Martirosyan Zara, Malhotra Sonal
Department of Sleep Medicine, Baylor College of Medicine, Houston, Texas.
Texas Children's Hospital, Houston, Texas.
J Clin Sleep Med. 2020 Oct 15;16(10):1805-1807. doi: 10.5664/jcsm.8650.
Klippel-Feil sequence (KFS) is a rare congenital condition that presents with congenital cervical spine fusion, reduced cervical spine flexion, and low posterior hairline. Chiari malformation type 1 and sleep-disordered breathing (SDB) are frequent comorbidities of KFS. The pathologic basis of the connection between Chiari malformation type 1 and SDB in the setting of KFS is not clearly understood. Here we report a pediatric patient with KFS, SDB, and drooling who also had Chiari malformation type 1. Posterior fossa decompression of this patient significantly improved most symptoms including sleep disturbances. Repeat polysomnogram 8 weeks after posterior fossa decompression revealed worsening central sleep apnea despite the patient being clinically asymptomatic. Taken together, this case highlights the point that, although it is critical to recognize the association of SDB in the setting of KFS, decompression alone may not be sufficient to completely alleviate SDB and certain neurologic symptoms.
克利佩尔-费尔综合征(KFS)是一种罕见的先天性疾病,表现为先天性颈椎融合、颈椎前屈减少和后发际线低。1型 Chiari 畸形和睡眠呼吸障碍(SDB)是KFS常见的合并症。在KFS背景下,1型 Chiari 畸形与SDB之间联系的病理基础尚不清楚。在此,我们报告一名患有KFS、SDB和流口水症状的儿科患者,其同时还患有1型 Chiari 畸形。该患者的后颅窝减压术显著改善了包括睡眠障碍在内的大多数症状。后颅窝减压术后8周重复进行多导睡眠图检查发现,尽管患者临床无症状,但中枢性睡眠呼吸暂停却加重了。综上所述,该病例凸显了这样一个观点,即尽管认识到KFS背景下SDB的关联至关重要,但仅减压可能不足以完全缓解SDB和某些神经症状。