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HEPATOCELLULAR 
CARCINOMA 
WE CAN CHANGE THE OUTCOME
Background 
 The incidence of hepatocellular carcinoma (HCC) has 
continued to rise in recent years. 
 This increase has been attributed to alcohol-induced 
liver diseases, metabolic syndrome, and the rising 
number of hepatitis B and C viral infections. 
 Treatment options are evolving. With better 
understanding of liver anatomy and physiology surgical 
treatment emerges as the main curative option
Case Discussion 
 68 years old male, Diabetic/ hypertensive/ IHD ( on medical 
management) 
 RUQ discomfort - 2-3 months 
 generalized weakness, fatigue, exertional breathlessness 
 No addictions, No H/O hepatitis infection. 
 GPE - pallor ++, BMI-35, otherwise normal, good performance 
status 
 Abdomen examination– unremarkable
Investigations 
 Hb – 6.6 gm % - transfused 2 PRC’s. 
 PS –Normocytic hypochromic aneamia 
 Platelets-3.2 lakhs 
 INR-1.21 
 LFT bil-1.2,alb 3.3 OT/PT-56/67 
 Iron , B12 low 
 Viral markers negative 
 Echo, ECG - normal
Investigations 
 UGI scopy – normal study of stomach 
 Colonoscopy – small Haemorrhoids. Occasional 
uncomplicated left colonic diverticulae + 
 CT abdomen – for evaluation of bleeding
NON CONTRAST CT
CT : ARTERIAL PHASE
CT: PORTAL VENOUS PHASE
CT: EQUILIBRIUM PHASE
DDs for liver SOL 
 Can you characterise liver lesions on imaging?
IMAGING OF HEPATOMAS 
USG, CT, MRI
ULTRASONOGRAPHY IN HEPATOMA
CT OF HEPATOMA
VALUE OF MRI IN HEPATOMA 
SIDEROTIC NODULE – appears black 
Dyplastic nodule: 
NO ARTERIAL PHASE ENHANCEMENT 
HEPATOMA: ARTERIAL PHASE ENHANCEMENT
Differentiation from other solid liver lesions 
Focal Nodular Hyperplasia
HepaticAdenoma 
Sub capsular feeding artery 
Thin capsule with delayed enhancement.
Hemangioma
Further Evaluation ? 
 Tumour markers 
 AFP – 423 IU/dl 
 DCP/CEA/CA 19 9 - normal 
 ?Biopsy 
 Decision on curative treatment
Biopsy – to do or not to do!!!!! 
 Risk of biopsy in liver tumors: 
 False negative – targetting error 
 Bleeding 
 Intrahepatic dissemination 
 Peritoneal dissemination 
 When to biopsy?? 
 Resectable lesion – NO BIOPSY 
 Typical radiological features +/- raised AFP – NO BIOPSY 
 Atypical radiological features + raised AFP – NO BIOPSY 
 Atypical radiological features + normal AFP + nonresectable - BIOPSY
How to manage this case ? 
Diagnosis conformed by Imaging and AFP
Treatment Options for HCC 
Surgical Resection 
Open 
Laparoscopic 
Liver Transplantation 
Local Ablative Therapies 
RFA 
PEI 
Microwave etc 
Regional Therapy 
Multimodality therapy 
TACE 
Theraspheres 
Hepatic arterial infusion 
Systemic chemotherapy 
Radiation therapy 
Cyberknife
Treatment of HCC
Which patients should undergo resection? 
Performance status 
Associated Medical Diseases 
Stage of Disease 
Size /Number of lesions 
Extrahepatic disease 
Portal vein status 
Functional hepatic reserve
What resection and how much to 
resect
HCC- Child’s A Cirrhosis
Radiological Assessment? 
 Virtual Surgery 
 Volumetry of the Liver to assess for 
residual liver or future liver remnant (FLR)
HOW CAN TECHNOLOGY 
HELP ? 
ADVANCED CT IMAGING TECHNIQUES.
TOTAL LIVER VOLUME: 1256 CC 
RESIDUAL LIVER VOLUME: 1256- 
440CC = 816CC 
PERCENTAGE 
RESIDUAL LIVER 
VOLUME = 64%
TOTAL LIVER VOLUME: 1256 CC 
TUMOR VOLUME = 220 CC 
TOTAL FUNCTIONAL LIVER VOLUME = 1256-220: 
1036 CC 
RESIDUAL LIVER VOLUME: 1036-440 = 596 CC. 
