McGuire Duncan, Mielke Nicholas, Bahl Amit
Beaumont Hospital, Department of Emergency Medicine, Royal Oak, Michigan.
Oakland University William Beaumont School of Medicine, Department of Emergency Medicine, Royal Oak, Michigan.
Clin Pract Cases Emerg Med. 2022 Aug;6(3):229-231. doi: 10.5811/cpcem.2022.4.56488.
Carotid artery dissection is a rare but serious condition manifesting with signs and symptoms that closely overlap with other more benign medical diagnoses. This vascular injury, however, can result in debilitating sequelae, including thromboembolic cerebrovascular accidents.
We describe the atypical presentation of a healthy eight-year-old male who presented to the emergency department (ED) with generalized abdominal pain and non-bloody, non-bilious emesis. These symptoms occurred nine days after he sustained blunt head trauma after a non-syncopal fall from standing while playing hockey. He was initially diagnosed with gastroesophageal reflux disease and constipation and was discharged home. The following day he developed an acute headache followed shortly by gait ataxia, prompting a return visit to the ED. Imaging of the head and neck revealed a left internal carotid artery dissection. The patient was started on intravenous unfractionated heparin and admitted to the hospital. He was later discharged symptom-free on therapeutic enoxaparin for eight weeks, followed by daily aspirin therapy.
Pediatric trauma patients, especially those sustaining insult to the head and cervical spine, are at risk for craniocervical arterial injuries. This rare but dangerous pathology often manifests in a non-specific, delayed fashion making it a challenging diagnosis for physicians to make on the initial medical encounter. Maintaining a high clinical suspicion for carotid artery dissection is required to make this diagnosis and should guide a thorough history, physical examination, and appropriate imaging in order to improve patient morbidity and mortality. This case emphasizes key clinical features and risk factors of this disease that may help emergency clinicians promptly recognize and treat this entity.
颈动脉夹层是一种罕见但严重的疾病,其体征和症状与其他更良性的医学诊断有密切重叠。然而,这种血管损伤可导致使人衰弱的后遗症,包括血栓栓塞性脑血管意外。
我们描述了一名健康8岁男性的非典型表现,他因全身腹痛和非血性、非胆汁性呕吐到急诊科就诊。这些症状发生在他在打曲棍球时从站立状态非晕厥性摔倒导致头部钝器伤九天后。他最初被诊断为胃食管反流病和便秘,随后出院回家。第二天,他出现急性头痛,不久后出现步态共济失调,促使他再次前往急诊科就诊。头颈部影像学检查显示左侧颈内动脉夹层。患者开始静脉注射普通肝素并住院治疗。他后来在接受了八周的治疗性依诺肝素治疗且症状消失后出院,随后接受每日阿司匹林治疗。
儿科创伤患者,尤其是那些头部和颈椎受到损伤的患者,有发生颅颈动脉损伤的风险。这种罕见但危险的病理情况通常以非特异性、延迟的方式表现出来,这使得医生在初次接诊时难以做出诊断。要做出这种诊断需要高度怀疑颈动脉夹层,并应指导全面的病史询问、体格检查和适当的影像学检查,以改善患者的发病率和死亡率。本病例强调了这种疾病的关键临床特征和危险因素,可能有助于急诊临床医生及时识别和治疗该疾病。