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DIAGNOSTIC EVALUATION & STAGING
GALL BLADDER
CARCINOMA
SAMBHAVI JOSHI, 79, 2K17
Dr. ZAHID IQBAL MIR (SENIOR RESIDENT)
MBBS, MS Surgery, DNB Surgery
DIAGNOSTIC EVALUATION
PATIENTS WITH SYMPTOMATIC CHOLELITHIASIS
Screening – Ultrasound
Additional cross-sectional imaging [CT, MRI/MRCP] in
patients who have concerning findings on US
• Calcification
• a mass protruding into the lumen
• loss of interface between gallbladder and liver
• direct liver infiltration
• gallbladder polyps ≥10 mm
• thickened gallbladder wall not explained by
cholecystitis
USG
vInitial diagnostic study for presumed gallbladder
disease
vOverall accuracy of USG for staging of GBC is
limited
USG FINDINGS - MALIGNANCY
üMural thickening
ücalcification
ümass protruding into lumen
üfixed mass in GB
üloss of interface between gb and liver
üdirect liver infiltration
ØPolyp over 1 cm in diameter - invasive
§ FNAC (cholesterolosis/GBC)
§ Adenoma/GBC – less accurate
§ CT/MRI required
ØPolyp less than 1 cm
§ adenoma/ papilloma/ cholesterosis/ GBC less likely
COLOR DOPPLER - VASCULARITY
• pulsatile flow - seen in most cases
• continuous flow pattern
• Doppler sensitivity is mandatory for diagnosis of GBC in stage T 1 a
Ultrasound image showing intraluminal
polypoid gallbladder wall mass (arrow) but
without extraluminal extension.
Ultrasound image of gallbladder mass
with loss of continuity of gallbladder wall
(arrow), suggesting extraluminal growth.
Asymmetric gallbladder wall thickening (arrow) in a patient with GBC
SUSPICIOUS ULTRASOUND FINDINGS OR INCIDENTAL
GALLBLADDER CANCER AT CHOLECYSTECTOMY
üPatients who have concerning findings on US -
Evaluation of potential resectability is the key factor
üIncidentally diagnosed GBC following simple
cholecystectomy -Apropriate imaging (and
detailed histopathologic analysis) is needed to
decide whether further resection is necessary
CECT
• CT is more useful than US for detecting lymph node
involvement, adjacent organ invasion, and distant
metastasis.
INDICATIONS
• USG detected gallbladder lesion that may
represent GBC
• Incidentally diagnosed GBC following simple
cholecystectomy.
CT FINDINGS - GBC
üPolypoid mass protruding into the lumen/ filling it
üFocal or diffuse thickening of gallbladder wall.
üMass in gallbladder fossa
üLiver invasion
üNodal involvement
üDistant metastasis
GBC vs cholecystitis
Higher frequency of
• lymph node enlargement
• more extensive wall thickness
• focal irregularity
• less distension
LIMITATIONS
• Less helpful in differentiating between benign and
malignant polyps.
Computed tomography scan showing
gallbladder cancer with invasion into the
duodenum and liver parenchyma.
Computed tomography scan showing
gallbladder mass with local invasion into
portal vein (arrow).
MRI
• USG findings are confirmed on MRI.
MRI/MRCP – differentiate benign from malignant GB
lesions
• GBC is typically T1 hypointense and T2 hyperintense
compared with the surrounding liver parenchyma.
INDICATIONS – AS CECT
üMore accurate for imaging GB than extracorporeal
transabdominal US
üDetection and differential diagnosis of gallbladder
polyps and in staging tumor extent
üTo assess the depth of tumor invasion into the wall of
the gallbladder and for defining lymph node
involvement in the porta hepatis or peripancreatic
regions.
üMeans of obtaining bile for cytologic analysis and
EUS-guided FNA
ENDOSCOPIC ULTRASOUND
üCholangiography, ERCP and
percutaneous transhepatic
cholangiopancreatography
are of little use
üIn cases with jaundice, ERCP
may be necessary for
definition of the extent of
biliary involvement, as well as
for stent placement.
CHOLANGIOGRAPHY
ERCP in an adult with obstructive jaundice
demonstrates an APBDJ with malignant stricture
replacing the cystic duct insertion
üCECT CHEST – recommended
• Dstant metastases can affect the lungs and pleura
üPET / PET CT – not recommend
COMPLETING THE STAGING EVALUATION
• Generally nondiagnostic
• Elevated ALP or serum bilirubin - bile duct obstruction.
• Serum tumor markers – CEA or CA 19-9 are often elevated -
lack specificity and sensitivity .
If a tumor marker is found to be elevated preoperatively, serial assay after
resection might aid in the diagnosis of persistent or recurrent disease.
