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14 月龄患儿行联合硬化治疗后手术切除巨大颅外静脉畸形:术前评估和技术说明。

Combined sclerotherapy followed by surgical resection of a large extracranial venous malformation in a 14-month-old child: preoperative workup and technical note.

机构信息

Division of Neurosurgery, Faculty of Medicine, Geneva University Hospitals and University of Geneva, Rue Gabrielle-Perret-Gentil 4, 1205, Geneva, Switzerland.

Division of Diagnostic and Interventional Neuroradiology, Faculty of Medicine, Geneva University Hospitals and University of Geneva, Geneva, Switzerland.

出版信息

Childs Nerv Syst. 2023 Feb;39(2):527-533. doi: 10.1007/s00381-022-05643-z. Epub 2022 Aug 13.

Abstract

INTRODUCTION

Venous malformations affect around 2 per 10,000 newborn and are the most common type of congenital vascular malformation. They are always present at birth and are often misdiagnosed with hemangiomas. Accurate diagnosis and adequate targeted therapy through a multidisciplinary approach is advocated for a successful treatment, considering a combination of modalities in complex cases. We present here the workup and treatment of a venous malformation in a 14 month old child by combining a preoperative sclerotherapy with sodium tetradecyl sulfate (STS) followed by complete surgical excision respecting the calvarium.

CASE PRESENTATION

A large right extracranial fronto-parietal venous malformation and scalloping of the underlying calvarium, attached to the pericranium, surgically excised after preoperative sclerotherapy with STS in a 14-month-old child.

RESULTS

The patient had an uneventful postoperative course with complete resection of the lesion, satisfying cosmetic appearance and no complications. Histopathological examination confirmed a venous malformation.

CONCLUSION

We demonstrated the workup and the rationale of the combined sclerotherapy followed by surgical resection of a large growing extracranial venous malformation. Preoperative direct contrast injection and sclerotherapy allowed to rule out significative extracranial to intracranial venous inflow and reduce blood loss for the surgical procedure, respectively. Complete removal of the malformation minimized the impact on future growth of the calvarium.

摘要

简介

静脉畸形影响大约每 10000 名新生儿中的 2 名,是最常见的先天性血管畸形类型。它们在出生时就存在,并且经常被误诊为血管瘤。提倡通过多学科方法进行准确诊断和充分的靶向治疗,以获得成功的治疗效果,在复杂病例中考虑多种方法的组合。我们在此介绍了一名 14 个月大的儿童静脉畸形的检查和治疗方法,通过术前用十四烷基硫酸钠(STS)进行硬化治疗,然后在尊重颅骨的情况下完全切除。

病例介绍

一名 14 个月大的儿童,右侧颅外额顶静脉畸形,颅骨下有扇贝状凹陷,与颅骨膜相连,在术前用 STS 进行硬化治疗后,手术切除。

结果

患者术后无并发症,无并发症,病变完全切除,美容效果满意。组织病理学检查证实为静脉畸形。

结论

我们展示了大型生长性颅外静脉畸形的联合硬化治疗和手术切除的检查和治疗方法。术前直接对比注射和硬化治疗分别排除了重要的颅外到颅内静脉流入,并减少了手术中的失血量。畸形的完全切除最大限度地减少了对颅骨未来生长的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45d2/10006260/3c22806ad94c/381_2022_5643_Fig1_HTML.jpg

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