PERCENTAGE RESIDUAL 
LIVER VOLUME = 
596 / 1036 : 57%
Assessment 
 Patient – Good performance status, fit for surgery; medical 
factors well controlled 
 Disease related – Localised disease; no evidence of spread 
 Liver Status –rt Posterior sectionectomy, Segment 6,7; Good 
residual volume 
 Facilities – Intraoperative USG; Dissecting tools – Waterjet; 
Hemostatic tools – harmonic and Aquamantys 
 Surgeon and team
Armamentarium
Right post sectionectomy for this 
patient
Post operative Course 
No major morbidity 
 Discharged on Day 6 
 Follow up- doing well
FNAC OR BIOPSY FOR DIAGNOSIS? 
 Malignant tumours of liver can be confidently 
diagnosed on FNAC. However, FNAC has limitations 
and diagnostic challenges in benign lesions and well-differentiated 
HCC. 
 Biopsy allows architectural, cellular and 
immunohistochemical evaluation. 
 A combined approach of biopsy with clinical findings, 
tumour markers and ancillary techniques is preferred.
Microscopy 
MICROACINAR 
PATTERN 
HYALINE GLOBULES WITH POORLY 
DIFFERENTIATED CELLS
Results of Biopsy in Suspected HCC 
 Sensitivity of FNA 67-100% 
 Specificity of FNA 80-100% 
 Risk of needle track seeding 2.7% overall, 0.9%/year 
 Median time for seeding: 17/12 (3-48/12) 
Silva MA et al.Gut 2008;57:1592-1596
Pathology of HCC 
 Histopathology of this patient 
 Prognostic factors
Histology of HCC 
 Well-differentiated HCCs are those where the tumour 
cells closely resemble hepatocytes. 
 Poorly differentiated HCC are those where the 
hepatocellular nature of the tumour is not 
very evident from the morphology.
CORE DATA ITEMS IN PATHOLOGY REPORT 
 Size 
 Number 
 Grade 
 Vascular invasion 
 Capsular invasion 
 Resection margin 
 Type (fibrolamellar variant better prognosis) 
 Background liver 
 Lymph node status
Outcome of Surgery 
 Good risk patient(Non Cirrhotic, Child A CLD) 
 Disease Status 
 Surgical expertise 
 Strict intra op measures – monitoring, less blood loss 
 Good residual liver volume 
 Complete resection with good margin 
 Favourable pathology
Take home messages 
 HCC - increasing diagnosis due to awareness 
 Should be evaluated by an experienced team –to select 
the best treatment option for increased chance of cure 
 Do not needle all liver lesions! 
 Age and size of tumour really do not necessarily rule out 
curative surgery 
 A meticulously planned surgery with intraoperative and 
perioperative care results in excellent outcome 
 Treatment should be undertaken at center’s with 
experience and facilities
THANK YOU

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Grish hcc presentation

  • 1. HEPATOCELLULAR CARCINOMA WE CAN CHANGE THE OUTCOME
  • 2.
  • 3. Background  The incidence of hepatocellular carcinoma (HCC) has continued to rise in recent years.  This increase has been attributed to alcohol-induced liver diseases, metabolic syndrome, and the rising number of hepatitis B and C viral infections.  Treatment options are evolving. With better understanding of liver anatomy and physiology surgical treatment emerges as the main curative option
  • 4. Case Discussion  68 years old male, Diabetic/ hypertensive/ IHD ( on medical management)  RUQ discomfort - 2-3 months  generalized weakness, fatigue, exertional breathlessness  No addictions, No H/O hepatitis infection.  GPE - pallor ++, BMI-35, otherwise normal, good performance status  Abdomen examination– unremarkable
  • 5. Investigations  Hb – 6.6 gm % - transfused 2 PRC’s.  PS –Normocytic hypochromic aneamia  Platelets-3.2 lakhs  INR-1.21  LFT bil-1.2,alb 3.3 OT/PT-56/67  Iron , B12 low  Viral markers negative  Echo, ECG - normal
  • 6. Investigations  UGI scopy – normal study of stomach  Colonoscopy – small Haemorrhoids. Occasional uncomplicated left colonic diverticulae +  CT abdomen – for evaluation of bleeding
  • 11.
  • 12. DDs for liver SOL  Can you characterise liver lesions on imaging?
  • 13. IMAGING OF HEPATOMAS USG, CT, MRI
  • 16. VALUE OF MRI IN HEPATOMA SIDEROTIC NODULE – appears black Dyplastic nodule: NO ARTERIAL PHASE ENHANCEMENT HEPATOMA: ARTERIAL PHASE ENHANCEMENT
  • 17. Differentiation from other solid liver lesions Focal Nodular Hyperplasia
  • 18. HepaticAdenoma Sub capsular feeding artery Thin capsule with delayed enhancement.
