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颅骨肉样瘤病:系统评价。

Sarcoidosis of the Skull: A Systematic Review.

机构信息

Section of Neurosurgery, Hospital CMQ Premier, Puerto Vallarta, Jalisco, Mexico.

Section of Internal Medicine, Hospital CMQ Premier, Puerto Vallarta, Jalisco, Mexico.

出版信息

World Neurosurg. 2020 Jul;139:387-394. doi: 10.1016/j.wneu.2020.04.114. Epub 2020 Apr 24.

Abstract

BACKGROUND

Lesions of the skull make up a small but important part of neurosurgical practice. Several systemic disorders may involve the cranial vault including neoplastic and non-neoplastic conditions. Sarcoidosis of the skull is a little-known cause of calvarial involvement that has been rarely reported in the literature. The available information about skull sarcoidosis (SS) is sparse and is not well described; for this reason, we consider that a detailed description of this uncommon condition is necessary.

METHODS

An illustrative case of SS is presented; in addition, a PubMed and Scopus search adhering to Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines was performed to include studies reporting patients with SS. Different information was analyzed in these cases to describe the characteristics of this condition. Also, different sources of literature were analyzed to complete the description of this clinical entity.

RESULTS

The search yielded 22 cases of patients with SS showing a variety of clinical manifestations. All studies were case reports. Most patients diagnosed with SS had no previous history of systemic sarcoidosis. Different characteristics of SS are analyzed and described in this paper.

CONCLUSIONS

The information collected from this review shows that SS is a rare condition that frequently is observed in patients without previous diagnosis of sarcoidosis. SS may manifest in different ways, and even may be found incidentally in some patients. The diagnosis of SS should be considered when multiple lytic skull lesions are observed, especially in cases of patients without a previous history of malignancy.

摘要

背景

颅骨病变构成神经外科实践中的一小部分,但却非常重要。几种系统性疾病可能涉及颅腔,包括肿瘤性和非肿瘤性疾病。颅骨结节病是颅骨受累的一种鲜为人知的原因,在文献中很少有报道。关于颅骨结节病(SS)的可用信息很少,并且描述得不够详细;因此,我们认为有必要详细描述这种罕见的疾病。

方法

介绍了一例 SS 病例;此外,还按照系统评价和荟萃分析的首选报告项目指南,对 PubMed 和 Scopus 进行了搜索,以纳入报告 SS 患者的研究。对这些病例中的不同信息进行了分析,以描述该病症的特征。此外,还分析了不同的文献来源,以完成对该临床实体的描述。

结果

搜索结果显示有 22 例 SS 患者的病例,表现出多种临床表现。所有研究均为病例报告。大多数被诊断为 SS 的患者以前没有系统性结节病的病史。本文分析并描述了 SS 的不同特征。

结论

从本次综述中收集到的信息表明,SS 是一种罕见的疾病,经常发生在以前没有结节病诊断的患者中。SS 可能以不同的方式表现出来,甚至在一些患者中也可能偶然发现。当观察到多个溶骨性颅骨病变时,尤其是在没有先前恶性肿瘤病史的患者中,应考虑 SS 的诊断。

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