Churg-Strauss syndrome overview: Difference between revisions
(→Causes) |
|||
| Line 24: | Line 24: | ||
==Natural History, Complications and Prognosis== | ==Natural History, Complications and Prognosis== | ||
[[Eosinophilic granulomatosis with polyangiitis]] develops through three phases, include [[Prodrome|prodromal]] phase, eosinophilic phase, vasculitic phase. Most complications result from the vasculitic phase. Most common complications include [[cardiomyopathy]], [[myocardial infarction]], [[Pericarditis|perimyocarditis]], rapidly progressive [[Renal insufficiency|renal failure]], [[Gastrointestinal bleeding|GI bleeding]], [[neuropathy]] and [[status asthmaticus]]. Prognosis of [[eosinophilic granulomatosis with polyangiitis]] is poor if left untreated. [[Prognosis]] is most likely dependent on stage at which the [[disease]] was diagnosed and organ involvement. The five-factor score assessment (FFS) is a good predictor of survival rate. It can be used to choose the appropriate treatment. | |||
==Diagnosis== | ==Diagnosis== | ||
Revision as of 19:30, 3 April 2018
|
Churg-Strauss syndrome Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Churg-Strauss syndrome overview On the Web |
|
American Roentgen Ray Society Images of Churg-Strauss syndrome overview |
|
Risk calculators and risk factors for Churg-Strauss syndrome overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Churg-Strauss syndrome is a medium and small vessel autoimmune vasculitis, leading to necrosis. It involves mainly the blood vessels of the lungs (it begins as a severe type of asthma), gastrointestinal system, and peripheral nerves, but also affects the heart, skin and kidneys. It is a rare disease that is non-heritable, non-transmissable and often mis-diagnosed.
Historical Perspective
Classification
Revised International Chapel Hill Consensus Conference 2012 on nomenclature of vasculitides, defines eosinophilic granulomatosis with polyangiitis (formerly known as Churg - Strauss syndrome) as an eosinophilic, granulomatous inflammatory disease affecting most commonly the conducting pulmonary airways, and leading to a necrosis of the small and/or medium sized vessels. Eosinophilic granulomatosis with polyangiitis is often synonymous with adult-onset asthma. According to revised CHCC 2012, eosinophilic granulomatosis with polyangiitis is considered as a variant of the ANCA - associated vasculitis.
Pathophysiology
Eosinophilic granulomatosis with polyangiitis is a medium and small vessel vasculitis, leading to necrosis. The pathogenesis of Eosinophilic granulomatosis with polyangiitis is not fully understood. Eosinophilic granulomatosis with polyangiitis occurs as a result of a complex interaction involving genetic and environmental factors that lead to an inflammatory response involving eosinophils, lymphocytes. Autoimmunity has an evident role in the presence of ANCA, hypergammaglobulinemia, elevated levels of immunoglobulin E, and rheumatic factor in the pathogenesis. HLA-DRB4 is correlated with increased risk of development of vascular manifestations of the churg-strauss syndrome. On microscopic pathology, eosinophilic infiltration, necrotizing granulomas vasculitis and necrosis of small and medium-sized arteries can be seen.
Causes
The etiology of eosinophilic granulomatosis with polyangiitis is not known. Various allergens, infections, vaccinations and drugs may be responsible for developing disease through an allergic or autoimmune response. Genetics may play a role includes, HLA -DRB4 and IL-10 gene polymorphisms are associated with the development of eosinophilic granulomatosis with polyangiitis.
Differentiating Churg-Strauss syndrome from Other Diseases
Epidemiology and Demographics
Risk Factors
Natural History, Complications and Prognosis
Eosinophilic granulomatosis with polyangiitis develops through three phases, include prodromal phase, eosinophilic phase, vasculitic phase. Most complications result from the vasculitic phase. Most common complications include cardiomyopathy, myocardial infarction, perimyocarditis, rapidly progressive renal failure, GI bleeding, neuropathy and status asthmaticus. Prognosis of eosinophilic granulomatosis with polyangiitis is poor if left untreated. Prognosis is most likely dependent on stage at which the disease was diagnosed and organ involvement. The five-factor score assessment (FFS) is a good predictor of survival rate. It can be used to choose the appropriate treatment.