Wehrens Kim M, De Jongh Frank, Ter Laak M P, Cornips E M, Van der Hulst Rrwj
Plastic Surgery, Haaglanden Medisch Centrum, The Hague, NLD.
Neurosurgery, Maastricht University Medical Center, Maastricht, NLD.
Cureus. 2020 Feb 19;12(2):e7047. doi: 10.7759/cureus.7047.
Adams-Oliver syndrome (AOS) is a rare congenital disorder characterised by a wide variety of clinical expression ranging from the occurrence of aplasia cutis congenita (ACC), transverse limb defects, and cutis marmorata telangiectica to extensive lethal anomalies. In this article, we present the conservative and surgical management of a male newborn infant diagnosed with AOS. Surgical treatment included wound management, the removal of protruding brain, and treatment of cerebrospinal fluid (CSF) leakage. After spontaneous reepithelization of the wounds, conservative treatment was chosen instead of reconstruction with an occipital flap; this was continued until the total healing of the dermal defect after eight months, during which the patient was continuously treated with antibiotics. At 17 months, the child was in good physical condition with a three-month development delay in comparison with infants of his age and no evidence of neurological deficit.
亚当斯-奥利弗综合征(AOS)是一种罕见的先天性疾病,其临床表型多样,从先天性皮肤发育不全(ACC)、肢体横断缺损、大理石样皮肤血管扩张到广泛的致死性畸形。在本文中,我们介绍了一名被诊断为AOS的男婴的保守治疗和手术治疗情况。手术治疗包括伤口处理、突出脑组织切除以及脑脊液(CSF)漏治疗。伤口自发重新上皮化后,选择了保守治疗而非枕叶皮瓣重建;这种治疗持续到八个月后皮肤缺损完全愈合,在此期间患者持续接受抗生素治疗。17个月时,该患儿身体状况良好,但与同龄婴儿相比有三个月的发育延迟,且无神经功能缺损迹象。