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[中线肉芽肿。结合3例个人病例报告对文献进行综述,特别提及诊断和治疗问题]

[Midline granuloma. A review of the literature with particular reference to diagnostic and therapeutic problems supplemented by 3 personal case reports].

作者信息

Schlegel R, Kraft R

出版信息

HNO. 1979 Oct;27(10):334-44.

PMID:393665
Abstract

The term midline granuloma and various synonyms have been used to describe a rare lesion that ultimately forms a necrotizing ulcerating destruction of the midface. The aetiology has been variously and repeatedly discussed, and a review of the literature shows that at least three entities, which are difficult to differentiate, should be considered. Wegener's granulomatosis, malignant lymphoma and atypical histiocytic lymphoma, a disease with a pleomorphic histology, may all have an extensive necrosis and an intense inflammatory reaction. Upon the diagnosis, which is confirmed by biopsy, depends the appropriate treatment of these fatal diseases. The collective term midline granuloma should be avoided since it may delay the correct management.

摘要

术语“中线肉芽肿”及各种同义词已被用于描述一种罕见病变,该病变最终会导致面部中部出现坏死性溃疡性破坏。其病因已被反复且多样地讨论过,文献综述表明,至少有三种难以区分的实体应被考虑在内。韦格纳肉芽肿、恶性淋巴瘤以及非典型组织细胞淋巴瘤(一种具有多形性组织学表现的疾病)都可能出现广泛坏死和强烈炎症反应。这些致命疾病的恰当治疗取决于经活检确认的诊断结果。应避免使用“中线肉芽肿”这一统称,因为它可能会延误正确的治疗。

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