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Angiofollicular lymph node hyperplasia
Angiofollicular lymphoid hyperplasia
Angiomatous lymphoid
Burkitt's tumour
Castleman disease
Castleman syndrome
Castleman tumor
Castleman's disease
Castleman's lymphoma
Castleman's syndrome
Castleman's tumour
Craniopharyngioma
Ewing family of tumours
Ewing sarcoma
Ewing tumor
Ewing tumour
Ewing's sarcoma
Ewing's tumor
Ewing's tumour
Excision of a cancerous tumour
Excision of a tumour
GLNH
Giant benign lymphoma
Giant lymph node hyperplasia
Hamartoma of the lymphatics
Rathke's pouch tumor
Rathke's pouch tumour
Rathke's tumor
Rathke's tumour

Traduction de «Castleman's tumour » (Anglais → Français) :

Castleman's disease | giant lymph node hyperplasia | GLNH | giant benign lymphoma | hamartoma of the lymphatics | Castleman tumor | Castleman's tumour | Castleman's lymphoma | angiofollicular lymphoid hyperplasia | angiofollicular lymph node hyperplasia | angiomatous lymphoid | Castleman's syndrome

maladie de Castleman | hyperplasie angiofolliculaire | tumeur de Castleman | lymphome de Castleman | hyperplasie ganglionnaire angiofolliculaire | hyperplasie lymphoïde angiofolliculaire | hyperplasie ganglionnaire géante | hamartome lymphoïde | lymphome bénin | lymphoréticulome folliculaire | syndrome de Castleman


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

craniopharyngiome | adamantinome | tumeur de la poche de Rathke


Ewing sarcoma | Ewing's sarcoma | Ewing tumor | Ewing tumour | Ewing's tumor | Ewing's tumour

sarcome d'Ewing | tumeur d'Ewing


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

famille des tumeurs d’Ewing | tumeur d'Ewing






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


excision of a cancerous tumour | excision of a tumour

excision d'une tumeur cancéreuse


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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