Park Eun Soo, Park Jun Ho, Shin Ho Seong, Nam Seung Min
*Department of Plastic and Reconstructive Surgery, College of Medicine, Soonchunhyang University, Bucheon †Department of Plastic and Reconstructive Surgery, College of Medicine, Soonchunhyang University, Gumi, Republic of Korea.
J Craniofac Surg. 2017 Nov;28(8):e788-e789. doi: 10.1097/SCS.0000000000004050.
Aplasia cutis congenita (ACC), also called cutis aplasia, is a rare congenital abnormality characterized by focal defect of the skin at birth, frequently involving the scalp, but may affect any region of the body. Approximately 80% of patients have the defect confined to the skin and generally less than 2 cm diameter, which can be managed conservatively with dressing alone. However, some patients present large cutaneous defects and aplasia of the underlying skull may also be present. The main complications of large defects include meningeal infection, bleeding, and thrombosis, which may be deadly. Some controversy remains in the literature regarding ACC treatment, with surgical and conservative treatment modalities having proponents and opponents.This article presents the first case of a newborn with full-thickness ACC lesion of the vertex healed by conservative treatment with application of acellular dermal matrix.
先天性皮肤发育不全(ACC),也称为皮肤发育不全,是一种罕见的先天性异常,其特征是出生时皮肤出现局灶性缺损,常累及头皮,但也可能影响身体的任何部位。大约80%的患者缺损仅限于皮肤,直径一般小于2厘米,仅通过换药即可保守治疗。然而,一些患者出现大面积皮肤缺损,还可能伴有颅骨发育不全。大面积缺损的主要并发症包括脑膜感染、出血和血栓形成,可能会致命。关于ACC的治疗,文献中仍存在一些争议,手术和保守治疗方式都有支持者和反对者。本文介绍了首例通过应用脱细胞真皮基质进行保守治疗治愈的新生儿头顶全层ACC病变病例。