Vora Niraj, Kalagiri Ram, Guillory Bryan, Shetty Ashita, Raju Venkata Nakta, Powitzky R K, Beeram Madhava R
Division of Neonatology, Department of Pediatrics (Vora, Kalagiri, Shetty, Raju, Beeram), Department of Pathology (Guillory), and Department of Pediatric Otolaryngology (Powitzky), Baylor Scott & White Health and Texas A&M Health Science Center College of Medicine, Temple, Texas.
Proc (Bayl Univ Med Cent). 2017 Oct;30(4):459-460. doi: 10.1080/08998280.2017.11930229.
Congenital midline nasal anomalies are rare, with a prevalence of 1 in 20,000 to 40,000 births and with 5% to 7% of them being nasal glioma. Differential diagnoses of nasal anomalies include nasal dermoid cysts, gliomas, encephaloceles, nasal polyps, and some other rare anomalies. Due to current medical technological advancements, most of these anomalies are easily correctable, though delaying management may lead to fatal effects. This report describes two cases-one of nasal glioma and one of nevus lipomatosus cutaneous superficialis-that presented as respiratory distress in a newborn. Approximately 10 to 20 cases of these two conditions have been described; notably, this is the second documented case of nevus lipomatosus cutaneous superficialis with nasal presentation.
先天性中线鼻畸形较为罕见,在每20000至40000例出生婴儿中的发生率为1例,其中5%至7%为鼻胶质瘤。鼻畸形的鉴别诊断包括鼻皮样囊肿、胶质瘤、脑膨出、鼻息肉以及其他一些罕见畸形。由于当前医学技术的进步,这些畸形大多易于矫正,不过延迟治疗可能会导致致命后果。本报告描述了两例病例——一例鼻胶质瘤和一例浅表性皮肤脂肪瘤痣——均表现为新生儿呼吸窘迫。这两种病症大约已报道过10至20例;值得注意的是,这是第二例有文献记载的伴有鼻部表现的浅表性皮肤脂肪瘤痣病例。