智力发育迟缓-过度生长（辛普森-戈拉比-贝梅尔）综合征中的多发性牙源性角化囊肿

Multiple odontogenic keratocysts in mental retardation-overgrowth (Simpson-Golabi-Behmel) syndrome.

作者信息

Krimmel M, Reinert S

机构信息

Department of Oral and Maxillofacial Surgery, University of Tübingen, Tübingen, Germany.

出版信息

Br J Oral Maxillofac Surg. 2000 Jun;38(3):221-3. doi: 10.1054/bjom.1999.0186.

DOI:10.1054/bjom.1999.0186

PMID:10864729

Abstract

We report on a 10-year-old boy with mental retardation-overgrowth (Simpson-Golabi-Behmel) syndrome. The child had the typical clinical features including, postnatal overgrowth, mental retardation, and a characteristic facial appearance. He was admitted for treatment of multiple mandibular and maxillary cysts. Histopathological examination of the cyst tissue showed keratinized epithelium. Odontogenic keratocysts may have to be added to the typical features of this syndrome.

摘要

我们报告了一名患有智力发育迟缓-过度生长（辛普森-戈拉比-贝梅尔）综合征的10岁男孩。该患儿具有典型的临床特征，包括出生后过度生长、智力发育迟缓以及特征性面容。他因多发性下颌和上颌囊肿入院治疗。囊肿组织的组织病理学检查显示为角化上皮。牙源性角化囊肿可能需被纳入该综合征的典型特征之中。