Churg-Strauss syndrome history and symptoms: Difference between revisions

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{{Churg-Strauss syndrome}}
{{Churg-Strauss syndrome}}
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==Overview==
==Overview==


==History==
==History==
Obtaining a complete history is an important aspect in making a clinical diagnosis of Eosinophilic granulomatosis with polynagiitis. As it can help differentiate between the ANCA associated vasculitis and other possible causes that may mimic the disease. They include:
* Granulomatosis with polyangiitis
* Microscopic polyangiitis
* Idiopathic hyper-eosinophilic syndrome
* Drug induced


==Symptoms==
==Symptoms==
Symptoms can include:
The initial signs that are seen in patients presenting with Eosinophilic granulomatosis with polyangiitis are non-specific in nature. The following are signs and symptoms of Eosinophilic granulomatosis with polyangiitis:  
* [[Fever]]
 
* [[Weight loss]]
===Prodromal phase===
* [[Malaise]]
* Arthralgia
* [[Asthenia]]
* Myalgia
* Pyrexia
* Weight loss
* Asthma
* Nasal polyps
* Allergic rhinitis,
* Sinusitis
* Otitis media
* Sensorineural hearing loss
 
===Eosinophilic phase===
* Peripheral eosinophilia
* Pulmonary infiltrates
* Ground glass opacities
* Thickening of the bronchial wall
* Endomyocardial infiltrates
* Arrhythmia
* Pericarditis
* Abdominal pain
 
===Vascular phase===
* Pyrexia
* Weight loss
* Fatigue
* Multiplex mononeuritis
* Cerebral infarctions
* Rapid progressive glomerulonephritis
* Pauci-immune focal and segmental necrotizing glomerulonephritis
* Palpable purpura and nodules
* Maculopapular erythematous
* Livedo reticularis
* Petechiae
* Ecchymoses
 
 
 
 
 


==References==
==References==

Revision as of 17:10, 14 November 2016

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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

History

Obtaining a complete history is an important aspect in making a clinical diagnosis of Eosinophilic granulomatosis with polynagiitis. As it can help differentiate between the ANCA associated vasculitis and other possible causes that may mimic the disease. They include:

  • Granulomatosis with polyangiitis
  • Microscopic polyangiitis
  • Idiopathic hyper-eosinophilic syndrome
  • Drug induced

Symptoms

The initial signs that are seen in patients presenting with Eosinophilic granulomatosis with polyangiitis are non-specific in nature. The following are signs and symptoms of Eosinophilic granulomatosis with polyangiitis:

Prodromal phase

  • Arthralgia
  • Myalgia
  • Pyrexia
  • Weight loss
  • Asthma
  • Nasal polyps
  • Allergic rhinitis,
  • Sinusitis
  • Otitis media
  • Sensorineural hearing loss

Eosinophilic phase

  • Peripheral eosinophilia
  • Pulmonary infiltrates
  • Ground glass opacities
  • Thickening of the bronchial wall
  • Endomyocardial infiltrates
  • Arrhythmia
  • Pericarditis
  • Abdominal pain

Vascular phase

  • Pyrexia
  • Weight loss
  • Fatigue
  • Multiplex mononeuritis
  • Cerebral infarctions
  • Rapid progressive glomerulonephritis
  • Pauci-immune focal and segmental necrotizing glomerulonephritis
  • Palpable purpura and nodules
  • Maculopapular erythematous
  • Livedo reticularis
  • Petechiae
  • Ecchymoses




References

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