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Encephalopathy NOS
Fulminant
Hepatic coma NOS
Hepatitis acute
Hepatocellular
Hepatotoxic
Liver cell carcinoma
Liver cell-related
Malignant
Poisonous to liver cells
Squamous cell carcinoma of auricle

Translation of "liver cell carcinoma " (English → French) :

Liver cell carcinoma

Carcinome hépatocellulaire
WORLD HEALTH ORGANIZATION ICD-10: C22.0
WORLD HEALTH ORGANIZATION ICD-10: C22.0


Squamous cell carcinoma of liver and intrahepatic biliary tract is an extremely rare primary malignant liver and biliary tract epithelial neoplasm originating in the intrahepatic bile duct epithelium histologically characterized by the presence of ke

carcinome épidermoïde du foie et des voies biliaires intrahépatiques
SNOMEDCT-BE (disorder) / 770684008
SNOMEDCT-BE (disorder) / 770684008


A rare slow-growing uterine cancer with histological characteristics of small, well differentiated nests of basaloid cells resembling basal cell carcinoma of the skin, commonly associated with squamous cell carcinoma or squamous intraepithelial lesio

carcinome adénoïde basal du col de l'utérus
SNOMEDCT-BE (disorder) / 763063001
SNOMEDCT-BE (disorder) / 763063001


hepatic:coma NOS | encephalopathy NOS | hepatitis:acute | fulminant | malignant | NEC, with hepatic failure | liver (cell) necrosis with hepatic failure yellow liver atrophy or dystrophy

atrophie ou dystrophie jaune du foie coma | encéphalopathie | hépatique SAI | hépatite:aiguë | fulminante | maligne | NCA, avec insuffisance hépatique | nécrose des hépatocytes avec insuffisance hépatique
WORLD HEALTH ORGANIZATION ICD-10: K72
WORLD HEALTH ORGANIZATION ICD-10: K72


hepatocellular | liver cell-related

hépato-cellulaire | qui affecte les cellules du foie
UGENT - Medical terms -
UGENT - Medical terms -


hepatotoxic | poisonous to liver cells

hépatotoxique | toxique pour le foie
UGENT - Medical terms -
UGENT - Medical terms -


A hereditary renal cancer syndrome defined as development of hereditary clear cell renal cell carcinoma (ccRCC) in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other neoplasm p

carcinome rénal héréditaire à cellules claires
SNOMEDCT-CA (ccRCC) in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other neoplasm p / 764961009
SNOMEDCT-CA (trouble) / 764961009


A rare epithelial tumor of the colon arising from squamous cells of the colorectal epithelium without the presence of squamous-lined fistulous tracts or a proximal extension of an anal squamous cell carcinoma. It usually presents with nonspecific sym

carcinome épidermoïde du côlon
SNOMEDCT-BE (disorder) / 766981007
SNOMEDCT-BE (disorder) / 766981007


A rare epithelial tumor of the rectum, arising from squamous cells in the rectal epithelium, without the presence of squamous-lined fistulous tracts in the rectum or a proximal extension of squamous cell carcinoma of anal or gynecological origin. The

carcinome épidermoïde du rectum
SNOMEDCT-BE (disorder) / 766979005
SNOMEDCT-BE (disorder) / 766979005


Squamous cell carcinoma of auricle

carcinome épidermoïde de l'auricule d'une oreille
SNOMEDCT-BE (disorder) / 423700001
SNOMEDCT-BE (disorder) / 423700001




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'liver cell carcinoma'

Date index:2021-07-11 -

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