al-Qattan M M, Thomson H G
Department of Surgery, Hospital for Sick Children, Toronto, Ontario, Canada.
Ann Plast Surg. 1994 May;32(5):550-2. doi: 10.1097/00000637-199405000-00022.
A rare case of a long-term survivor of Menkes' syndrome who was treated early and had excision of bilateral axillary skin excess is presented. Primary wound healing was observed and skin histology showed fragmentation of the elastic fibers. Two years after surgery, the scars appeared atrophic with evidence of early recurrence of the skin excess. The relationship between Menkes' syndrome and the other copper-related syndromes (X-linked cutis laxa, occipital horn syndrome, and Ehlers-Danlos syndrome type 1X) is also described.
本文报告了一例罕见的门克斯综合征长期存活者,该患者早期接受治疗并切除了双侧腋下多余皮肤。观察到伤口一期愈合,皮肤组织学显示弹性纤维断裂。术后两年,瘢痕出现萎缩,有皮肤多余早期复发的迹象。还描述了门克斯综合征与其他铜相关综合征(X连锁皮肤松弛症、枕角综合征和埃勒斯-当洛综合征1X型)之间的关系。