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[多发性痣样基底细胞癌综合征]

[Syndrome of multiple nevoid basal cell carcinoma].

作者信息

Morais Pérez D, Santos Martí J M, Fernández Gómez J, Bernat Gilli A, Ayerbe Torrero V

机构信息

Servicio de O.R.L. Hospital del Insalud de Barbastro, Huesca.

出版信息

An Otorrinolaringol Ibero Am. 1991;18(3):293-300.

PMID:1897709
Abstract

The paramount features of the multiple nevoid basal Carcinoma, the so-called Gorlin's syndrome, are the presence of multiple maxillary cysts (odontogenic keratocysts), several nevoid basal cells carcinomata and some skeletal anomalies. Since its first description, due to Jarish (1894), at least about 250 cases have been published. The odontogenic keratocysts present themselves with ENT symptoms, specially when arising on the upper maxillary bone or on the homonymous sinus. Owing to this reason, the AA. of the paper, recall the clinic aspects of the condition.

摘要

多发性痣样基底细胞癌,即所谓的戈林综合征,其主要特征是存在多个上颌囊肿(牙源性角化囊肿)、多个痣样基底细胞癌以及一些骨骼异常。自1894年贾里什首次描述该病以来,至少已发表了约250例病例。牙源性角化囊肿会引发耳鼻喉症状,特别是当它出现在上颌骨或同名鼻窦时。出于这个原因,本文作者回顾了该病症的临床方面。

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