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Published byFelicity May Modified over 8 years ago
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In 15% of patients, cholecystectomy fails to relieve the symptoms for which the operation was performed. ‘post-cholecystectomy’ syndrome. problems are usually related to the preoperative symptoms and are continuation of those symptoms. Full investigation should be undertaken to confirm the diagnosis presence of a stone in the common bile duct, a stone in the cystic duct stump or operative damage to the biliary tree.
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best DIAGNOSED by MRCP or ERCP. The latter has the added advantage that, if a stone is found in the common bile duct, it can be removed.
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Patients with symptoms developing either immediately or delayed after a cholecystectomy, particularly jaundice,need urgent investigation.
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immediate ultrasound scan. whether there is intra- or extrahepatic ductal dilatation. The anatomy defined by MRCP. ERCP therapeutic manoeuvres : removal of an obstructing stone insertion of a stent across a biliary leak. If a fluid collection is present in the subhepatic space, drainage catheters may be required. These can be inserted under radiological control or, if this expertise is not available, at open operation.
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Small biliary leaks will usually resolve spontaneously, especially if there is no distal obstruction. Should the common bile duct be damaged, the patient should be referred to an appropriate expert for reconstruction of the duct.
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About 15% of injuries recognised at the time of operation. In 85% of cases, the injury declares itself postoperatively by: (1) a profuse and persistent leakage of bile if drainage has been provided, or bile peritonitis if such drainage has not been provided; (2) deepening obstructive jaundice.
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When the obstruction is incomplete, jaundice is delayed until subsequent fibrosis renders the lumen of the duct inadequate. The surgical repair and subsequent outcome is related to the level of injury, which is determined using the Bismuth classification
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Bismuth classification Type I Low common bile duct; stump > 2 cm Type II Middle common hepatic duct; stump < 2 cm Type III Hilar – confluence of right and left ducts intact Type IV Right and left ducts separated Type V Involvement of the intrahepatic ducts
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In the debilitated patient, temporary external biliary drainage by passing a catheter percutaneously into an intrahepatic duct. stents may be passed through strictures at the time of ERCP and left to drain into the duodenum. When the general condition improved, Definitive surgery can be undertaken. The principles of surgical repair are maintenance of duct length and restoration of biliary drainage.
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For benign stricture or duct transection, the preferred treatment is immediate Roux-en-Y choledochojejunostomy by an experienced surgeon. For a stricture of recent onset through which a guidewire can be passed, balloon dilatation with insertion of a stent. The outcome of such surgery is good, with 90% of patients having no further cholangitis or stricture formation.
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PRIMARY STONES:occure years after a cholecystectomy or development of new pathology, such as infection of the biliary tree or infestation by Ascaris lumbricoides or Clonorchis sinensis. Secondary stone (missed stone )from gall bladder Any obstruction to the flow of bile can give rise to stasis with the formation of stones within the duct. The consequence of duct stones is either obstruction to bile flow or infection.
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Stones in the bile ducts are more often associated with infected bile (80%) than are stones in the gall bladder
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Symptoms The patient may be asymptomatic May has bouts of pain, jaundice and fever. The patient is often ill and feels unwell. The term ‘cholangitis’ is given to the triad of pain, jaundice and fevers, sometimes known as ‘Charcot’s triad’. Signs Tenderness may be elicited in the epigastrium and the right hypochondrium. In the jaundiced patient, it is useful to remember Courvoisier’s law – in obstruction of the common bile duct due to a stone, distension of the gall bladder seldom occurs; the organ is usually already shrivelled. In obstruction from other causes, distension of the gall bladder is common by comparison.
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Management Full supportive measures are required with rehydration, correction of clotting abnormalities and treatment with appropriate broad-spectrum antibiotics.
