Chuman Hideki, Trobe Jonathan D, Petty Elizabeth M, Schwarze Ulrike, Pepin Melanie, Byers Peter H, Deveikis John P
Department of Ophthalmology, University of Michigan Medical Center, Ann Arbor, USA.
J Neuroophthalmol. 2002 Jun;22(2):75-81. doi: 10.1097/00041327-200206000-00002.
Two unrelated adults with Ehlers-Danlos syndrome type IV developed acute unilateral ophthalmoplegia and ipsilateral headache as a consequence of spontaneous (nontraumatic) direct carotid-cavernous fistulas. Because the interventional radiologist suspected the diagnosis of Ehlers-Danlos syndrome type IV, the carotid-cavernous fistulas were closed via the venous rather than the more standard arterial route in an attempt to avoid arterial dissection or rupture. In any patient presenting with a spontaneous direct carotid-cavernous fistula, family history and clinical examination should be targeted toward a diagnosis of Ehlers-Danlos syndrome type IV because of risks attendant to angiography and repair of the fistula. For these patients, ancillary medical care must be approached cautiously to avoid hollow viscus rupture. Molecular tests can be used to confirm the diagnosis and provide family members with accurate genetic counseling and predictive genetic testing.
两名患有IV型埃勒斯-当洛综合征(Ehlers-Danlos syndrome type IV)的非亲属成年人因自发性(非创伤性)直接颈动脉海绵窦瘘而出现急性单侧眼肌麻痹和同侧头痛。由于介入放射科医生怀疑为IV型埃勒斯-当洛综合征,为避免动脉夹层或破裂,通过静脉而非更标准的动脉途径封闭了颈动脉海绵窦瘘。对于任何出现自发性直接颈动脉海绵窦瘘的患者,由于血管造影和瘘管修复存在风险,家族史和临床检查应针对IV型埃勒斯-当洛综合征的诊断。对于这些患者,必须谨慎进行辅助医疗护理以避免中空脏器破裂。分子检测可用于确诊,并为家庭成员提供准确的遗传咨询和预测性基因检测。