Churg-Strauss syndrome laboratory findings
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Krzysztof Wierzbicki M.D. [3]
Overview
Laboratory findings consistent with the diagnosis of Eosinophilic granulomatosis with polyangiitis include, antineutrophil cytoplasmic antibodies, hypereosinophilia, and elevated immunoglobulin E titers (IgE).
Laboratory Findings
Laboratory findings consistent with the diagnosis of Eosinophilic granulomatosis with polyangiitis include, antineutrophil cytoplasmic antibodies, hypereosinophilia, and elevated immunoglobulin E titers (IgE). Routine laboratory tests that are used to identify Eosinophilic granulomatosis with polyangiitis are:.[1]
Blood Work-up
- Complete blood count (CBC)
- Uremia
- Serum creatinine
- Blood urea nitrogen (BUN)
- Antineutrophil cytoplasmic antibody test
- Eosinophilia
- Immunoglobulin
- Erythrocyte sedimentation rate (ESR)
- C-reactive protein (CRP)
- Serum troponin[2]
- Rheumatoid factor
Urinalysis
- Proteinuria
- Microscopic hematuria
- Albuminuria
- Red blood cell casts
Biopsy
Renal biopsy is the
References
- ↑ CHURG J, STRAUSS L (1951). "Allergic granulomatosis, allergic angiitis, and periarteritis nodosa". Am J Pathol. 27 (2): 277–301. PMC 1937314. PMID 14819261.
- ↑ McAleavey N, Millar A, Pendleton A (2013). "Cardiac involvement as the main presenting feature in eosinophilic granulomatosis with polyangiitis". BMJ Case Rep. 2013 ( ): . doi:10.1136/bcr-2013-009394. PMC 3736255. PMID 23853013.