From the Departments of *Internal Medicine and †Diagnostic Radiology, Daegu Fatima Hospital, and ‡Department of Internal Medicine, Kyungpook National University Hospital, Daegu, Korea.
J Clin Rheumatol. 2013 Dec;19(8):446-8. doi: 10.1097/RHU.0000000000000036.
Although granulomatosis with polyangiitis (GPA) can affect a large number of organ systems and produce a broad spectrum of clinical symptoms, skeletal involvement is very rare, with the exception of facial bone involvement associated with destructive nasal and sinus inflammation. We describe here a 54-year-old man with sternal osteomyelitis and destructive arthritis around the sternoclavicular joint. Despite antibiotics and conventional immunosuppressive treatment, his symptoms deteriorated, and a new mass-like lung lesion was developed. A histopathologic analysis of the lung mass revealed chronic granulomatous inflammation with fibrinoid necrosis, and he was diagnosed with GPA. When a patient with a destructive inflammatory lesion has negative culture results and no response to conventional therapy, we propose that an aggressive approach is necessary for a pathologic diagnosis to exclude the possibility of GPA.
虽然肉芽肿伴多血管炎(GPA)可影响大量的器官系统并产生广泛的临床症状,但骨骼受累非常罕见,除了与破坏性鼻和鼻窦炎症相关的面部骨受累。我们在此描述了一位 54 岁男性,患有胸骨骨髓炎和胸锁关节周围破坏性关节炎。尽管使用了抗生素和常规免疫抑制治疗,但他的症状恶化,并且出现了新的块状肺病变。对肺块的组织病理学分析显示为伴有纤维蛋白样坏死的慢性肉芽肿性炎症,他被诊断为 GPA。当患有破坏性炎症性病变的患者的培养结果为阴性且对常规治疗无反应时,我们建议需要采取积极的方法进行病理诊断以排除 GPA 的可能性。