David D J, Moore M H, Cooter R D, Chow S K
South Australian Cranio-Facial Unit, Adelaide Children's Hospital.
Plast Reconstr Surg. 1989 Mar;83(3):520-7. doi: 10.1097/00006534-198903000-00022.
The clinical, radiologic, and operative examination of two patients with the Tessier number 9 cleft has allowed the first complete description of this, the rarest of the rare craniofacial clefts. Soft-tissue disruption extends from the lateral third of the upper eyelid through a distorted lateral end of the eyebrow to the temporal scalp, with an associated hairline indicator. The skeletal disturbance similarly radiates superolaterally from the superolateral orbital rim across the greater wing of the splenoid to the upper squamous temporal. The three-dimensional extent of the bony disruption is associated with distortion of the cranial base and calvaria above.
对两名患有第9号泰西埃裂的患者进行的临床、放射学和手术检查,首次完整描述了这种极为罕见的颅面裂。软组织破坏从右上眼睑外侧三分之一处延伸,穿过扭曲的眉外侧端至颞部头皮,并伴有发际线异常。骨骼紊乱同样从眶上外侧缘向外上辐射,穿过蝶骨大翼至上颞鳞状部。骨破坏的三维范围与上方颅底和颅骨的变形有关。