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Gorlins syndrome or nevoid basal cell carcinoma syndrome.

机译:戈林综合症或无基底细胞癌综合症。

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摘要

Gorlin's syndrome is a condition inherited in an autosomal dominant fashion. It involves many organs, but principally affects the skin, skeleton, and endocrine and nervous systems. The most common features are multiple nervi and basal cell carcinomas of the skin, benign jaw cysts, dyskeratotic pits in the palms and soles, rib and vertebral abnormalities, brachymetacarpalism, and calcification of the falx cerebri. In 14 patients, 4 of whom belonged to one family, the age at the time of diagnosis ranged from 11 to 63 years. Ten patients are alive, but five are severely disfigured by carcinomas. Two patients died of complications resulting from uncontrolled tumours, and two died of other cancers. New skin tumours constantly develop; small ones can be excised, but large ones require extensive surgery with or without radiotherapy.
机译:高林氏综合征是一种以常染色体显性遗传的疾病。它涉及许多器官,但主要影响皮肤,骨骼以及内分泌和神经系统。最常见的特征是皮肤多发性神经和基底细胞癌,良性下颌囊肿,手掌和脚底的角化不全坑,肋骨和椎骨异常,近腕掌骨症和镰状小脑钙化。在14位患者中,其中4位属于一个家庭,诊断时的年龄为11至63岁。十名患者还活着,但五名因癌症而严重毁容。两名患者死于肿瘤不受控制的并发症,两名死于其他癌症。新的皮肤肿瘤不断发展;小型手术可以切除,但是大型手术需要接受或不接受放射治疗的广泛手术。

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