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Craniopharyngioma
Endodermal sinus tumor
Endodermal sinus tumour
Ewing family of tumours
Ewing tumour
Ewing's tumour
Exophytic
Exophytic lesion
Exophytic tumour
NSGCT
NSTGCT
Nonseminoma
Nonseminomatous germ cell tumor
Nonseminomatous germ cell tumour
Nonseminomatous testicular germ cell tumor
Nonseminomatous testicular germ cell tumour
Nonseminomatous testicular tumor
Nonseminomatous testicular tumour
Nonseminomatous tumor
Nonseminomatous tumour
Rathke's pouch tumor
Rathke's pouch tumour
Rathke's tumor
Rathke's tumour
Yolk sac carcinoma
Yolk sac tumor
Yolk sac tumour

Traduction de «exophytic tumour » (Anglais → Français) :



A rare subtype of mixed epithelial-mesenchymal tumour, often presenting as a large, exophytic polypoid lesion, which may extend through the cervix, composed of benign or atypical epithelium and low-grade malignant stroma. It usually presents with dys

adénosarcome du corps de l'utérus


nonseminomatous germ cell tumor | NSGCT | nonseminomatous germ cell tumour | nonseminomatous testicular germ cell tumor | NSTGCT | nonseminomatous testicular germ cell tumour | nonseminomatous testicular tumor | nonseminomatous testicular tumour | nonseminomatous tumor | nonseminomatous tumour | nonseminoma

tumeur germinale non séminomateuse | TGNS | tumeur non séminomateuse | TNS


Ewing family of tumours | Ewing tumour | Ewing's tumour

famille des tumeurs d’Ewing | tumeur d'Ewing




endodermal sinus tumor | endodermal sinus tumour | yolk sac tumor | yolk sac tumour | yolk sac carcinoma

tumeur vitelline | tumeur du sac vitellin | tumeur du sinus endodermique


craniopharyngioma | Rathke's pouch tumour | Rathke's pouch tumor | Rathke's tumour | Rathke's tumor

craniopharyngiome | adamantinome | tumeur de la poche de Rathke




An extremely rare tumour association characterised by dual predisposition to melanoma and neural system tumours (typically astrocytoma). Fewer than 20 affected families have been reported to date. Affected individuals had cutaneous melanoma in associ

syndrome mélanome-tumeur du système nerveux


A rare hepatic tumour that may manifest with abdominal pain or fullness, as well as diarrhoea or weight loss. More than 10% of cases are asymptomatic and in rare cases a carcinoid syndrome may be observed. The age of onset is variable. The aetiology

carcinome neuroendocrine hépatique primaire


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