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Delayed Diagnosis of Gorlin-Goltz Syndrome: The Importance of the Multidisciplinary Approach

机译:荷兰林 - Goltz综合征的延迟诊断:多学科方法的重要性

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Gorlin-Goltz syndrome (GGS), also known as nevoid basal cell carcinoma syndrome, is an autosomal dominant inherited disorder with high penetrance and variable expressivity. The classic triad originally described by Gorlin and Goltz in 1960 is composed of multiple nevoid basal cell carcinomas (NBCCs), odontogenic keratocysts (OKCs) in the jaws and bifid ribs. in 1977, this triad was modified by Rayner et al, and to GGS diagnosis, the OKCs had to appear in combination with calcification of the cerebellar falx or pal mar and plantar pits. It may occur that although GGS syndrome is a well-known condition, only the specific symptom could he observed by different specialists. Therefore, the patient cannot be placed in an always complex clinical panel. The authors introduce an example in this report. In the present case, the patient had NBCCs, OKCs, and probably other signs of GGS since 1998, and has been treated for this conditions separated, without a diagnosis of a syndromic condition. A 54-year-old white woman was referred to the oral medicine service due to cyst located in the right mandibular body. She had history of skin cancer and undergone surgeries and radiotherapies for the lesions treatment, scars on the skin face due to the lesions removed, and a new ulcerated lesion on the back of was diagnosed. In addition, the patient presented frontal and parietal bossing leading to increased cranial circumference, hypertelorism, strabismus, broad base, and mandibular prognathism. To the image 9w?examination, skull radiography revealed calcification of the falx cerebri; on chest X-ray bifid rib was observed and spine radiography showed vertebral osteophytes. Panoramic radiograph showed a well-defined bilocular radiolucent image located in posterior and anterior mandibular region. The whole elements induced us to investigate the patient's past medical history, which revealed that since 1998 had the diagnosis of NBCC and OKC. A multidisciplinary approach becomes necessary for the diagnosis and follow-up of patients with GGS, considering the complexity of the clinical manifestations. Therefore, it is of primary importance for dental surgeons and dermatologists to know the signs and symptoms of GGS to perform early diagnosis and to avoid progression of the oral cysts or metastasis of the skin lesions.
机译:Gorlin-Goltz综合征(GGS),也称为Nevoid基础细胞癌综合征,是一种常染色体显性遗传性障碍,具有高的渗透和可变性的敏感性。 1960年最初由Gorlin和Goltz描述的经典三合会由钳口和双歧肋的多态基底细胞癌(NBCC),牙突菌(OKC)组成。 1977年,该三合会由Rayner等人修改,并且GGS诊断,OKC必须与Cerebellar Falx或Pal和Plantar Pits的钙化结合使用。可能会发生,尽管GGS综合征是一个众所周知的病症,但他只能观察到不同专家的特定症状。因此,患者不能放置在始终复杂的临床面板中。作者在本报告中介绍了一个例子。在目前的情况下,自1998年以来,患者患有NBCC,OKC,以及GGS的其他迹象,并且已被对该条件进行治疗,而不会诊断综合征病症。由于位于右侧下颌体的囊肿,一名54岁的白人女性被称为口腔医学服务。她患有皮肤癌的历史,并经过手术和放射治疗的放射治疗,由于除去病变,皮肤面上的疤痕,并且诊断出后面的新溃疡病变。此外,患者展示了前部和顶视讲座,导致颅周,高度兴奋,斜视,宽底座和下颌预后性增加。到图像9W?&检查,颅骨放射线照相揭示了Falx Cerebri的钙化;在胸部X射线双歧肋观察并脊柱射线照相显示椎骨骨赘。全景Xcextopropl显示出位于后颌骨区域中的明确定义的双目无辐射图像。整个元素诱导我们调查患者过去的病史,从而揭示了1998年以来的诊断NBCC和OKC。考虑到临床表现的复杂性,M多学科方法是诊断和后续患者的诊断和随访。因此,对于牙科外科医生和皮肤科医生来说,了解GGS的迹象和症状,并且避免皮肤病患者口腔囊肿或转移的进展是初步的重要性。

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