LABORATORY INVESTIGATIONS
Other non specific findings :
1. anemia
2. leukocytosis
3. transaminases elevation
4. ESR elevation
5. CRP Elevation
PATHOLOGY
INVASIVE ADENOCARCINOMA PRESENTING AS
MULTIFOCAL, NODULAR, PAPILLARY PROLIFERATION
IN THE FUNDUS & BODY OF GB
ADENOCARCINOMA PRESENTING AS DIFFUSE
THICKENING OF GB WALL
Incidental gallbladder adenocarcinoma
detected in a gallbladder with focal
thickening. A well differentiated
morphology.
Invasive papillary adenocarcinoma arising in
the background of an intracholecystic
papillary neoplasm.
HISTOPATHOLOGY
Gall Bladder Cancer – Incidental
Incidental
on
Histology
STAGING
GALL BLADDER CANCER - GROUPS
üObvious clinical
üSuspected imaging
üUnsuspected at operation
üIncidental at histology
üMissed at follow up
Kapoor. J HBP Surg 2007;14:366-73
PRIMARY TUMOUR STAGING
T stage T criteria
Tx Primary tumour cannot be assesed
T0 No evidence of primary tumour
T-is Carcinoma insitu
T 1 Tumour invades the lamina propria or muscular layer
T1a Tumour invades the lamina propria
T1b Tumour invades the muscular layer
T 2 Tumour invades the perimuscular connective tissue
T2 a Tumour invades the peri-muscular tissue on the peritoneal side
without involvement of the serosa(visceral peritoneum).
T2 b Tumour invades the perimuscular tissue on the hepatic side
without extension into the liver.
T3 Tumour perforates the serosa (visceral peritoneum) and/or
directly invades the liver and/or one other adjacent organ or
structures
T4 Tumour invades the main portal vein or hepatic artery or
invades two or more extra hepatic organs or structures.
REGIONAL NODE STAGING
N stage N criteria
Nx Regional lymph nodes cannot be
assessed
N0 No regional lymph node
metastasized
N1 Metastasis to 1 – 3 regional lymph
nodes
N2 Metastasis to 4 or more regional
lymph nodes.
METASTASIS
M stage M criteria
M0 No distant metastasis
M1 Distant metastasis
PROGNOSIS STAGE GROUP
T N M STAGE
Tis N0 M0 0
T1 N0 M0 I
T2a N0 M0 IIA
T2b N0 M0 IIB
T3 N0 M0 IIIA
T1-3 N1 M0 IIIB
T4 N0-1 M0 IVA
anyT N2 M0 IVB
anyT anyN M1 IVB
REFRENCES
Gall Bladder Cancer Diagnosis and Staging Guide

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Gall Bladder Cancer Diagnosis and Staging Guide

  • 1. DIAGNOSTIC EVALUATION & STAGING GALL BLADDER CARCINOMA SAMBHAVI JOSHI, 79, 2K17 Dr. ZAHID IQBAL MIR (SENIOR RESIDENT) MBBS, MS Surgery, DNB Surgery
  • 3. PATIENTS WITH SYMPTOMATIC CHOLELITHIASIS Screening – Ultrasound Additional cross-sectional imaging [CT, MRI/MRCP] in patients who have concerning findings on US • Calcification • a mass protruding into the lumen • loss of interface between gallbladder and liver • direct liver infiltration • gallbladder polyps ≥10 mm • thickened gallbladder wall not explained by cholecystitis
  • 4. USG vInitial diagnostic study for presumed gallbladder disease vOverall accuracy of USG for staging of GBC is limited
  • 5. USG FINDINGS - MALIGNANCY üMural thickening ücalcification ümass protruding into lumen üfixed mass in GB üloss of interface between gb and liver üdirect liver infiltration
  • 6. ØPolyp over 1 cm in diameter - invasive § FNAC (cholesterolosis/GBC) § Adenoma/GBC – less accurate § CT/MRI required ØPolyp less than 1 cm § adenoma/ papilloma/ cholesterosis/ GBC less likely COLOR DOPPLER - VASCULARITY • pulsatile flow - seen in most cases • continuous flow pattern • Doppler sensitivity is mandatory for diagnosis of GBC in stage T 1 a
  • 7. Ultrasound image showing intraluminal polypoid gallbladder wall mass (arrow) but without extraluminal extension. Ultrasound image of gallbladder mass with loss of continuity of gallbladder wall (arrow), suggesting extraluminal growth.
  • 8. Asymmetric gallbladder wall thickening (arrow) in a patient with GBC
  • 9. SUSPICIOUS ULTRASOUND FINDINGS OR INCIDENTAL GALLBLADDER CANCER AT CHOLECYSTECTOMY üPatients who have concerning findings on US - Evaluation of potential resectability is the key factor üIncidentally diagnosed GBC following simple cholecystectomy -Apropriate imaging (and detailed histopathologic analysis) is needed to decide whether further resection is necessary
  • 10. CECT • CT is more useful than US for detecting lymph node involvement, adjacent organ invasion, and distant metastasis. INDICATIONS • USG detected gallbladder lesion that may represent GBC • Incidentally diagnosed GBC following simple cholecystectomy.
