面瘫伴舌溃疡:肉芽肿病伴多血管炎的罕见首发表现

IF 0.1 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Archives of Orofacial Science Pub Date : 2022-06-23 DOI:10.21315/aos2022.1701.cr01
Ainiyah Nur, Mohd Shawal Firdaus Mohamad, Noor Afidah Abdullah, G. Tan, A. Mawaddah
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引用次数: 0

摘要

肉芽肿伴多血管炎(GPA)是一种罕见的多系统疾病。虽然GPA很罕见,但它通常出现在局部阶段,在发展到全身阶段之前,其表现涉及上呼吸道或下呼吸道。因此,大多数GPA患者会去看口腔外科医生或耳鼻喉科医生寻求治疗。然而,由于GPA在常见口腔和面部疾病中不常被视为鉴别诊断,因此GPA的诊断经常被推迟。缺乏诊断GPA的金标准调查,这使得该病例的管理成为一个诊断难题。我们在此报告一名患者,他被诊断为双侧急性中耳炎和左乳突炎并伴有面神经麻痹,后来在首次就诊一个月后出现舌头溃疡。耳朵、面部和口腔症状代表了GPA全面发展阶段的诊断转移注意力。
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Facial Palsy with Tongue Ulcer: A Rare Initial Presentation of Granulomatosis with Polyangiitis
Granulomatosis with polyangiitis (GPA) is a rare multisystem disease. Although GPA is rare, it commonly presents in a localised stage where its manifestation involves the upper or lower respiratory tract before progressing to a generalised stage. Therefore, most patients with GPA will visit an oral surgeon or an otolaryngologist to seek treatment. However, the diagnosis of GPA is often delayed as GPA is not frequently considered as a differential diagnosis in common oral and facial diseases. The lack of gold standard investigation for the diagnosis of GPA makes management of this case, a diagnostic conundrum. We herein report a patient who was diagnosed with bilateral acute otitis media and left mastoiditis complicated with facial nerve palsy, and later developed tongue ulceration one month after his initial presentation. The ear, facial and oral symptoms represent a diagnostic red herring to a fullblown generalised stage of GPA.
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来源期刊
Archives of Orofacial Science
Archives of Orofacial Science DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
0.30
自引率
50.00%
发文量
27
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