Churg-Strauss syndrome natural history, complications and prognosis: Difference between revisions
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Revision as of 14:19, 25 November 2016
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Churg-Strauss syndrome Microchapters |
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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
Natural History
Classically, three phases of Eosinophilic granulomatosis with polyangiitis are seen. They are distributed as follows:[1]
Stage 1: The Prodromal Phase
This stage occurs in the teenage years through the 20’s. The first stage often involves the sinuses and the new onset of allergies or the worsening of pre-existing allergies (e.g. atopic diseases, allergic rhinitis).
Stage 2: The Eosinophilic Phase
Peripheral blood eosinophilia is now present. There is eosinophilic infiltration of lung and gastrointestinal (GI) tract. The second stage involves the onset of acute asthma. Normally, the person would not have had asthma previously.
People can live for many years in the first two stages before progressing to stage three.
Stage 3: The Vasculitic Phase
The third phase occurs in the 40’s-50’s and involves multiple organ systems in a life-threatening systemic vasculitis of small and medium sized vessels. Stage three is by far the most life threatening and painful. Often the person will develop severe nerve pain in their legs, arms and hands. Purple marks will appear on the skin and often sores will appear in the mouth or nose. The disease will affect the heart and lungs or it will affect the kidneys and liver.
Complications
Complications of Churg-Strauss syndrome depend on the specific organ involved in the disease process.
- Pericarditis
- Myocarditis
- MI
- Heart failure
- Renal failure
- Cerebral hemorrhage
- Gastrointestinal bleeding
- Status asthmaticus
Prognosis
In the past the prognosis of Eosinophilic granulomatosis with polyangiitis was fatal when untreated. Patients who were not treated had an estimated 5 year survival rate of 20 to 30%. Today, the prognosis of Eosinophilic granulomatosis with polyangiitis is heavily dependent on starting treatment with a glucocorticoid.
The following are favorable prognostic factors:[2]
- Early diagnosis of the disease
- Decreased cutaneous involvement
- Elevated C-reactive protein
The following are poor prognostic factors:
| Five-Factor Score Assessment |
|---|
| Proteinuria > 1g/d |
| Creatinine > 140mm/l |
| Cardiomyopathy |
| Severe GI manifestations |
| CNS involvement |
| Five-Factor Score | |
|---|---|
| Score | Mortality Rate |
| 0 | 12% |
| 1 | 26% |
| >2 | 46% |
[3] It has also been concluded that age greater than 65 is also a risk factor for mortality.[4]
References
- ↑ Greco A, Rizzo MI, De Virgilio A, Gallo A, Fusconi M, Ruoppolo G; et al. (2015). "Churg-Strauss syndrome". Autoimmun Rev. 14 (4): 341–8. doi:10.1016/j.autrev.2014.12.004. PMID 25500434.
- ↑ Kim MY, Sohn KH, Song WJ, Park HW, Cho SH, Min KU; et al. (2014). "Clinical features and prognostic factors of Churg-Strauss syndrome". Korean J Intern Med. 29 (1): 85–95. doi:10.3904/kjim.2014.29.1.85. PMC 3932399. PMID 24574837.
- ↑ Guillevin L, Lhote F, Gayraud M; et al. (1996). "Prognostic factors in polyarteritis nodosa and Churg-Strauss syndrome. A prospective study in 342 patients". Medicine (Baltimore). 75 (1): 17–28. PMID 8569467.
- ↑ Guillevin L, Pagnoux C, Seror R, Mahr A, Mouthon L, Le Toumelin P; et al. (2011). "The Five-Factor Score revisited: assessment of prognoses of systemic necrotizing vasculitides based on the French Vasculitis Study Group (FVSG) cohort". Medicine (Baltimore). 90 (1): 19–27. doi:10.1097/MD.0b013e318205a4c6. PMID 21200183.