...
首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Dilemmas and challenges in the management of a neonate with Adams-Oliver syndrome with infected giant aplasia cutis lesion and exsanguination: A case-based update
【24h】

Dilemmas and challenges in the management of a neonate with Adams-Oliver syndrome with infected giant aplasia cutis lesion and exsanguination: A case-based update

机译:患有巨人发育不全病变和放血的Adams-Oliver综合征新生儿的处理中的困境和挑战:基于案例的更新

获取原文
获取原文并翻译 | 示例

摘要

Background: Aplasia cutis is a rare developmental anomaly usually involving the calvarium, associated with a variable extent of defective formation of the scalp. Adams-Oliver syndrome is a condition mainly characterized by the congenital absence of skin, known as "aplasia cutis" which is usually limited to the vertex scalp and transverse limb defects. Case report: A 17-day-old term female neonate was referred to us with an infected scalp lesion of the vertex. The lesion which is about 10 × 9 cm had signs of infection with necrotic eschar. We started the neonate on systemic parenteral antibiotics with local dressings. On day 3 of conservative management, the neonate had exsanguination due to bleeding from the midline with severe hemodynamic compromise requiring cardiopulmonary resuscitation. After controlling the bleeding with local tamponade and resuscitating the child, she was taken for early surgery. Debridement and bipedicled rotation flap of the scalp to cover the raw area was performed. On day 18, the flap started showing signs of necrosis. The neonate was taken up for debridement, and subsequently, maternal allograft of split-thickness skin was placed as a temporary wound cover. Meanwhile, the wound showed progressive epithelialization. At 1 year, the patient continued to have a non-healing area, which was later successfully covered with a split-thickness skin graft. We plan to revaluate the need for cranioplasty at around 3-4 years of age. Discussion: We discuss the dilemmas and challenges involved in the successful management of a neonate with Adams-Oliver syndrome with infected aplasia cutis and an episode of life-threatening exsanguination. Conclusion: Aplasia cutis is a rare developmental anomaly usually involving the calvarium, associated with defective formation of the scalp to a varying extent and severity, requiring various timely strategies.
机译:背景:皮肤发育不良是一种罕见的发育异常,通常涉及颅骨,与头皮形成缺陷的程度不同。亚当斯-奥利弗综合症是一种主要以先天性皮肤缺乏为特征的疾病,称为“皮膜缺乏症”,通常仅限于头皮和横肢缺损。病例报告:一名17天大的女新生儿被转介给我们,感染了头皮的顶点病变。病变约10×9 cm,有坏死性焦char感染迹象。我们开始使用局部敷料对全身性肠胃外抗生素进行新生儿治疗。保守治疗的第3天,新生儿因中线出血而严重放血,需要进行心肺复苏,导致放血。在用局部填塞物控制了出血并恢复了孩子的生命之后,她被送去进行早期手术。进行清创术和头皮的双蒂旋转皮瓣覆盖原始区域。在第18天,皮瓣开始出现坏死的迹象。采集新生儿进行清创术,随后将同种异体皮肤的母亲同种异体移植物作为临时伤口覆盖物。同时,伤口表现出进行性上皮化。在1年时,患者继续处于无法愈合的区域,随后成功地用了裂厚的皮肤移植物覆盖了该区域。我们计划在3-4岁左右重新评估颅骨成形术的必要性。讨论:我们讨论了成功治疗患有亚当斯-奥利夫综合征的皮肤角质不全症和危及生命的放血事件的新生儿成功治疗所涉及的困境和挑战。结论:皮肤发育不良是一种罕见的发育异常,通常涉及颅骨,在不同程度上和严重程度与头皮缺陷形成相关,需要采取各种及时的策略。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号