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首页> 外文期刊>Journal of Research in Dental Sciences >Basal cell nevus syndrome (Gorlin-Goltz) : A Case Report
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Basal cell nevus syndrome (Gorlin-Goltz) : A Case Report

机译:基底细胞痣综合征(Gorlin-Goltz):一例报告

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Abstract: ??? Backround: Basal cell nevus syndrome (BCNS) is an autosomal dominant inherited condition. ? The syndrome presents with multiple jaw cysts (more often,OKC), skeletal abnormalities ,ectopic intracranial calcification , multiple basal cell carcinomas of the skin . The prevalence of Gorlin syndrome is estimated to be about 1/60000 to 1/120000 . This syndrome if often distinguished in third decade of life.In this article a rare case of Basal cell nevus syndrome is reported. ??? Case presentation : The case was a 23 year- old male patient with the chief complaint of exiting pus from the left side of his mandible ( Buccal of first molar) who was referred to Islamic Azad University (Dental Branch) Radiology Dept. In radiographic assessment (panoramic radiography) multiple cystic lesions and thus impacted teeth in maxilla were seen . In histopathological view, epithelium of odontogenic cyst , keratin debries and Palisaded basal cells were seen in both jaws. The definitive diagnosis was multiple odontogenic keratocysts. Treatment was done first by marsupialization , enuclation and curettage. In three months follow up, recurrance wasnot seen. ??? Conclusion: Early diagnosis of Basal Cell Nevus Syndrome (BCNS) by dentists or dental specialists play an important role in patients' prognosis.
机译:摘要:背景:基底细胞痣综合征(BCNS)是常染色体显性遗传病。 ?该综合征表现为多发性颌骨囊肿(OKC),骨骼异常,异位颅内钙化,皮肤多发基底细胞癌。据估计,戈林综合症的患病率约为1/60000至1/120000。如果经常在生命的第三个十年中区分出这种综合症。本文报道了罕见的基底细胞痣综合症。 ???病例介绍:该病例为一名23岁的男性患者,主要主诉是从下颌骨左侧(第一磨牙颊侧)流出脓液,该患者转诊至伊斯兰阿扎德大学(牙科分校)放射科。 (全景X线摄影)可见多个囊性病变,因此上颌牙齿受到影响。从组织病理学的角度来看,在两个颌骨中均可见牙源性囊肿,角蛋白碎片和呈鳞状的基底细胞的上皮。明确的诊断是多个牙源性角化囊肿。首先通过有袋化,结石和刮宫术进行治疗。在三个月的随访中,未见复发。 ???结论:牙医或牙科专家对基底细胞痣综合征(BCNS)的早期诊断在患者的预后中起着重要作用。

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