Gorlin - Goltz综合征1例报告

Mahesh Chander , Madan Mishra , Amit Gaur , Tasveer Fatima , Shubhamoy Mondal , Shishir Dhar
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引用次数: 0

摘要

在印度报告的病例并不多,因此我们在此报告一例罕见的Gorlin - Goltz综合征(GGS),特别是在没有任何皮肤病变的年轻患者中。一名21岁男性向我科报告,右下颌后下区域肿胀2年。彻底的口外和口内检查以及骨断层扫描(OPG), CT扫描(颅骨)和胸片有助于正确诊断病情。未见基底细胞痣、掌、足底凹陷或角化病等皮肤病变。所有颌骨囊性病变均行手术去核及卡诺氏液化学烧灼。至今未见复发迹象。我们的病例强调了认识这种罕见综合征的重要性,特别是在没有任何皮肤病变的年轻患者中,因为早期确认疾病可以预防复发,并提高现有疾病的存活率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gorlin Goltz syndrome: A case report

Not many cases have been reported in India, and hence we report here a rare case of Gorlin Goltz syndrome (GGS) especially in young patients without any skin lesions. A 21 year old male reported to our department, with swelling in the lower posterior region of the right side of jaw since last 2 years. Thorough extraoral and intraoral examinations along with orthopantomogram (OPG), CT scan (skull) and chest radiograph helped in proper diagnosis of the condition. No skin lesion in the form of basal cell nevus, palmar or plantar pits, or keratosis were present. All the cystic lesions of the jaws were enucleated surgically and chemical cauterization done by Carnoy's solution. No sign of recurrence observed still date. Our case highlights the importance of the awareness of this rare syndrome, especially in young patients without any skin lesions because early verification of the disease prevent recurrence and better survival rates from the existent disease.

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