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Benign neoplasm
Benign neoplastic disease
Benign tumor
Benign tumour
Cancer of the colon and rectum
Colon and rectum cancer
Colorectal cancer
Highly aggressive neoplasm
Malignant neoplasm of rectum
Neoplasm
Neoplasm of rectum
Non-malignant tumor
Per rectum
Rectally
Through the rectum
Tumor
Tumour

Translation of "neoplasm rectum " (English → French) :

colorectal cancer | colon and rectum cancer | cancer of the colon and rectum

cancer colorectal | cancer rectocolique | cancer du côlon et du rectum
médecine > oncologie | médecine > gastroentérologie
médecine > oncologie | médecine > gastroentérologie


per rectum | rectally | through the rectum

par voie rectale
IATE - Health
IATE - Health


Neoplasm of rectum

tumeur du rectum
SNOMEDCT-BE (disorder) / 126847008
SNOMEDCT-BE (disorder) / 126847008


Malignant neoplasm of rectum

Tumeur maligne du rectum
WORLD HEALTH ORGANIZATION ICD-10: C20
WORLD HEALTH ORGANIZATION ICD-10: C20


tumor | tumour | neoplasm

tumeur | néoplasme | néoformation | néoplasie
médecine > anatomopathologie
médecine > anatomopathologie


benign tumor | benign tumour | benign neoplasm | non-malignant tumor | benign neoplastic disease

tumeur bénigne | néoplasme bénin | tumeur simple
médecine > oncologie
médecine > oncologie


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


highly aggressive neoplasm

néoplasie extrêmement agressive
IATE - Health
IATE - Health


neoplasm | tumour

néoplasme | tumeur
IATE - Health
IATE - Health


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




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'neoplasm rectum'

Date index:2022-07-18 -

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