Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Division of Pediatrics, Section of Dermatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Am J Med Genet A. 2020 Apr;182(4):746-754. doi: 10.1002/ajmg.a.61490. Epub 2020 Jan 21.
Nevus comedonicus syndrome (NCS) is a rare epidermal nevus syndrome characterized by ocular, skeletal, and central nervous system anomalies. We present a 23-month-old boy with a history of a congenital pulmonary airway malformation (CPAM) of the lung and a congenital cataract who developed progressive linear and curvilinear plaques of dilated follicular openings with keratin plugs (comedones) on parts of his scalp, face, and body consistent with nevus comedonicus. MRI of the brain demonstrated an aneurysm of the right internal carotid artery. Genetic testing identified NEK9 c.1755_1757del (p.Thr586del) at mean allele frequency of 28% in the nevus comedonicus. This same mutation was present in the CPAM tissue. This is the first case of a CPAM in a patient with an epidermal nevus syndrome. This case expands the phenotype of nevus comedonicus syndrome to include CPAM and vascular anomalies.
多发性皮脂囊瘤综合征(NCS)是一种罕见的表皮痣综合征,其特征为眼部、骨骼和中枢神经系统异常。我们报告了一例 23 个月大的男婴,该男婴患有先天性肺气道畸形(CPAM)和先天性白内障,其部分头皮、面部和身体出现进行性线状和曲线状扩张的滤泡开口斑块,伴有角蛋白栓(粉刺),符合多发性皮脂囊瘤的表现。脑部 MRI 显示右侧颈内动脉动脉瘤。基因检测在多发性皮脂囊瘤组织中发现了 NEK9 c.1755_1757del(p.Thr586del),其平均等位基因频率为 28%。CPAM 组织中也存在相同的突变。这是首例 CPAM 患者伴发表皮痣综合征。该病例扩展了多发性皮脂囊瘤综合征的表型,包括 CPAM 和血管异常。