Benign solitary neurilemoma (Schwannoma). A correlative cytological and histological study of 28 cases.

I. Dahl, B. Hagmar, I. Idvall
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引用次数: 51

Abstract

A correlative histological and cytological study of 28 cases of solitary neurilemoma is presented. The typical histological mixture of Antoni type A and B tissue correlated well with the cytological findings. In the smears, the Antoni type A tissue was represented by tissue fragments with a fibrillar ground substance and slender, spindle-shaped cells forming obvious Verocay bodies in 24 cases, and the Antoni type B tissue by loose, microcystic fragments with single, elongated nuclei sometimes looking like fish-hooks and with indistinct, slender, cytoplasmic processes. The ancient neurilemomas, a variant of the ordinary neurilemomas, in this series were characterised both histologically and cytologically by nuclear hyperchromasia and polymorphism, which it is important to be aware of in order to avoid an erroneous diagnosis of sarcoma or probable sarcoma. The differential diagnosis is discussed and it is concluded that diagnosis of neurilemoma by fine-needle aspiration biopsy is possible, particularly when Verocay bodies and/or a fibrillar ground substance are present in the smears. It is stressed that fine-needle aspiration biopsy is an important aid to pre-operative diagnosis of neurilemoma, and thus to planning of the operative treatment.
良性孤立神经鞘瘤(神经鞘瘤)。28例相关细胞学和组织学研究。
本文报告28例孤立性神经鞘瘤的组织学和细胞学研究。典型的Antoni A型和B型组织的组织学混合与细胞学结果有很好的相关性。24例Antoni A型组织以纤维状基质和细长梭形细胞组成明显的Verocay小体的组织碎片为代表,Antoni B型组织以松散的微囊状碎片为代表,细胞核单一,伸长,有时看起来像鱼钩,细胞质突起模糊,细长。古老的神经鞘瘤是普通神经鞘瘤的一种变体,在这个系列中,在组织学和细胞学上都表现为核染色增多和多态性,为了避免肉瘤或可能的肉瘤的错误诊断,重要的是要注意这一点。我们讨论了鉴别诊断,并得出结论,细针穿刺活检诊断神经鞘瘤是可能的,特别是当在涂片中存在Verocay体和/或纤维状基底物质时。强调细针穿刺活检是神经鞘瘤术前诊断的重要辅助手段,有助于制定手术治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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