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Gingival hyperplasia as first sign of recurrence of granulomatosis with polyangiitis (Wegener’s granulomatosis): case report and review of the literature

机译:牙龈增生是肉芽肿合并多血管炎(韦格纳肉芽肿)复发的第一个标志:病例报告和文献复习

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Background Granulomatosis with polyangiitis (GPA), formerly referred to as Wegener’s granulomatosis, is a rare systemic disease of unknown etiology which can affect all areas of the body, including the oral cavity. The typical oral manifestations occur as nonspecific erosive/ulcerative lesions of the oral cavity or appear with hyperplastic gingivitis, a so called “strawberry gingivitis”. Case presentation We report here about an extremely rare case with hyperplastic gingivitis as the first sign of recurrence of GPA in the absence of oral manifestations in the primary disease. A 72?year-old female was referred to our Department of Cranio-Maxillofacial Surgery with hyperplastic gingivitis. The patient was diagnosed with GPA already eight years before. We referred the patient to our Clinic of Internal Medicine where she was successfully treated with rituximab. At the follow-up visit, the patient showed complete remission of the hyperplastic gingiva. Conclusion The often overlooked oral manifestation may be interpreted as the first evidence of resurgent GPA in general and therefore could be pathognostic for the disease. This case affirms the need of health professionals to be acquainted with orofacial manifestations of rare diseases such as GPA. As a consequence, dentists will be able to assist in diagnosing GPA more easily leading to a better prognosis for patients suffering from this disease.
机译:背景肉芽肿性多血管炎(GPA),以前称为韦格纳肉芽肿病,是一种病因不明的罕见全身性疾病,可影响包括口腔在内的身体所有区域。典型的口腔表现为口腔的非特异性糜烂/溃疡性病变,或伴有增生性牙龈炎,即所谓的“草莓型牙龈炎”。病例介绍我们在这里报告了一个增生性牙龈炎的极少数病例,这是原发性疾病中没有口服表现的GPA复发的第一个迹象。一名72岁的女性因增生性牙龈炎被转诊至我们的颅颌面部外科。该患者已经在八年前被诊断出患有GPA。我们将患者转诊至我们的内科诊所,在那里她成功接受了利妥昔单抗治疗。在随访中,患者显示出增生性牙龈的完全缓解。结论经常被忽视的口腔表现可能被解释为一般性GPA复发的最初证据,因此可能是对该病的病理诊断。此案肯定了卫生专业人员必须熟悉罕见疾病(例如GPA)的口腔面部表现。结果,牙医将能够更容易地协助诊断GPA,从而为患有这种疾病的患者提供更好的预后。

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