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1)  cystic odontoma
囊性牙瘤
2)  keratocystic odontogenic tumour
牙源性角化囊性瘤
1.
The odontogenic keratocyst(OKC)is reclassified as the keratocystic odontogenic tumour(KCOT)by the World Health Organization(WHO)based on the well-known aggressive behaviour of this lesion,its histology and new information regarding its genetics.
牙源性角化囊肿(odontogenic keratocyst,OKC)因其侵袭性行为、组织学和遗传学方面的新发现,在WHO的分类中已命名为牙源性角化囊性瘤(keratocystic odontogenic tumour,KCOT)。
3)  keratocystic odontogenic tumor
牙源性角化囊性瘤
1.
Odontogenic keratocyst (OKC) is characterized by its high recurrence rate,aggressive behavior,and occasional association with basal cell nevus syndrome,which is now designated by the World Health Organization (WHO) as a keratocystic odontogenic tumor (KCOT).
牙源性角化囊性瘤原称牙源性角化囊肿,因其生长缺乏自限性,具有某些肿瘤的特征,术后有较高复发倾向,WHO将其归属为良性牙源性肿瘤,并命名为牙源性角化囊性瘤。
4)  Multiple primary keratocystic odontogenic tumor(MPKCOT)
多原发性牙源性角化囊性瘤
5)  Asynchronous symmetrical multiple primary keratocystic odontogenic tumor
异时对称多原发性牙源性角化囊性瘤
6)  odontogenic tumor
牙原性瘤
补充资料:先天性囊性纤维性骨炎综合征及棕色素斑综合征


先天性囊性纤维性骨炎综合征及棕色素斑综合征


病名。即多发性骨纤维结构不良综合征。详见该条。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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