de la Monte S M, Dorfman H D, Chandra R, Malawer M
Hum Pathol. 1984 Jun;15(6):551-8. doi: 10.1016/s0046-8177(84)80009-x.
Intraosseous schwannoma, a rare benign neoplasm, has a characteristic radiographic appearance. The histologic features, although similar to those of soft tissue schwannomas, may be obscure when the lesions are highly cellular and the Antoni Types A and B patterns are subtle. Four additional cases of intraosseous schwannoma are presented, with ultrastructural studies from two tumors, one of which was highly cellular and presented a diagnostic problem. The ultrastructural features of intraosseous schwannomas have not been documented previously; however, the findings are essentially the same as those observed in soft tissue schwannomas. The radiographic, histologic, and ultrastructural findings in the cases reported are discussed in relation to published data for intraosseous and soft tissue schwannomas. The authors propose that the comparatively high frequency of mandibular involvement by intraosseous schwannoma may be related to the fact that schwannomas, in general, arise most frequently in the head and neck regions. Furthermore, since schwannomas arise mainly in association with sensory nerves, probably the dearth of such fibers within bone accounts for the rarity of intraosseous schwannoma.
骨内神经鞘瘤是一种罕见的良性肿瘤,具有特征性的影像学表现。其组织学特征虽然与软组织神经鞘瘤相似,但当病变细胞丰富且Antoni A型和B型结构不明显时,可能难以辨认。本文报告了另外4例骨内神经鞘瘤,并对其中2例肿瘤进行了超微结构研究,其中1例细胞丰富,存在诊断难题。骨内神经鞘瘤的超微结构特征此前尚未见报道;然而,其结果与软组织神经鞘瘤基本相同。本文结合已发表的骨内和软组织神经鞘瘤数据,讨论了所报告病例的影像学、组织学和超微结构表现。作者提出,骨内神经鞘瘤下颌骨受累相对频繁,可能与神经鞘瘤通常最常发生于头颈部区域这一事实有关。此外,由于神经鞘瘤主要与感觉神经相关,可能骨内此类纤维的缺乏导致了骨内神经鞘瘤的罕见。