Churg-Strauss syndrome history and symptoms: Difference between revisions

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Revision as of 14:29, 4 April 2018

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Chandrakala Yannam, MD [3]

Overview

The majority of patients with [disease name] are asymptomatic.

OR

The hallmark of [disease name] is [finding]. A positive history of [finding 1] and [finding 2] is suggestive of [disease name]. The most common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3]. Common symptoms of [disease] include [symptom 1], [symptom 2], and [symptom 3]. Less common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3].

History and Symptoms

Obtaining a complete history is an important aspect in making a diagnosis of eosinophilic granulomatosis with polyangiitis. As it can help differentiate between the ANCA associated vasculitis and other possible causes that may mimic the disease.
Symptoms of eosinophilic granulomatosis with polyangiitis typically develops through three phases, include prodromal phase, eosinophilic phase, and vasculitis phase. Although these phases cannot be clinically distinguishable.^[1]^[2]^[3]^[4]
- Prodromal phase: Most common manifestations include allergic rhinitis and asthma.
- Eosinophilic phase: This phase is characterized by peripheral eosinophilia and infiltration of eosinophils in multiple organs. Most commonly involved organs are lung and GI tract.
- Vasculitic phase: This phase is characterized by small and medium-sized vasculitis and inflammatory granuloma formation. Granulomas can be either vascular or extravascular. Commonly involved organs include lungs, kidneys, skin, heart, and peripheral nerves.

History

Patients with [disease name]] may have a positive history of:

[History finding 1]
[History finding 2]
[History finding 3]

Common Symptoms

Common symptoms of [disease] include:

[Symptom 1]
[Symptom 2]
[Symptom 3]

Less Common Symptoms

Less common symptoms of [disease name] include

[Symptom 1]
[Symptom 2]
[Symptom 3]

References

↑ Lanham JG, Elkon KB, Pusey CD, Hughes GR (March 1984). "Systemic vasculitis with asthma and eosinophilia: a clinical approach to the Churg-Strauss syndrome". Medicine (Baltimore). 63 (2): 65–81. PMID 6366453.
↑ Guillevin L, Cohen P, Gayraud M, Lhote F, Jarrousse B, Casassus P (January 1999). "Churg-Strauss syndrome. Clinical study and long-term follow-up of 96 patients". Medicine (Baltimore). 78 (1): 26–37. PMID 9990352.
↑ Oh MJ, Lee JY, Kwon NH, Choi DC (April 2006). "Churg-Strauss syndrome: the clinical features and long-term follow-up of 17 patients". J. Korean Med. Sci. 21 (2): 265–71. doi:10.3346/jkms.2006.21.2.265. PMC 2734002. PMID 16614512.
↑ Greco A, Rizzo MI, De Virgilio A, Gallo A, Fusconi M, Ruoppolo G, Altissimi G, De Vincentiis M (April 2015). "Churg-Strauss syndrome". Autoimmun Rev. 14 (4): 341–8. doi:10.1016/j.autrev.2014.12.004. PMID 25500434.

Template:WH Template:WS

[pmid6366453-1] Lanham JG, Elkon KB, Pusey CD, Hughes GR (March 1984). "Systemic vasculitis with asthma and eosinophilia: a clinical approach to the Churg-Strauss syndrome". Medicine (Baltimore). 63 (2): 65–81. PMID 6366453.

[pmid9990352-2] Guillevin L, Cohen P, Gayraud M, Lhote F, Jarrousse B, Casassus P (January 1999). "Churg-Strauss syndrome. Clinical study and long-term follow-up of 96 patients". Medicine (Baltimore). 78 (1): 26–37. PMID 9990352.

[pmid16614512-3] Oh MJ, Lee JY, Kwon NH, Choi DC (April 2006). "Churg-Strauss syndrome: the clinical features and long-term follow-up of 17 patients". J. Korean Med. Sci. 21 (2): 265–71. doi:10.3346/jkms.2006.21.2.265. PMC 2734002. PMID 16614512.

[pmid25500434-4] Greco A, Rizzo MI, De Virgilio A, Gallo A, Fusconi M, Ruoppolo G, Altissimi G, De Vincentiis M (April 2015). "Churg-Strauss syndrome". Autoimmun Rev. 14 (4): 341–8. doi:10.1016/j.autrev.2014.12.004. PMID 25500434.

