Anesth Prog. 2024 Sep 9;71(3):140-144. doi: 10.2344/523400.
Pfeiffer syndrome (PS) is a rare inherited disorder that affects the craniofacial and extremity bones but can also include anomalies of the upper and lower airways. Among the 3 subtypes, PS types 2 and 3 are the most severe. We describe the anesthetic management of a 10-year-old boy with PS type 2 scheduled for dental treatment under general anesthesia. Because of his history of Chiari malformation, avoiding neck hyperextension was recommended to prevent worsening of his neurologic function. Preoperative computed tomography revealed significant nasal stenosis but no tracheal anomalies. Considering the difficulty of nasotracheal intubation, we planned for an oral intubation. General anesthesia was induced using sevoflurane, nitrous oxide, and oxygen along with an oropharyngeal airway. After lidocaine was topically applied to the oropharynx, fiber-optic orotracheal intubation was performed under spontaneous ventilation to minimize head and neck movement. Anesthesia was maintained using desflurane and remifentanil, and no postoperative complications were observed. General anesthesia for patients with PS requires careful planning, which should include preoperative assessment of the airway to determine the feasibility of nasotracheal intubation and identify airway irregularities.
佩弗异常综合征(PS)是一种罕见的遗传性疾病,影响颅面和四肢骨骼,但也可能包括上下气道的异常。在 3 种亚型中,PS 型 2 和 3 最为严重。我们描述了一名 10 岁男孩的麻醉管理情况,该男孩患有 PS 型 2,计划在全身麻醉下进行牙科治疗。由于他有 Chiari 畸形的病史,建议避免颈部过度伸展,以防止神经功能恶化。术前计算机断层扫描显示明显的鼻狭窄,但无气管异常。考虑到经鼻插管的困难,我们计划进行经口插管。全身麻醉采用七氟醚、氧化亚氮和氧气以及口咽气道诱导。利多卡因局部应用于口咽后,在自主通气下进行纤维光导经口气管插管,以最大程度减少头颈部运动。麻醉采用地氟烷和瑞芬太尼维持,未观察到术后并发症。PS 患者的全身麻醉需要仔细计划,包括术前气道评估,以确定经鼻插管的可行性,并确定气道不规则。