Abstract
GPA is a rare disease with reported annual incidence and prevalence is estimated 23.7-156.5 per million and 3.0-14.4 per million, respectively (1). GPA is more common in European populations and slightly more in male with male to female ratio 1.5: 1 (2). It may occur at any age but typically at age 35-55 years old. It classically involved upper and lower respiratory tract and glomerulonephritis. According to American College of Rheumatology (ACR) classification the diagnosis is made when 2 out of 4 criteria are present, which includes nasal or oral inflammation, abnormal chest radiograph, urinary sediment and granulomatous inflammation on biopsy. This test has a sensitivity of 88.2 percent and specificity of92 percent.
Otological manifestation are found in 19 to 61 percent of cases with GP A (3 ). The commonest presentation is otitis media ( 4). It is due to eustachian tube dysfunction caused by nasopharyngeal involvement but commonly misdiagnosed as infection (5). Up to 50 percent of GPA cases presented with hearing loss ( 6). Bakthavachalam et al reported that both sensorineural and conductive hearing loss are common in GP A (7). However, audiogram was not done for our patient to determine the type of hearing loss.
Metadata
Item Type: | Thesis (Masters) |
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Creators: | Creators Email / ID Num. Mustapa Albakari, Nabia Idaam nabiaidaam@yahoo.com.my |
Subjects: | Q Science > QM Human anatomy > Vascular System Q Science > QP Physiology > Heart R Medicine > RD Surgery > Surgery by region, system, or organ > Cardiovascular system |
Divisions: | Universiti Teknologi MARA, Selangor > Sungai Buloh Campus > Faculty of Medicine |
Programme: | MMed |
Keywords: | granulomatosis, polyangiitis, hearing loss |
Date: | October 2018 |
URI: | https://ir.uitm.edu.my/id/eprint/67012 |
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