Harvey Georgina, Solanki Nicholas S, Anderson Peter J, Carney Bernard, Snell Broughton J
From the *Department of Plastic and Reconstructive Surgery and †The Australian Craniofacial Unit, Women's and Children's Hospital, North Adelaide, SA, Australia.
J Craniofac Surg. 2012 Nov;23(6):1662-4. doi: 10.1097/SCS.0b013e31826542de.
Aplasia cutis congenita (ACC) is a rare condition commonly affecting the scalp in which there is a focal deficiency of cutaneous tissues of varying severity ranging from an absence of skin through to full thickness defects involving deeper elements such as bone and dura. Lesions of the scalp can be associated with complications including infection, hemorrhage, thrombosis, and seizures. Opinions in the current literature regarding management of this condition are varied with both conservative and surgical management advocated. Conservative treatment consists of regular wound dressings and systemic antibiotics, while surgical management commonly involves skin grafting and local flaps.
A retrospective case review was performed to audit the outcomes of patients with ACC of the scalp managed at the Women's and Children's Hospital (WCH) in Adelaide, Australia from 2002 to 2012. Cases were identified from admission coding diagnoses and data was retrieved from patient case notes.
Seventeen cases of ACC were identified. The most common location involved was the scalp vertex. Thirteen patients were managed conservatively and 4 had primary surgical intervention. Of the cases that were managed with primary surgery, 2 had complications. None of the conservatively managed patients had complications in the acute setting.
At the WCH, we advocate adopting a conservative approach to management of ACC of the scalp. Defects can be successfully managed with a combination of regular dressings and systemic antibiotics. Regular wound monitoring is essential to detect any complications early to instigate appropriate treatment and determine the need for emergency surgical management.
先天性皮肤发育不全(ACC)是一种罕见病症,通常累及头皮,表现为不同严重程度的皮肤组织局灶性缺损,从无皮肤到全层缺损,累及骨骼和硬脑膜等深层结构。头皮病变可能伴有感染、出血、血栓形成和癫痫发作等并发症。目前文献中对于该病症的治疗意见不一,既有保守治疗也有手术治疗的主张。保守治疗包括定期伤口换药和全身使用抗生素,而手术治疗通常涉及皮肤移植和局部皮瓣转移。
进行一项回顾性病例分析,以审核2002年至2012年在澳大利亚阿德莱德妇女儿童医院(WCH)接受治疗的头皮ACC患者的治疗结果。通过入院编码诊断确定病例,并从患者病历中检索数据。
共确定17例ACC病例。最常累及的部位是头皮顶部。13例患者接受保守治疗,4例接受一期手术干预。在接受一期手术治疗的病例中,2例出现并发症。在急性阶段,保守治疗的患者均未出现并发症。
在WCH,我们主张采用保守方法治疗头皮ACC。通过定期换药和全身使用抗生素可成功处理缺损。定期伤口监测对于早期发现任何并发症、启动适当治疗以及确定是否需要紧急手术治疗至关重要。