Leboucq N, Montoya y Mártínez P, Montoya-Vigo F, Catan P
Department of Neuroradiology, Centre Hospitalier Universitaire, Montpellier, France.
Neuroradiology. 1994 Aug;36(6):480-2. doi: 10.1007/BF00593689.
Localised agenesis of the scalp is the most frequent pattern in aplasia cutis congenita (ACC), a congenital absence of the skin and occasionally of deeper layers. Several clinical groups are characterised by the location and pattern of skin defects, associated malformations and the mode of inheritance. Death occurs in 20% of cases, secondary to the associated anomalies, to infections or to haemorrhage from ulceration of the sagittal sinus when there is also a defect of the underlying skull. In this latter case, we close the defect by two rotational scalp flaps (Orticochea technique) at birth. A three-dimensional CT study is useful for showing the extent of the skull defect and the deformity of the craniofacial complex and the changes in the bone after treatment.
局限性头皮发育不全是先天性皮肤发育不全(ACC)最常见的表现形式,ACC是一种先天性皮肤缺失,偶尔也会累及更深层组织。几个临床组的特征在于皮肤缺损的位置和模式、相关畸形以及遗传方式。20%的病例会因相关异常、感染或矢状窦溃疡出血(当颅骨也存在缺损时)而死亡。在后一种情况下,我们在出生时通过两个旋转头皮瓣(奥尔蒂乔亚技术)闭合缺损。三维CT研究有助于显示颅骨缺损的范围、颅面复合体的畸形以及治疗后骨骼的变化。