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特发性中线肉芽肿——当前的分类及治疗争议

Idiopathic midline granuloma--current classification and management controversies.

作者信息

Graper R G, Orenstein H H, Rohrich R J, Byrd H S, Rich B K

机构信息

University of Texas at Southwestern Medical Center at Dallas, Department of Plastic and Reconstructive Surgery 75235-9132, USA.

出版信息

Ann Plast Surg. 1996 Nov;37(5):532-7. doi: 10.1097/00000637-199611000-00013.

Abstract

Midline granuloma is a mutilating process produced by a number of diseases that progressively destroy the nose, paranasal sinuses, and palate. Infectious, neoplastic, and idiopathic forms of this disease have been described. The specific diagnoses must be ascertained, as the treatment is different depending on the etiology of the disease. Radiation therapy is the treatment of choice for idiopathic midline destructive disease, while cytoxan is appropriate for Wegener's granulomatosis, polymorphic reticulosis, and primary nasal lymphomas. When the diagnosis is uncertain, the least-toxic therapy should be used. If the treatment is failing, an alternate therapy should be tried. This article reviews the history of idiopathic midline granuloma, describes the current classification of the disease, and discusses controversial issues demonstrated by two patient presentations.

摘要

中线肉芽肿是由多种疾病引起的一种致残性病变,这些疾病会逐渐破坏鼻子、鼻窦和腭部。已经描述了该疾病的感染性、肿瘤性和特发性形式。必须确定具体诊断,因为治疗方法会因疾病的病因不同而有所差异。放射治疗是特发性中线破坏性疾病的首选治疗方法,而环磷酰胺适用于韦格纳肉芽肿、多形性网状细胞增生症和原发性鼻淋巴瘤。当诊断不确定时,应采用毒性最小的治疗方法。如果治疗失败,应尝试替代疗法。本文回顾了特发性中线肉芽肿的病史,描述了该疾病的当前分类,并讨论了两个病例展示所揭示的争议性问题。

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