Butler Randall T, Patel Rajiv M, McHugh Jonathan B
Department of Pathology, University of Michigan, Ann Arbor, MI, USA.
Head Neck Pathol. 2016 Sep;10(3):286-91. doi: 10.1007/s12105-016-0680-2. Epub 2016 Jan 8.
While head and neck sites comprise the most common location of schwannomas, clinicopathologic data regarding those tumors occurring in non-acoustic and non-cutaneous locations are relatively sparse. In this study, therefore, we sought to examine retrospectively the clinical and pathologic features of head and neck schwannomas excised at our institution over a 20-year period. During this period, we identified a total cohort of 85 patients, which included 36 males (42.4 %) and 49 females with average age of 41.3 years, the majority of which presented asymptomatically with a mass. Localized symptoms were, however, associated with all of the schwannomas that arose in the oral cavity and larynx, while tumors within or adjacent to bone were often associated with neurologic complaints (7 of 15 such tumors [46.7 %]). Clinical follow-up data was available in 86.4 % of all cases and demonstrated no recurrences or mortality. Pathologically, the microscopic features were characteristic of those well-described for schwannomas in other sites, including alternating Antoni A and B areas and the presence of degenerative changes. Tumor encapsulation, however, was variable and was completely absent in schwannomas of the nasal cavity, paranasal sinuses, and larynx. Additionally, a significant minority of the tumors (28.2 %) exhibited foci that resembled neurofibroma. Non-acoustic, non-cutaneous schwannomas of the head and neck appear to have clinicopathologic features similar to their soft tissue counterparts with some subsite variation in presentation and/or microscopic features.
虽然头颈部是神经鞘瘤最常见的发生部位,但关于非听神经和非皮肤部位发生的神经鞘瘤的临床病理数据相对较少。因此,在本研究中,我们回顾性研究了在我们机构20年间切除的头颈部神经鞘瘤的临床和病理特征。在此期间,我们共确定了85例患者,其中包括36名男性(42.4%)和49名女性,平均年龄为41.3岁,大多数患者无症状,仅表现为肿块。然而,所有发生在口腔和喉部的神经鞘瘤均伴有局部症状,而位于骨内或骨旁的肿瘤常伴有神经症状(15例此类肿瘤中有7例[46.7%])。86.4%的病例有临床随访数据,均未发现复发或死亡。病理上,显微镜下特征与其他部位神经鞘瘤所描述的特征一致,包括交替出现的Antoni A区和B区以及退行性改变。然而,肿瘤包膜情况不一,鼻腔、鼻窦和喉部的神经鞘瘤完全没有包膜。此外,少数肿瘤(28.2%)表现出类似神经纤维瘤的病灶。头颈部非听神经、非皮肤神经鞘瘤似乎具有与其软组织对应物相似的临床病理特征,在表现和/或显微镜特征上存在一些亚部位差异。