Yuzi Kamiya, Hidetaka Narita, Tadashi Yamamoto, Yoichiro Kameyama , Hatsuhiko Maeda, Satoshi Nakane
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引用次数: 6

摘要

本报告描述家族性牙源性角化囊肿。病例1患者有3个姐妹,发生牙源性角化囊肿。2个妹妹(病例2和3)也有牙源性角化囊肿,尽管姐姐没有任何牙源性囊肿。患者的父亲有颌囊肿切除史,母亲后来被发现患有恶性成釉细胞瘤。除牙源性角化囊肿外,病例1还伴有基底细胞痣、额突突出和远视;病例2患者额突突出;病例3患者有突出的额突、远视和斜视。三姐妹均怀疑为基底细胞痣综合征患者。本文回顾了日本有关基底细胞痣综合征的牙科文献。
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Familial odontogenic keratocysts

Familial odontogenic keratocysts are described in this report. The Case 1 patient, who has 3 sisters, developed odontogenic keratocysts. The 2 younger sisters (Cases 2 and 3) also had odontogenic keratocysts, although the elder sister did not have any odontogenic cysts. The father of the patients had a history of removal of a jaw cyst, and the mother was found later to have malignant ameloblastoma. Besides the odontogenic keratocysts, the Case 1 patient had basal cell nevus, prominent frontal process, and ocular hypertelorism; the Case 2 patient had prominent frontal process; the Case 3 patient had prominent frontal process, ocular hypertelorism, and squint. All 3 sisters are suspected of being patients with the basal cell nevus syndrome. The Japanese dental literature concerning the basal cell nevus syndrome is reviewed.

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