Tracz Jovanna A, Aldrete Aracelia, Scarcella Joshua, Inciong Jesus, Dilustro Joseph F, Guo Yifan
Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama.
School of Medicine, Eastern Virginia Medical School, Norfolk, Virginia.
J Neurosurg Case Lessons. 2025 Jun 2;9(22). doi: 10.3171/CASE24614.
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.
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.
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.
全层头皮坏死是减压性颅骨切除术(DC)后一种罕见的并发症,会使下方的硬脑膜和脑易受感染及进一步损伤。作者描述了一例2岁男性在急诊额颞顶DC术后出现头皮坏死并累及硬脑膜的病例,以及用于修复大面积头皮缺损和下方颅骨缺损的方法。还介绍了对头皮和颅骨联合缺损修复的系统评价结果。
在对坏死头皮进行清创后,进行了连续皮瓣推进以临时覆盖硬脑膜,并在硬脑膜上放置了真皮基质。使用组织扩张、聚醚醚酮植入物以及扩张皮瓣的旋转进行最终修复。在文献回顾中,有14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平方厘米。提出了一种针对复合性头皮和颅骨缺损的急性和长期管理及修复的算法。
DC术后小儿头皮缺损的长期修复需要基于患者因素的多学科方法,这些因素包括损伤病因、患者年龄、缺损大小以及头发生长潜力。https://thejns.org/doi/10.3171/CASE24614