Beruflich Dokumente
Kultur Dokumente
MASS LIVER
NON-NEOPLASTIC NEOPLASTIC
BENIGN
MALIGNANT
NON-NEOPLASTIC LESIONS
CYSTS - POLYCYSTIC DISEASE. - CAROLIS DISEASE. FOCAL NODULAR HYPERPLASIA. NODULAR REGENERATIVE HYPERPLASIA. BILIARY HAMARTOMA. PELIOSIS HEPATIS. HYDATID CYST. AMEOBIC ABSCESS . TUBERCULOMA.
BENIGN TUMORS
EPITHELIAL . 1) HEPATIC ADENOMA. 2) BILE DUCT ADENOMA. NON-EPITHELIAL. 1) HEMANGIOMA. 2) LYMPHANGIOMA.
MALIGNANT TUMORS
EPITHELIAL. NON-EPITHELIAL. 1)HEPATOCELLULAR 1)ANGIOSARCOMA. CARCINOMA. 2)RHABDOMYOSAR 2)HEPATOBLASTOMA. COMA. 3)BILE DUCT CA. 3)LYMPHOMA. 4)HILAR ADENOCA. (KLATSKIN TUMOR) METASTATIC.
POLYCYSTIC LIVER
CAROLIS DISEASE
CAROLIS DISEASE
HYDATID CYST
HYDATID CYST
HYDATID CYST
AMOEBIC ABSCESS
PELIOSIS HEPATIS
HEPATIC ADENOMA
ADENOMA
ORAL CONTRACEPTIVES. MIMIC CARCINOMA. PERITONEAL RUPTURE. HCC ARISE RARELY.
ADENOMA
ADENOMA - MICRO
SHEETS & CORDS OF HEPATOCYTES 2 3 CELLS THICK SEPARATED BY SINUSOIDS. PORTAL TRACTS ABSENT.
CAVERNOUS HEMANGIOMA
HEPATOCELLULAR CARCINOMA
HEPATOCELLULAR CA
HEPATOCELLULAR CA
M : F 3 : 1. 7TH COMMON IN MALE. 9TH COMMON IN FEMALE. OLDER AGE > 60 IN CIRRHOTIC LIVER. 20 40 YRS IN HEPATITIS PATIENTS.
ETIOPATHOLOGY
GENETIC - NO CONVINCING EVIDENCE. - ASSOSIATED WITH FAMILIAL POLYPOSIS COLI, ATAXIA TELANGIECTASIA.
AGE
OLDER AGE YOUNG AGE - ALCOHOLIC. - HEPATITIS.
SEX
MALE
> FEMALE.
METABOLIC
TYROSINEMIA. ALPHA I ANTITRYPSIN DEFICIENCY. PRIMARY IDIOPATHIC HEMOCHROMATOSIS. WILSONS DISEASE . GLYCOGEN STORAGE DISORDERS.
HEMOCHROMATOSIS
NUTRITION
OVERNUTRITION.
CARCINOGEN
AFLATOXIN. NITROSAMINE. TANNIC ACID. CYCASIN.
CIRRHOSIS - 10 15 % RISK.
VIRAL HEPATITIS
HEPATITIS- B . HEPATITIS- C.
CIRRHOSIS
HBV , HCV
ALCOHOL HEMOCHROMATOSIS
OTHERS
HIGH RISK
INTERMEDIATE RISK
LOW RISK
HYPERPLASIA , DYSPLASIA
CARCINOMA
CLINICAL FEATURES
UPPER ABDOMINAL MASS / PAIN. MALAISE , FATIGUE, WT LOSS. JAUNDICE , FEVER, ASCITES, ENCEPHALOPATHY. ESOPHAGEAL VARICEAL BLEED. BUDD CHIARI SYNDROME. METASTASIS.
INVESTIGATIONS
SERUM ALPHA FETO PROTEIN. - 100 200 ng /ml HEPATITIS. - > 500 ng / ml HEPATOMA. SERUM CEA. USG. ANGIOGRAPHY. CT / MRI. BIOPSY.
PARANEOPLASTIC SYNDROME
HYPOGLYCEMIA. ERYTHROCYTOSIS. HYPERCALCEMIA. HYPERCHOLESTEROLEMIA.
FINAL OUTCOME
HEPATIC FAILURE. GI BLEED. RUPTURE IN TO PERITONEUM. CACHEXIA.
MORPHOLOGY
GROSS. EGGEL CLASSIFICATION. 1) UNIFOCAL. 2) MULTIFOCAL. 3) DIFFUSE.
MICROSCOPIC
WELL DIFFERENTIATED. - TRABECULAR. - ACINAR. - SOLID. ANAPLASTIC.
FIBROLAMELLAR CARCINOMA
YOUNG AGE 20 40 YRS. F > M. BETTER PROGNOSIS. NO ASSOCIATION WITH HBV OR CIRRHOSIS.
TREATMENT
SURGICAL RESECTION. INJECTION OF ALCOHOL. CHEMOEMBOLISM. RADIATION. TRANSPLANTATION.
HEPATOBLASTOMA
HEPATOBLASTOMA
0.2 5 % OF CHILDHOOD TUMORS. 25 45 % OF PRIMARY HEPATIC TUMORS. 83 92 % OCCURS IN < 5 YRS OF AGE. 66 % IN < 2 YRS . M > F.
ASSOCIATIONS
HEMIHYPERTROPHY. DOWN SYNDROME. NEPHROBLASTOMA. FAP SYNDROME.
CLINICAL FEATURES
FAILURE TO THRIVE. LOSS OF WT. ABDOMINAL MASS. JAUNDICE. ELEVATED HCG. ELEVATED AFP.
MICROSCOPY
EPITHELIAL. MESENCHYMAL. MIXED.
CHOLANGIOCARCINOMA
OLDER AGE. CLONORCHIS SINENSIS. NITROSAMINES. HEPATOLITHIASIS. CAROLIS DISEASE. CHOLEDOCHAL CYST.
ANGIOSARCOMA
VINYL CHLORIDE, ARSENIC, THOROTHRAST.
METASTASIS
SUMMARY