  • 11. CT FINDINGS - GBC üPolypoid mass protruding into the lumen/ filling it üFocal or diffuse thickening of gallbladder wall. üMass in gallbladder fossa üLiver invasion üNodal involvement üDistant metastasis GBC vs cholecystitis Higher frequency of • lymph node enlargement • more extensive wall thickness • focal irregularity • less distension
  • 12. LIMITATIONS • Less helpful in differentiating between benign and malignant polyps. Computed tomography scan showing gallbladder cancer with invasion into the duodenum and liver parenchyma. Computed tomography scan showing gallbladder mass with local invasion into portal vein (arrow).
  • 13. MRI • USG findings are confirmed on MRI. MRI/MRCP – differentiate benign from malignant GB lesions • GBC is typically T1 hypointense and T2 hyperintense compared with the surrounding liver parenchyma. INDICATIONS – AS CECT
  • 14. üMore accurate for imaging GB than extracorporeal transabdominal US üDetection and differential diagnosis of gallbladder polyps and in staging tumor extent üTo assess the depth of tumor invasion into the wall of the gallbladder and for defining lymph node involvement in the porta hepatis or peripancreatic regions. üMeans of obtaining bile for cytologic analysis and EUS-guided FNA ENDOSCOPIC ULTRASOUND
  • 15. üCholangiography, ERCP and percutaneous transhepatic cholangiopancreatography are of little use üIn cases with jaundice, ERCP may be necessary for definition of the extent of biliary involvement, as well as for stent placement. CHOLANGIOGRAPHY ERCP in an adult with obstructive jaundice demonstrates an APBDJ with malignant stricture replacing the cystic duct insertion
  • 16. üCECT CHEST – recommended • Dstant metastases can affect the lungs and pleura üPET / PET CT – not recommend COMPLETING THE STAGING EVALUATION
  • 17. • Generally nondiagnostic • Elevated ALP or serum bilirubin - bile duct obstruction. • Serum tumor markers – CEA or CA 19-9 are often elevated - lack specificity and sensitivity . If a tumor marker is found to be elevated preoperatively, serial assay after resection might aid in the diagnosis of persistent or recurrent disease. LABORATORY INVESTIGATIONS Other non specific findings : 1. anemia 2. leukocytosis 3. transaminases elevation 4. ESR elevation 5. CRP Elevation
  • 18. PATHOLOGY INVASIVE ADENOCARCINOMA PRESENTING AS MULTIFOCAL, NODULAR, PAPILLARY PROLIFERATION IN THE FUNDUS & BODY OF GB ADENOCARCINOMA PRESENTING AS DIFFUSE THICKENING OF GB WALL
  • 19. Incidental gallbladder adenocarcinoma detected in a gallbladder with focal thickening. A well differentiated morphology. Invasive papillary adenocarcinoma arising in the background of an intracholecystic papillary neoplasm. HISTOPATHOLOGY
  • 20. Gall Bladder Cancer – Incidental Incidental on Histology
  • 21.
  • 23. GALL BLADDER CANCER - GROUPS üObvious clinical üSuspected imaging üUnsuspected at operation üIncidental at histology üMissed at follow up Kapoor. J HBP Surg 2007;14:366-73
  • 24. PRIMARY TUMOUR STAGING T stage T criteria Tx Primary tumour cannot be assesed T0 No evidence of primary tumour T-is Carcinoma insitu T 1 Tumour invades the lamina propria or muscular layer T1a Tumour invades the lamina propria T1b Tumour invades the muscular layer T 2 Tumour invades the perimuscular connective tissue T2 a Tumour invades the peri-muscular tissue on the peritoneal side without involvement of the serosa(visceral peritoneum). T2 b Tumour invades the perimuscular tissue on the hepatic side without extension into the liver. T3 Tumour perforates the serosa (visceral peritoneum) and/or directly invades the liver and/or one other adjacent organ or structures T4 Tumour invades the main portal vein or hepatic artery or invades two or more extra hepatic organs or structures.
  • 25.
  • 26. REGIONAL NODE STAGING N stage N criteria Nx Regional lymph nodes cannot be assessed N0 No regional lymph node metastasized N1 Metastasis to 1 – 3 regional lymph nodes N2 Metastasis to 4 or more regional lymph nodes. METASTASIS M stage M criteria M0 No distant metastasis M1 Distant metastasis
  • 27. PROGNOSIS STAGE GROUP T N M STAGE Tis N0 M0 0 T1 N0 M0 I T2a N0 M0 IIA T2b N0 M0 IIB T3 N0 M0 IIIA T1-3 N1 M0 IIIB T4 N0-1 M0 IVA anyT N2 M0 IVB anyT anyN M1 IVB