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[2]

[3]

[4]

@@ Line 10: / Line 10: @@
 ==History and Symptoms==
-*Obtaining a complete history is an important aspect in making a diagnosis of eosinophilic granulomatosis with polyangiitis. As it can help differentiate between the ANCA associated vasculitis and other possible causes that may mimic the disease.
+*Obtaining a complete history is an important aspect in making a diagnosis of [[eosinophilic granulomatosis with polyangiitis]]. As it can help differentiate between the [[Anti-neutrophil cytoplasmic antibody|ANCA]] associated [[vasculitis]] and other possible causes that may mimic the [[disease]].
-*Symptoms of eosinophilic granulomatosis with polyangiitis typically develops through three phases, include prodromal phase, eosinophilic phase, and vasculitis phase. Although these phases cannot be distinguishable.<ref name="pmid6366453">{{cite journal |vauthors=Lanham JG, Elkon KB, Pusey CD, Hughes GR |title=Systemic vasculitis with asthma and eosinophilia: a clinical approach to the Churg-Strauss syndrome |journal=Medicine (Baltimore) |volume=63 |issue=2 |pages=65–81 |date=March 1984 |pmid=6366453 |doi= |url=}}</ref><ref name="pmid9990352">{{cite journal |vauthors=Guillevin L, Cohen P, Gayraud M, Lhote F, Jarrousse B, Casassus P |title=Churg-Strauss syndrome. Clinical study and long-term follow-up of 96 patients |journal=Medicine (Baltimore) |volume=78 |issue=1 |pages=26–37 |date=January 1999 |pmid=9990352 |doi= |url=}}</ref><ref name="pmid16614512">{{cite journal |vauthors=Oh MJ, Lee JY, Kwon NH, Choi DC |title=Churg-Strauss syndrome: the clinical features and long-term follow-up of 17 patients |journal=J. Korean Med. Sci. |volume=21 |issue=2 |pages=265–71 |date=April 2006 |pmid=16614512 |pmc=2734002 |doi=10.3346/jkms.2006.21.2.265 |url=}}</ref><ref name="pmid25500434">{{cite journal |vauthors=Greco A, Rizzo MI, De Virgilio A, Gallo A, Fusconi M, Ruoppolo G, Altissimi G, De Vincentiis M |title=Churg-Strauss syndrome |journal=Autoimmun Rev |volume=14 |issue=4 |pages=341–8 |date=April 2015 |pmid=25500434 |doi=10.1016/j.autrev.2014.12.004 |url=}}</ref>
+*[[Symptom|Symptoms]] of [[eosinophilic granulomatosis with polyangiitis]] typically develops through three phases, include prodromal phase, eosinophilic phase, and vasculitis phase. Although these phases cannot be clinically distinguishable.<ref name="pmid6366453">{{cite journal |vauthors=Lanham JG, Elkon KB, Pusey CD, Hughes GR |title=Systemic vasculitis with asthma and eosinophilia: a clinical approach to the Churg-Strauss syndrome |journal=Medicine (Baltimore) |volume=63 |issue=2 |pages=65–81 |date=March 1984 |pmid=6366453 |doi= |url=}}</ref><ref name="pmid9990352">{{cite journal |vauthors=Guillevin L, Cohen P, Gayraud M, Lhote F, Jarrousse B, Casassus P |title=Churg-Strauss syndrome. Clinical study and long-term follow-up of 96 patients |journal=Medicine (Baltimore) |volume=78 |issue=1 |pages=26–37 |date=January 1999 |pmid=9990352 |doi= |url=}}</ref><ref name="pmid16614512">{{cite journal |vauthors=Oh MJ, Lee JY, Kwon NH, Choi DC |title=Churg-Strauss syndrome: the clinical features and long-term follow-up of 17 patients |journal=J. Korean Med. Sci. |volume=21 |issue=2 |pages=265–71 |date=April 2006 |pmid=16614512 |pmc=2734002 |doi=10.3346/jkms.2006.21.2.265 |url=}}</ref><ref name="pmid25500434">{{cite journal |vauthors=Greco A, Rizzo MI, De Virgilio A, Gallo A, Fusconi M, Ruoppolo G, Altissimi G, De Vincentiis M |title=Churg-Strauss syndrome |journal=Autoimmun Rev |volume=14 |issue=4 |pages=341–8 |date=April 2015 |pmid=25500434 |doi=10.1016/j.autrev.2014.12.004 |url=}}</ref>
-**Prodromal phase: Most common manifestations include allergic rhinitis and asthma.
+**'''Prodromal phase:''' Most common manifestations include [[Rhinitis|allergic rhinitis]] and [[asthma]].
-**Eosinophilic phase: This phase is characterized by peripheral eosinophilia and infiltration of eosinophils in multiple organs. Most commonly involved organs are lung and GI tract.
+**'''Eosinophilic phase:''' This phase is characterized by [[Eosinophilia|peripheral eosinophilia]] and infiltration of [[Eosinophil granulocyte|eosinophils]] in multiple organs. Most commonly involved organs are [[lung]] and [[Gastrointestinal tract|GI tract]].
-**Vasculitic phase: This phase is characterized by small and medium-sized vasculitis and inflammatory granuloma formation. Granulomas can be either vascular or extravascular. Commonly involved organs include lungs, kidneys, skin and peripheral nerves.
+**'''Vasculitic phase:''' This phase is characterized by small and medium-sized [[vasculitis]] and inflammatory granuloma formation. Granulomas can be either vascular or extravascular. Commonly involved organs include [[Lung|lungs]], [[Kidney|kidneys]], [[skin]], [[heart]], and [[Peripheral nervous system|peripheral nerves]].
 ===History===