutaneous transhepatic biliary drainage is used preoperatively to decompress the biliary tree and prevent complications aggravated by bile spillage. Drainage of the biliary tree by the introduction of a catheter through the liver and into the biliary tree under radiologic guidance. Also called percutaneous transhepatic cholangiodrainage. Percutaneous Biliary Drainage
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Indication for PTBD To relieve obstructive jaundice when the endoscopic retrograde approach has failed or is not indicated
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Indications for PTBD To manage infectious complications of biliary obstruction, such as cholangitis and sepsis. To decompress the biliary tree preoperatively and to assist the surgeon during surgical dissection and reconstructions.
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Indications for PTBD As initial step of other bile duct interventions, such as a biopsy of the biliary ducts or peribiliary tumors. As definitive palliation of biliary stenosis by stent placement. To provide access for transhepatic brachytherapy for cholangiocarcinoma
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Percutaneous Biliary Drainage September 2, 2011 St. Luke’s Medical Center
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Needle Dilated common bile duct
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Guide wire Cut off area
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Catheter Gallbladder
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Biopsy site
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Prognosis
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Median survival time for all patients is 4-6 months. Patients who survive for 5 years after successful surgery may still die of recurrent disease years after the 5-year survival point. The occasional patient with metastatic disease or locally advanced disease who survives beyond 2-3 years die of complications
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Thank you for your kind attention!
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Appendix
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CBC8/23 HGB94 HCT26 RBC WBC4.0 Neutrophils61.5 Lymphocytes34.9 Eosinophils3.5 Basophils0 Platelets249 8/23Ref. A/G1.81.1-2.2 Dir. Bilirubin 223.73.4-13.0 Globulin19.715-34 Indir. Bilirubin 95.70-18 Tot. bilirubin 319.48.5-23.6 Tot. protein 55.8560-83 Albumin36.1635-53 Urinalysis ColorDark Yellow TurbidityClear Reaction7.0 Sp. Gr.1.020 ProteinNegative SugarNegative RBC0-1/hpf WBC0-2/hpf Casts Bacteria Epithelial cellsfew 8/8Ref. Na131.80135-145 K4.713.6-5.5 Crea68.7745-104 8/16Reference SGPT201.900-45 SGOT220.200-35 ALP507.4830-120
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Gallbladder Pathology No radiation to right shoulder, no fatty food intolerance, no vomiting, no post-prandial pain, (-) Murphy’s sign Biliary Tree Pathology No fatty food intolerance; Not entirely ruled out Pancreatic Pathology Non-alcoholic Jaundice
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