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Once the patient has been resuscitated, relief of the obstruction is essential. Endoscopic papillotomy is the preferred first technique with a sphincterotomy, removal of the stones using a Dormia basket or the placement of a stent if stone removal is not possible. If this technique fails, percutaneous transhepatic cholangiography can be performed to provide drainage and subsequent percutaneous choledochoscopy. Surgery, in the form of choledochotomy, is now rarely used for this situation, as most patients can be managed by minimally invasive techniques
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The aim of this surgery is to drain the common bile duct and remove the stones by a longitudinal incision in the duct. When the duct is clear of stones, a T-tube is inserted and the duct closed around it; the long limb of the T-tube is brought out on the right side, and the bile is allowed to drain externally. When the bile has become clear and the patient has recovered, a cholangiogram is performed, usually 7– 10 days following operation. If residual stones are found, the T-tube is left in place for 6 weeks so that the track is ‘mature’. The retained stones can be removed percutaneously by an interventional radiologist (Burhenne technique)
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Causes of benign biliary stricture Congenital ■ Biliary atresia Bile duct injury at surgery ■ Cholecystectomy ■ Choledochotomy ■ Gastrectomy ■ Hepatic resection ■ Transplantation Inflammatory ■ Stones ■ Cholangitis ■ Parasitic ■ Pancreatitis ■ Sclerosing cholangitis ■ Radiotherapy Trauma Idiopathic
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■ Ultrasonography ■ Cholangiography via T-tube, if present ■ ERCP ■ MRCP ■ PTC ■ Multidetector row CT
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Benign tumours of the bile duct uncommon less than 0.1% of biliary tract operations. clinical presentation may mimic the more common conditions such as cholecystitis, choledocholithiasis,cancer of the bile duct and pancreatic cancer.
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Benign neoplasms classificationas follows: papilloma and adenoma; multiple biliary papillomatosis; granular cell myoblastoma; neural tumours; leiomyoma; endocrine tumours.
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Carcinoma may arise at any point in the biliary tree, from the common bile duct to the small intrahepatic ducts
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Incidence rare malignancy accounting for 1–2% of new cancers in a western practice. two-thirds of patients being older than 65 years. the tumour is usually an adenocarcinoma (cholangiocarcinoma), predominantly in the extrahepatic biliary system.
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Patients with a history of followings are at increased risk of developing the disease. ulcerative colitis, hepatolithiasis, Choledochal cyst or sclerosing cholangitis
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longstanding history of sclerosing cholangitis increases the risk of developing biliary tract cancer by 20-fold compared with the normal population.
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liver fluke infestations in the Far East are also associated with cholangiocarcinoma. Opisthorchis viverrini infestation is important in Thailand, Laos and western Malaysia. These parasites induce DNA changes and mutations through production of carcinogens and free radicals, which stimulate cellular proliferation in the intrahepatic bile ducts and can ultimately lead to invasive cancer.
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slow-growing tumours that invade locally and metastasise to local lymph nodes. Distant metastases to the peritoneal cavity, liver and lung may occur. Jaundice is the most common presenting feature. Abdominal pain, early satiety and weight loss are also commonly seen.
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On examination, Jaundice is evident, cachexia often noticeable a palpable gall bladder is present if the obstruction is in the distal common bileduct (Courvoisier’s sign).
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Investigations Biochemical investigations will confirm the presence of obstructive jaundice (elevated bilirubin, alkaline phosphatase and gamma- glutamyl transferase). The tumour marker CA19-9 may also be elevated. Non-invasive studies such as ultrasound and CT scanning define the level of biliary obstruction, the locoregional extent of disease and the presence of metastase
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For proximal tumours, percutaneous transhepatic cholangiography is the most useful modality. PTC outlines the anatomy of the tumour and the intrahepatic biliary system. it allows percutaneous biliary drainage, samples can be obtained for cytology to confirm the diagnosis.
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. For distal tumours, an ERCP is preferred as an endobiliary stent can be placed across the obstructing lesion. Again, cytology or biopsies can be taken for diagnosis.
