Devaney K O, Travis W D, Hoffman G, Leavitt R, Lebovics R, Fauci A S
Department of Pathology, Bethesda Naval Hospital, Maryland.
Am J Surg Pathol. 1990 Jun;14(6):555-64. doi: 10.1097/00000478-199006000-00006.
The majority of patients with classic Wegener's granulomatosis present with symptoms of head and neck disease; accordingly, accurate interpretation of biopsy specimens from these sites is essential. This report details the histologic findings in 126 head and neck biopsy specimens from 70 patients (36 male and 34 female). Tissues were obtained from the following sites: 60 nasal, 27 paranasal sinuses, 17 laryngeal, five periorbital, five oral, four middle ear, three mastoid, two external ear, and three salivary gland. Vasculitis, necrosis, and granulomatous inflammation together were seen in only 16% of all head and neck biopsy specimens. Both vasculitis and granulomatous inflammation were seen in 21% and vasculitis and necrosis in 23% of the biopsy specimens reviewed. We discuss the problems in differential diagnosis, particularly the importance of excluding granulomatous infectious processes, which can imitate the histopathologic features of Wegener's granulomatosis. Based on this study, we propose criteria for the diagnosis of Wegener's granulomatosis based on biopsy specimens from the head and neck region.
大多数典型韦格纳肉芽肿患者表现为头颈部疾病症状;因此,准确解读这些部位的活检标本至关重要。本报告详细介绍了70例患者(36例男性和34例女性)的126份头颈部活检标本的组织学 findings。组织取自以下部位:60份鼻腔、27份鼻窦、17份喉部、5份眶周、5份口腔、4份中耳、3份乳突、2份外耳和3份唾液腺。在所有头颈部活检标本中,血管炎、坏死和肉芽肿性炎症同时出现的情况仅占16%。在复查的活检标本中,21%可见血管炎和肉芽肿性炎症,23%可见血管炎和坏死。我们讨论了鉴别诊断中的问题,特别是排除肉芽肿性感染性疾病的重要性,这些疾病可模仿韦格纳肉芽肿的组织病理学特征。基于本研究,我们提出了基于头颈部区域活检标本诊断韦格纳肉芽肿的标准。