Moscona R, Berger J, Govrin J
Department of Plastic Surgery, Rambam Medical Center, Haifa, Israel.
Ann Plast Surg. 1991 Feb;26(2):178-82. doi: 10.1097/00000637-199102000-00012.
Nine patients with aplasia cutis congenita were treated in our department during the past 30 years. Of these, 1 patient died due to uncontrolled hemorrhage and 1 patient was operated on by using a pericranial flap to cover a 7 x 5-cm scalp defect with large bony involvement. After 5 years of follow-up, the skull defect closed completely by normal bone that can be palpated on examination and seen on radiographs.
在过去30年里，我们科室共治疗了9例先天性皮肤发育不全患者。其中，1例患者因出血无法控制而死亡，1例患者接受了颅骨膜瓣手术，以覆盖一个7×5厘米、伴有大面积骨质受累的头皮缺损。经过5年的随访，颅骨缺损已完全由正常骨质闭合，在检查时可触及，X线片上也可见到。
