儿童患者颅骨减压切除术后的头皮坏死:说明性病例。

Jovanna A Tracz, Aracelia Aldrete, Joshua Scarcella, Jesus Inciong, Joseph F Dilustro, Yifan Guo
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引用次数: 0

摘要

背景:全层头皮坏死是颅骨减压切除术(DC)后罕见的并发症,使底层硬脑膜和大脑易受感染和进一步损伤。作者描述了一名2岁男性在急诊额颞顶DC后出现头皮坏死延伸至硬脑膜的病例,此外还使用了重建大面积头皮缺损和潜在颅骨缺损的方法。结果系统回顾重建合并头皮和颅骨缺损也提出。观察:坏死头皮清创后,连续皮瓣推进进行临时硬脑膜覆盖,在硬脑膜上放置真皮基质。使用组织扩张、聚醚醚酮植入物和扩张皮瓣旋转进行最终重建。在文献回顾中,14例病例符合纳入标准。患者平均年龄为9个月,头皮缺损平均面积为61 cm2。提出了一种头皮和颅骨复合缺损的急性和长期治疗和重建算法。经验:儿童头皮缺损DC后的长期重建需要基于患者因素的多学科方法,包括损伤的病因、患者的年龄、缺损的大小和头发再生的潜力。https://thejns.org/doi/10.3171/CASE24614。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Scalp necrosis following decompressive craniectomy in pediatric patient populations: illustrative case.

Background: Full-thickness scalp necrosis is a rare complication following decompressive craniectomy (DC), leaving the underlying dura mater and brain vulnerable to infection and further injury. The authors describe a case of scalp necrosis extending down to the dura in a 2-year-old male following emergency frontotemporoparietal DC, in addition to the method used for reconstruction of both the large scalp defect and the underlying skull defect. The results of a systematic review of reconstruction of combined scalp and calvarial defects are also presented.

Observations: Following debridement of the necrotic scalp, serial flap advancements were performed for temporary dural coverage, with a dermal matrix placed over the dura. Definitive reconstruction was performed using tissue expansion, a polyetheretherketone implant, and rotation of the expanded flap. In a review of the literature, 14 cases met the inclusion criteria. The mean patient age was 9 months, and the mean size of the scalp defect was 61 cm2. An algorithm for acute and long-term management and reconstruction of composite scalp and calvarial defects is proposed.

Lessons: Long-term reconstruction of pediatric scalp defects following DC requires a multidisciplinary approach based on patient factors including etiology of injury, patient age, size of the defect, and potential for hair regrowth. https://thejns.org/doi/10.3171/CASE24614.

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