Suppr超能文献

伴有骨质溶解和经颅骨疝出的巨大出血性及脓肿性儿童高级别胶质瘤:一种独特表现及文献综述

Giant hemorrhagic and abscessed pediatric high-grade glioma with osteolysis and transcalvarial herniation: A unique presentation and literature review.

作者信息

Borni Mehdi, Taallah Marouen, Kammoun Brahim, Daoud Hatem, Belmabrouk Houda, Boudawara Mohamed Zaher

机构信息

Department of Neurosurgery, Habib Bourguiba University Hospital, Sfax, Tunisia.

Department of Neurosurgery, Habib Bourguiba University Hospital, Sfax, Tunisia.

出版信息

Int J Surg Case Rep. 2025 Aug 7;135:111748. doi: 10.1016/j.ijscr.2025.111748.

Abstract

INTRODUCTION

High-grade gliomas (HGGs) in very young children are rare, with intratumoral abscess formation being exceptionally uncommon and primarily reported in adults. We present a unique pediatric case with this rare complication.

CASE REPORT

A 5-month-old female infant, born after a complicated pregnancy, presented with rapidly progressive intracranial pressure. Imaging revealed a large, hemorrhagic, left parieto-occipital lesion with osteolysis and subsequent transcalvarial herniation. Intraoperatively, a culture-negative abscess was found within the tumor. Initial biopsy suggested a low-grade glioma, but final histopathology confirmed a high-grade glioma.

DISCUSSION

The combination of a giant, abscessed, and osteolytic HGG leading to transcalvarial herniation in a young infant is unprecedented. Intratumoral abscesses in pediatric HGGs are not previously documented, making this case a significant addition to the literature. The sterile abscess may be linked to tumor necrosis or the patient's perinatal history. This atypical presentation underscores the diverse nature of pediatric HGGs.

CONCLUSION

This first reported case of a giant, hemorrhagic, osteolytic, and abscessed pediatric HGG with transcalvarial herniation highlights an exceptionally rare and aggressive presentation in a very young infant. It emphasizes the need for considering unusual features in pediatric brain tumors and warrants further investigation into the pathogenesis and management of such complex lesions.

摘要

引言

极低龄儿童的高级别胶质瘤(HGGs)较为罕见,瘤内形成脓肿的情况尤为罕见,主要见于成人。我们报告了一例具有这种罕见并发症的独特儿科病例。

病例报告

一名5个月大的女婴,在经历复杂妊娠后出生,出现颅内压迅速升高。影像学检查显示左侧顶枕叶有一个巨大的出血性病变,伴有骨质溶解及随后的颅骨外疝形成。术中,在肿瘤内发现一个培养结果为阴性的脓肿。初步活检提示为低级别胶质瘤,但最终组织病理学确诊为高级别胶质瘤。

讨论

巨大、有脓肿形成且骨质溶解的高级别胶质瘤导致幼婴颅骨外疝,这种情况前所未见。儿科高级别胶质瘤中的瘤内脓肿此前未见报道,因此该病例为文献增添了重要内容。无菌性脓肿可能与肿瘤坏死或患者围产期病史有关。这种非典型表现突显了儿科高级别胶质瘤的多样性。

结论

首例报道的患有巨大、出血、骨质溶解且有脓肿形成并伴有颅骨外疝的儿科高级别胶质瘤病例,突显了在极低龄幼婴中一种极其罕见且侵袭性强的表现形式。它强调了在儿科脑肿瘤中考虑不寻常特征的必要性,并值得进一步研究此类复杂病变的发病机制和治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad8/12410355/824ff5ef8a28/gr1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验