Linkov Gary, Kanev Paul M, Isaacson Glenn
Department of Otolaryngology - Head & Neck Surgery and Temple University School of Medicine, Philadelphia, PA 19140, USA.
Department of Neurosurgery, University of Connecticut School of Medicine, Connecticut Children's Medical Center, Hartford, CT 06106, USA.
Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1810-3. doi: 10.1016/j.ijporl.2015.08.006. Epub 2015 Aug 13.
Congenital dermoid cysts of the skull and face frequently arise in embryonic fusion planes. They may follow these planes to extend intratemporally or intracranially. Advanced imaging and operative techniques are generally recommended for these lesions. Postauricular temporal bone dermoid cysts seem to form a distinct subgroup with a lesser tendency toward deep extension. They may be amenable to more conservative management strategies.
With IRB-approval, we queried a prospectively-accrued computerized patient-care database to find all postauricular temporal dermoid lesions surgically managed by a single pediatric otolaryngologist from 2001 to 2014. We reviewed the English-language literature to identify similar series of surgically treated pediatric temporal bone dermoid cysts.
Ten postauricular temporal dermoid cysts with pathological confirmation were identified in our surgical series. The average size of the lesions was 1.5 cm (0.3-3 cm). The average age at time of surgery was 4 years (6 months-17 years). No intracranial extension was observed at surgery. There were no recurrences noted on last follow-up (mean 65 months, range 10-150 months). A computerized literature review found no examples of intracranial extension among typical postauricular dermoid cysts.
There was no intracranial or temporal extension in our series or among postauricular lesions described in the literature. Given the low incidence of deep extension we advocate neither advanced imaging nor routine neurosurgical consultation for typical postauricular lesions. Dissection in continuity with cranial periosteum facilitates intact removal of adherent lesions. Surgery is curative if the dermoid is removed intact.
颅骨和面部的先天性皮样囊肿常出现在胚胎融合平面。它们可能沿着这些平面颞内或颅内延伸。对于这些病变,一般推荐采用先进的影像学和手术技术。耳后颞骨皮样囊肿似乎形成一个独特的亚组,向深部延伸的倾向较小。它们可能适合更保守的治疗策略。
经机构审查委员会批准,我们查询了一个前瞻性积累的计算机化患者护理数据库,以找出2001年至2014年由一名儿科耳鼻喉科医生手术治疗的所有耳后颞部皮样病变。我们查阅了英文文献,以确定类似的一系列手术治疗的儿科颞骨皮样囊肿。
在我们的手术系列中,发现了10例经病理证实的耳后颞部皮样囊肿。病变的平均大小为1.5厘米(0.3 - 3厘米)。手术时的平均年龄为4岁(6个月 - 17岁)。手术中未观察到颅内延伸。最后一次随访时未发现复发(平均65个月,范围10 - 150个月)。计算机化文献综述发现,典型耳后皮样囊肿中没有颅内延伸的例子。
在我们的系列以及文献中描述的耳后病变中,均未发现颅内或颞部延伸。鉴于深部延伸的发生率较低,对于典型的耳后病变,我们既不主张进行先进的影像学检查,也不主张进行常规的神经外科会诊。与颅骨骨膜连续剥离有助于完整切除粘连的病变。如果皮样囊肿完整切除,手术可治愈。