Donnell Christopher C, McKeague Kelly F, Cooper Aisling, Stenhouse John
Edinburgh Dental Institute, NHS Lothian, United Kingdom.
School of Dentistry, Belfast Health and Social Care Trust, United Kingdom.
Br J Oral Maxillofac Surg. 2020 Jun;58(5):608-610. doi: 10.1016/j.bjoms.2020.03.004. Epub 2020 Mar 20.
Congenital midline nasal lesions are extremely rare, and nasal dermoids are their most common presentation. To the best of our knowledge, only two cases of a philtrum sinus with skull base extension have been reported previously. A 3-year-old boy presented to the maxillofacial department with a discharging upper lip sinus that had been present from birth. No other congenital abnormalities were reported. Initially this sinus was assumed to be blind-ended and excised under general anaesthetic, but the area then failed to heal. Radiological work-up showed a patent dermal sinus that extended from the infranasal region through the nasal septum into the basal aspect of the anterior cranial fossa. The patient was referred for multidisciplinary management. A high index of suspicion of nasofrontal dermoid should be exercised when a patient presents with an upper lip sinus and recurrent discharge, until it is proven otherwise.
先天性中线鼻部病变极为罕见,鼻皮样囊肿是其最常见的表现形式。据我们所知,此前仅报道过两例伴有颅底延伸的人中窦病例。一名3岁男孩因出生时就存在的上唇窦流脓而就诊于颌面科。未报告其他先天性异常情况。起初,这个窦被认为是盲端的,并在全身麻醉下进行了切除,但随后该区域未能愈合。影像学检查显示存在一个开放的皮样窦,从鼻下区域穿过鼻中隔延伸至前颅窝底部。该患者被转诊进行多学科管理。当患者出现上唇窦且反复流脓时,应高度怀疑鼻额部皮样囊肿,除非另有证据证明。