  • 20. Further Evaluation ?  Tumour markers  AFP – 423 IU/dl  DCP/CEA/CA 19 9 - normal  ?Biopsy  Decision on curative treatment
  • 21. Biopsy – to do or not to do!!!!!  Risk of biopsy in liver tumors:  False negative – targetting error  Bleeding  Intrahepatic dissemination  Peritoneal dissemination  When to biopsy??  Resectable lesion – NO BIOPSY  Typical radiological features +/- raised AFP – NO BIOPSY  Atypical radiological features + raised AFP – NO BIOPSY  Atypical radiological features + normal AFP + nonresectable - BIOPSY
  • 22. How to manage this case ? Diagnosis conformed by Imaging and AFP
  • 23. Treatment Options for HCC Surgical Resection Open Laparoscopic Liver Transplantation Local Ablative Therapies RFA PEI Microwave etc Regional Therapy Multimodality therapy TACE Theraspheres Hepatic arterial infusion Systemic chemotherapy Radiation therapy Cyberknife
  • 25. Which patients should undergo resection? Performance status Associated Medical Diseases Stage of Disease Size /Number of lesions Extrahepatic disease Portal vein status Functional hepatic reserve
  • 26. What resection and how much to resect
  • 27.
  • 28.
  • 29.
  • 30. HCC- Child’s A Cirrhosis
  • 31. Radiological Assessment?  Virtual Surgery  Volumetry of the Liver to assess for residual liver or future liver remnant (FLR)
  • 32. HOW CAN TECHNOLOGY HELP ? ADVANCED CT IMAGING TECHNIQUES.
  • 33.
  • 34. TOTAL LIVER VOLUME: 1256 CC RESIDUAL LIVER VOLUME: 1256- 440CC = 816CC PERCENTAGE RESIDUAL LIVER VOLUME = 64%
  • 35. TOTAL LIVER VOLUME: 1256 CC TUMOR VOLUME = 220 CC TOTAL FUNCTIONAL LIVER VOLUME = 1256-220: 1036 CC RESIDUAL LIVER VOLUME: 1036-440 = 596 CC. PERCENTAGE RESIDUAL LIVER VOLUME = 596 / 1036 : 57%
  • 36. Assessment  Patient – Good performance status, fit for surgery; medical factors well controlled  Disease related – Localised disease; no evidence of spread  Liver Status –rt Posterior sectionectomy, Segment 6,7; Good residual volume  Facilities – Intraoperative USG; Dissecting tools – Waterjet; Hemostatic tools – harmonic and Aquamantys  Surgeon and team
  • 38.
  • 39. Right post sectionectomy for this patient
  • 40. Post operative Course No major morbidity  Discharged on Day 6  Follow up- doing well
  • 41. FNAC OR BIOPSY FOR DIAGNOSIS?  Malignant tumours of liver can be confidently diagnosed on FNAC. However, FNAC has limitations and diagnostic challenges in benign lesions and well-differentiated HCC.  Biopsy allows architectural, cellular and immunohistochemical evaluation.  A combined approach of biopsy with clinical findings, tumour markers and ancillary techniques is preferred.
  • 42. Microscopy MICROACINAR PATTERN HYALINE GLOBULES WITH POORLY DIFFERENTIATED CELLS
  • 43. Results of Biopsy in Suspected HCC  Sensitivity of FNA 67-100%  Specificity of FNA 80-100%  Risk of needle track seeding 2.7% overall, 0.9%/year  Median time for seeding: 17/12 (3-48/12) Silva MA et al.Gut 2008;57:1592-1596
  • 44. Pathology of HCC  Histopathology of this patient  Prognostic factors
  • 45. Histology of HCC  Well-differentiated HCCs are those where the tumour cells closely resemble hepatocytes.  Poorly differentiated HCC are those where the hepatocellular nature of the tumour is not very evident from the morphology.
  • 46. CORE DATA ITEMS IN PATHOLOGY REPORT  Size  Number  Grade  Vascular invasion  Capsular invasion  Resection margin  Type (fibrolamellar variant better prognosis)  Background liver  Lymph node status
  • 47. Outcome of Surgery  Good risk patient(Non Cirrhotic, Child A CLD)  Disease Status  Surgical expertise  Strict intra op measures – monitoring, less blood loss  Good residual liver volume  Complete resection with good margin  Favourable pathology
  • 48. Take home messages  HCC - increasing diagnosis due to awareness  Should be evaluated by an experienced team –to select the best treatment option for increased chance of cure  Do not needle all liver lesions!  Age and size of tumour really do not necessarily rule out curative surgery  A meticulously planned surgery with intraoperative and perioperative care results in excellent outcome  Treatment should be undertaken at center’s with experience and facilities