Wider T M, Schwartz T H, Carmel P W, Wood-Smith D
Division of Plastic and Reconstructive Surgery, Columbia-Presbyterian Medical Center, New York, NY 10023, USA.
Ann Plast Surg. 1995 Apr;34(4):420-3. doi: 10.1097/00000637-199504000-00015.
Patients with Apert's syndrome typically exhibit craniosynostosis, exorbitism, midface hypoplasia, and symmetric syndactyly. There have also been occasional descriptions of the variable dysmorphology of the inner surface of the calvarium. We present a patient with Apert's syndrome who had an intracranial herniation of a portion of the frontal lobe through a ridge of ossified dura. The ridge and the gliotic cortical tissue were removed when the patient underwent repair of the hypertelorism at age six. Bone grafts for this repair were fashioned in part from the resected ridge. We believe this finding may be the result of a small dural tear that occurred during prior surgery.
患有阿佩尔综合征的患者通常表现为颅缝早闭、眼球突出、面中部发育不全和对称性并指(趾)畸形。也有偶尔关于颅骨内表面形态变异的描述。我们报告一名患有阿佩尔综合征的患者,其额叶的一部分通过骨化的硬脑膜嵴发生了颅内疝。该患者6岁接受眶距增宽修复手术时,切除了该嵴和胶质化的皮质组织。此次修复所用的骨移植部分取自切除的嵴。我们认为这一发现可能是先前手术中发生小的硬脑膜撕裂的结果。