Granulomatosis with Polyangiitis: Diagnostic Difficulties and Treatment
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Author:
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MASHKURA RIZAMUKHAMEDOVA, DILDORA NABIYEVA, ELNORA DZHURAYEVA, DILFUZA BERDIEVA, SEVARA MUKHAMMADIEVA
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Abstract:
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The article presents up-to-date data on etiopathogenesis, clinic, diagnostics, differential diagnostics, treatment and prognosis in granulomatosis with polyangiitis (GPA). Early diagnosis of GPA is a difficult clinical task and requires careful examination of the patient using modern research methods to identify pathognomic symptoms. Early detection of anti-neutrophil cytoplasmic antibodies (ANCA) increases the frequency of GPA diagnosis, a biopsy of affected organs allows verifying the diagnosis morphologically.
Only timely establishment of the diagnosis allows prescribing therapy as early as possible and avoiding disability of patients.
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Keyword:
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systemic vasculitis, anti-neutrophil cytoplasmic antibodies, granulomatosis with polyangiitis, diagnosis, treatment.
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EOI:
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-
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DOI:
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https://doi.org/10.31838/ijpr/2020.12.02.0112
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