Charles P D, Fenichel G M
Department of Neurology, Vanderbilt University School of Medicine, Nashville, TN 37212-3375.
Pediatr Neurol. 1994 May;10(3):262-3. doi: 10.1016/0887-8994(94)90037-x.
A child suffered bilateral thalamic infarction secondary to Sneddon and antiphospholipid antibody syndromes. Her initial findings of hypersomnolence, mood disturbance, and amnesia are characteristic of bilateral thalamic infarction. Clinical and laboratory evaluation confirmed the diagnosis of both Sneddon and antiphospholipid antibody syndromes as the cause of her unusual stroke. The treatment of this patient, based on experience with adult patients, was long-term, high-intensity warfarin anticoagulation.
一名儿童因斯内登综合征和抗磷脂抗体综合征继发双侧丘脑梗死。她最初出现的嗜睡、情绪障碍和失忆是双侧丘脑梗死的典型表现。临床和实验室评估证实,斯内登综合征和抗磷脂抗体综合征均为其罕见中风的病因。基于对成年患者的治疗经验,该患者接受了长期、高强度的华法林抗凝治疗。