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鼻旁窦道中线破坏性病变:基于组织病理学标准的简化术语

Midline destructive lesions of the sinonasal tract: simplified terminology based on histopathologic criteria.

作者信息

Borges A, Fink J, Villablanca P, Eversole R, Lufkin R

机构信息

Department of Radiological Sciences, University of California, Los Angeles, USA.

出版信息

AJNR Am J Neuroradiol. 2000 Feb;21(2):331-6.

Abstract

BACKGROUND AND PURPOSE

Destructive lesions of the sinonasal tract, lacking a discernible etiology and referred to as midline destructive disease, have been pathologically classified in accordance with a variety of confusing terms. Development of new pathologic concepts and immunohistochemical techniques has provided a fresh understanding of these lesions, and, as a result, they can be unified into two distinct pathologic groups: Wegener's granulomatosis and non-Hodgkin's T-cell lymphoma.

METHODS

We retrospectively reviewed the imaging studies and pathologic specimens of seven patients with prior diagnoses included in the midline destructive disease group. The specimens were reviewed by an oral pathologist using currently accepted pathologic criteria and the newly available immunohistochemical markers CD20, CD45, and CD45RO. Lesions were classified as non-Hodgkin's T-cell lymphomas when positive for CD45 and CD45RO and negative for CD20, and as Wegener's granulomatosis in the presence of noncaseating multinucleated giant cell granulomas and necrotizing vasculitis.

RESULTS

Three of the lesions were reclassified as Wegener's granulomatosis and four as T-cell lymphomas after applying these pathologic criteria. There were no distinguishing imaging findings between Wegener's granulomatosis and non-Hodgkin's T-cell lymphoma.

CONCLUSION

The current pathologic classification for midline destructive disease should be incorporated into the radiologic lexicon and the use of terms from the old classification system, such as idiopathic midline granuloma and lethal midline granuloma, should be abandoned and no longer be used in radiologic reports.

摘要

背景与目的

鼻窦道的破坏性病变,缺乏可辨别的病因,被称为中线破坏性疾病,其病理分类一直依据各种令人困惑的术语。新病理概念和免疫组化技术的发展为这些病变提供了新的认识,结果是,它们可被统一分为两个不同的病理组:韦格纳肉芽肿和非霍奇金T细胞淋巴瘤。

方法

我们回顾性分析了中线破坏性疾病组中7例先前已确诊患者的影像学研究和病理标本。标本由口腔病理学家根据当前公认的病理标准以及新可用的免疫组化标志物CD20、CD45和CD45RO进行复查。当CD45和CD45RO呈阳性而CD20呈阴性时,病变被分类为非霍奇金T细胞淋巴瘤;在存在非干酪样多核巨细胞肉芽肿和坏死性血管炎时,病变被分类为韦格纳肉芽肿。

结果

应用这些病理标准后,3例病变被重新分类为韦格纳肉芽肿,4例被分类为T细胞淋巴瘤。韦格纳肉芽肿和非霍奇金T细胞淋巴瘤之间没有明显的影像学表现。

结论

中线破坏性疾病的当前病理分类应纳入放射学术语中,旧分类系统中的术语,如特发性中线肉芽肿和致死性中线肉芽肿,应被摒弃,不再用于放射学报告。

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