Klippel-trenaunay syndrome: A pedodontist perspective

Topi Nyodu, Soumen Pal, Khooshbu Gayen, P. Nanmaran, S. Sarkar
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Abstract

Klippel–Trenaunay syndrome (KTS) is a congenital, uncommon but a well-recognized disorder, characterized by cutaneous hemangiomas, varicosities, and unilateral bone and soft tissue hypertrophy with different localization. Generally diagnosed at birth or first few years of life. KTS represents a syndrome of interest for those in the field of oral and maxillofacial radiology and pathology because of high incidence of variations seen in the orofacial region in affected patients. A case of a 3-year-old female patient with KTS reported to the Department of Pedodontics and Preventive Dentistry for extraction, and we have documented and tabulated the Orodental manifestation of this patient.
可以做一个追踪装置
klipppel - trenaunay综合征(KTS)是一种罕见但公认的先天性疾病,以皮肤血管瘤、静脉曲张、单侧骨和软组织肥大为特征。一般在出生或生命最初几年被诊断出来。KTS代表了口腔颌面放射学和病理学领域感兴趣的综合征,因为在受影响的患者中,口面部区域的变异发生率很高。一例3岁的KTS女性患者报告到儿科和预防牙科拔牙,我们记录并列出了该患者的东方学表现。
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