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一名患有Klippel-Feil综合征的成年患者枕部皮样窦合并感染性畸胎瘤:罕见病例报告及文献综述

Occipital dermal sinus associated with infectious teratoma in an adult patient affected by Klippel-Feil syndrome: Rare case report and literature review.

作者信息

Nery Breno, Durand Victoria Rodrigues, Rabello Rafael De Almeida, De Oliveira Anna Carolyne Mendes, Quaggio Eduardo, Ortega Manoela Marques, Camporezi Bruno, Segundo José Alencar De Sousa

机构信息

Department of Neurosurgery, Beneficência Portuguesa, Ribeirão Preto, Brazil.

出版信息

Surg Neurol Int. 2024 Mar 22;15:94. doi: 10.25259/SNI_1024_2023. eCollection 2024.

Abstract

BACKGROUND

The Klippel-Feil syndrome (KFS) is a rare congenital anomaly characterized by the fusion of cervical vertebrae, which may be associated with other malformations, such as dermoid tumors and teratoma. Some theories explain the embryology of these associations. Another condition that may be present is the dermal sinus (DS), communication between intracranial tumors and the subcutaneous tissue, and predisposing infections. This case report aims to describe an association between these three pathologies as well as correlate them from the literature. This report was based on medical records retrospectively reviewed associated with the systematic bibliographical consultation using indexed databases based on inclusion and exclusion methods.

CASE DESCRIPTION

An adult male patient, 24 years old, was admitted to our service, presenting fever and meningeal irritation as initial symptoms. In the patient's clinical history, he was diagnosed with an occipital DS in his childhood, which was previously instructed to be operated on by another neurosurgical team, but the patient chose not to perform the procedure. The magnetic resonance imaging investigation showed a DS associated with a cerebellar infected mass with 2 cm on its main diameter. The patient was treated with preoperative antibiotic therapy and underwent gross total surgical resection of the tumor as well as DS correction, confirmed in the histopathological examination as a teratoma. After surgery, further computed tomography scan analysis showed the presence of cervical vertebrae fusion, compatible with KFS diagnosis.

CONCLUSION

The association between KFS, cerebellar teratoma, and DS has not yet been described in the literature, with only the association of the first two being extremely rare.

摘要

背景

克-费综合征(KFS)是一种罕见的先天性异常,其特征为颈椎融合,可能与其他畸形相关,如皮样肿瘤和畸胎瘤。一些理论解释了这些关联的胚胎学。另一种可能存在的情况是皮样窦(DS),即颅内肿瘤与皮下组织之间的连通,并易引发感染。本病例报告旨在描述这三种病理情况之间的关联,并将它们与文献进行对比。本报告基于回顾性审查的病历,并结合使用基于纳入和排除方法的索引数据库进行系统的文献检索。

病例描述

一名24岁成年男性患者入住我院,最初症状为发热和脑膜刺激征。在患者的临床病史中,他童年时被诊断出患有枕部皮样窦,此前另一个神经外科团队曾建议进行手术,但患者选择不进行该手术。磁共振成像检查显示皮样窦与一个小脑感染性肿块相关,肿块最大直径为2厘米。患者接受了术前抗生素治疗,并接受了肿瘤的全切除以及皮样窦矫正手术, 组织病理学检查证实为畸胎瘤。术后,进一步的计算机断层扫描分析显示存在颈椎融合,符合克-费综合征的诊断。

结论

克-费综合征、小脑畸胎瘤和皮样窦之间的关联在文献中尚未见报道,仅前两者的关联极为罕见。

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