Wegener's granulomatosis: challenges in making the diagnosis- a case report
被引:0
|
作者:
Mohamad, Siti Dayana
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h-index: 0
机构:
Univ Sains Malaysia, Sch Med Sci, Dept Radiol, Kota Baharu 16150, Kelantan, MalaysiaUniv Sains Malaysia, Sch Med Sci, Dept Radiol, Kota Baharu 16150, Kelantan, Malaysia
Mohamad, Siti Dayana
[1
]
Ahmad, Muhamad Zabidi
论文数: 0引用数: 0
h-index: 0
机构:
Univ Sains Malaysia, Adv Med & Dent Inst, Dept Imaging, Kepala Batas 13200, Penang, MalaysiaUniv Sains Malaysia, Sch Med Sci, Dept Radiol, Kota Baharu 16150, Kelantan, Malaysia
Ahmad, Muhamad Zabidi
[2
]
机构:
[1] Univ Sains Malaysia, Sch Med Sci, Dept Radiol, Kota Baharu 16150, Kelantan, Malaysia
[2] Univ Sains Malaysia, Adv Med & Dent Inst, Dept Imaging, Kepala Batas 13200, Penang, Malaysia
来源:
KUWAIT MEDICAL JOURNAL
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2024年
/
56卷
/
03期
关键词:
granulomatosis with polyangiitis;
lung lesion;
Wegener's granulomatosis;
D O I:
暂无
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Wegener's granulomatosis is a rare multi systemic illness with unclear aetiology. It can present with various signs and symptoms with involvement of multiple organ systems. Here, we present a case of a 45-year-old male who presented with multiple episodes of epistaxis. Upon subsequent follow up, he also developed right facial nerve palsy and bilateral mixed hearing loss. Subsequently, there was incidental findings of opacities on chest radiograph, which did not resolve with antibiotics treatment. Computed tomography thorax was performed, which revealed features suggestive of lung malignancy. Lung biopsy finally revealed a diagnosis of Wegener's granulomatosis (WG). This case is particularly interesting due to the diverse presenting symptoms, radiological findings mimicking other pathology and lastly the diagnosis of WG upon histopathology result.