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Treatment depends on the site and extent of disease. ONLY 10–15% are suitable for surgical resection. . Most patients are inoperable,
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Depending on the site of disease, resection may involve partial hepatectomy and reconstruction of the biliary tree. Distal common duct tumours may require a pancreaticoduodenectomy. The perioperative mortality rate is now less than 5%. The median survival is 18 months, with 20% of patients surviving 5 years post resection.
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Survival appears to be better for distal tumours compared with those involving the upper third of the biliary tree. Adjuvant chemotherapy or radiotherapy has a limited role and is not considered standard therapy.
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Bile duct cancer ■ Rare, but incidence increasing ■ Presents with jaundice and weight loss ■ Diagnosis by ultrasound and CT scanning ■ Jaundice relieved by stenting ■ Surgical excision possible in 5% ■ Prognosis poor – 90% mortality in 1 year
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Incidence This is a rare disease variable by geographical region and racial/ethnic groups. The highest incidence is in Chileans, American Indians and in parts of northern India, where it accounts for as much as 9.1% of all biliary tract disease.
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. In western practice, gall bladder cancer accounts for less than 1% of new cancer diagnoses. The patients are usually older, in their sixties or seventies.
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The aetiology is unclear, association with preexisting gallstone disease. Calcification of the gall bladder is associated with cancer in 10–25% cases. Infection may promote the development of cancer as the risk of carcinoma in typhoid carriers is significantly increased.
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Pathology The majority of cases are adenocarcinoma (90%). ; the tumour is most commonly nodular and infiltrative, with thickening of the gall bladder wall, often extending to the whole gall bladder.
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The tumour spreads by direct extension into the liver, seeding of the peritoneal cavity and involvement of the perihilar lymphatics and neural plexuses. At the time of presentation, the majority of tumours are advanced.
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Clinical features Patients may be asymptomatic at the time of diagnosis. . If symptoms are present, they are usually indistinguishable from benign gall bladder disease such as biliary colic or cholecystitis, particularly in the older patient. Jaundice and anorexia are late feature. A palpable mass is a late sign
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Investigation Laboratory findings may be consistent with biliary obstruction or non-specific findings such as anaemia, leucocytosis, mild elevation in transaminases and increased erythrocyte sedimentation rate (ESR) or C-reactive protein (CRP).
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The level of serum CA19-9 is elevated in 80% of patients. The diagnosis is made on ultrasonography defined by a multidetector row CT scan, percutaneous biopsy confirming the histological diagnosis. laparoscopy is useful in staging the disease, as it can detect peritoneal or liver metastases that would preclude further surgical resection.
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Treatment and prognosis Occasionally, the diagnosis is made by histological examination of a gall bladder removed for ‘benign’ gallstone disease. For early stage disease confined to the mucosa or muscle of the gall bladder, no further treatment is indicated. However, for transmural disease, a radical en bloc resection of the gall bladder fossa and surrounding liver along with the regional lymph nodes should be performed.
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The disease has a very poor prognosis with the median survival less than 6 months and a 5-year survival of 5%. The value of adjuvant therapy is unproven.
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Gall bladder cancer ■ Rare ■ Presents as for benign biliary disease (gallstones) ■ Diagnosis by ultrasound and CT scanning ■ Excision in less than 10% – remainder palliative treatment ■ Prognosis poor – 95% mortality in 1 year
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1) Correct Anaemia if Present 2) Good Hydration with i.v. fluids to prevent dehydration & maintain the Renal Function 3) Mannitol i.v. infusion to maintain osmotic diuresis and prevent Bilirubin from precipitating in the tubules. 4) Vitamine K injectable to activate important clotting factors (fat soluble vitamines are not absorbed) 5) Add 5% Glucose Water to help build up Liver glycogen 6) Antibiotics Broad Spectrum
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blunt or penetrating abdominal trauma. Operative trauma is perhaps more frequent than external trauma. physical signs are those of an acute abdomen. Management depends on the location and extent of the biliary and associated injury. In the stable patient, a transected bile duct is best repaired by a Roux-en-Y choledochojejunostomy. Injuries to the gall bladder can be dealt with by cholecystectomy.
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