| Churg-Strauss syndrome |
| Classification and external resources |
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Micrograph showing an eosinophilic vasculitis consistent with Churg-Strauss syndrome. H&E stain.
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| ICD-10 |
M30.1 |
| ICD-9 |
446.4 |
| DiseasesDB |
2685 |
| MeSH |
D015267 |
Churg–Strauss syndrome (CSS, also known as eosinophilic granulomatosis with polyangiitis [EGPA] or allergic granulomatosis) is an autoimmune condition that causes inflammation of small and medium-sized blood vessels (vasculitis) in persons with a history of airway allergic hypersensitivity (atopy). It usually (but not always) manifests in three stages. The early (prodromal) stage is marked by airway inflammation; almost all patients experience asthma and/or allergic rhinitis; the second stage is characterized by abnormally high numbers of eosinophils (hypereosinophilia), which causes tissue damage, most commonly to the lungs and the digestive tract. The third and final stage consists of vasculitis, which can eventually lead to cell death and can be life-threatening.
The syndrome is rare, is not inherited, and is not contagious. It was first described by Jacob Churg (1910–2005) and Lotte Strauss (1913–1985) at Mount Sinai Hospital in New York City in 1951.[2][3] It was once considered a type of polyarteritis nodosa due to their similar morphologies.
Contents
- 1 Historical background
- 2 Signs and symptoms
- 2.1 Allergic stage
- 2.2 Eosinophilic stage
- 2.3 Vasculitic stage
- 3 Diagnosis
- 4 Risk stratification
- 5 Treatment
- 6 Famous patients
- 7 References
- 8 Bibliography
- 9 External links
Historical background
In 1951, pathologists Jacob Churg and Lotte Strauss reported "fever...hypereosinophilia, symptoms of cardiac failure, renal damage, and peripheral neuropathy, resulting from vascular embarrassment in various systems of organs" in a series of 13 patients with necrotizing vasculitis previously diagnosed as "periarteritis nodosa", accompanied by hypereosinophilia and severe asthma.[5] Churg and Strauss noted three features which distinguished their patients from other patients with periarteritis nodosa but without asthma: necrotizing vasculitis, tissue eosinophilia, and extravascular granuloma.[5] As a result, they proposed that these cases were evident of a different disease entity, which they referred to as "allergic granulomatosis and angiitis".[5]
Signs and symptoms
Churg–Strauss syndrome consists of three stages; however, not all patients develop all three stages or progress from one stage to the next in the same order,[6] and whereas some patients may develop severe or life-threatening complications such as gastrointestinal involvement and heart disease, some patients are only mildly affected, e.g. with skin lesions and nasal polyps.[7] Churg–Strauss syndrome is consequently considered a highly variable condition in terms of its presentation and its course.[6][7]
Allergic stage
The prodromal stage is characterized by allergy. Almost all patients experience asthma and/or allergic rhinitis, with more than 90% having a history of asthma that is either a new development, or the worsening of pre-existing asthma,[9] which may require systemic corticosteroid treatment.[6] On average, asthma develops from three to nine years before the other signs and symptoms.[6]
The allergic rhinitis may produce symptoms such as rhinorrhea and nasal obstruction, and the formation of nasal polyps that require surgical removal, often more than once. Sinusitis may also be present.
Eosinophilic stage
The second stage is characterized by an abnormally high level of eosinophils (a type of white blood cell) in the blood and tissues.[6] The symptoms of hypereosinophilia depend on which part of the body is affected, but most often it affects the lungs and digestive tract.[6] The signs and symptoms of hypereosinophilia may include weight loss, night sweats, asthma, cough, abdominal pain, and gastrointestinal bleeding.[6] Fever and malaise are often present.
The eosinophilic stage can last months or years, and its symptoms can disappear, only to return later.[6] Patients may experience the third stage simultaneously.[6]
Vasculitic stage
The third and final stage, and hallmark of Churg–Strauss syndrome, is inflammation of the blood vessels, and the consequent reduction of blood flow to various organs and tissues.[6] Local and systemic symptoms become more widespread and are compounded by new symptoms from the vasculitis.
Severe complications may arise. Blood clots may develop within the damaged arteries in severe cases, particularly in arteries of the abdominal region, which is followed by infarction and cell death, or slow atrophy. Many patients experience severe abdominal complaints; these are most often due to peritonitis and/or ulcerations and perforations of the gastrointestinal tract, but occasionally due to acalculous cholecystitis or granulomatous appendicitis.
The most serious complication of the vasculitic stage is heart disease, which is the cause of nearly one half of all deaths in patients with Churg–Strauss syndrome. Among heart disease-related deaths, the most usual cause is inflammation of the heart muscle caused by the high level of eosinophils, although some are deaths to inflammation of the arteries that supply blood to the heart or pericardial tamponade. Kidney complications have been reported as being less common.
Diagnosis
Diagnostic markers include eosinophil granulocytes and granulomas in affected tissue and anti-neutrophil cytoplasmic antibodies (ANCA) against neutrophil granulocytes. Differentiation from Wegener's granulomatosis is not difficult. Wegener's is closely associated with c-ANCA, while Churg-Strauss can be associated with elevations of p-ANCA.
The American College of Rheumatology 1990 criteria for diagnosis of Churg-Strauss Syndrome lists these criteria:
- Asthma
- Eosinophils greater than 10% of a differential white blood cell count
- Presence of mononeuropathy or polyneuropathy
- Non-fixed pulmonary infiltrates
- Presence of paranasal sinus abnormalities
- Histological evidence of extravascular eosinophils
For classification purposes, a patient shall be said to have Churg–Strauss syndrome (CSS) if at least four of these six criteria are positive. The presence of any four or more of the six criteria yields a sensitivity of 85% and a specificity of 99.7%.[12]
Risk stratification
The French Vasculitis Study Group has developed a five-point system ("five-factor score" or FFS) that predicts the risk of death in Churg–Strauss syndrome using clinical presentations. These five factors are:
- Reduced renal function (creatinine >1.58 mg/dl or 140 μmol/l)
- Proteinuria (>1 g/24h)
- Gastrointestinal hemorrhage, infarction, or pancreatitis
- Involvement of the central nervous system
- Cardiomyopathy
The lack of any of these factors indicates milder case, with a five-year mortality rate of 11.9%. The presence of one factor indicates severe disease, with a five-year mortality rate of 26%, and two or more indicate very severe disease: 46% five-year mortality rate.[13]
Treatment
Treatment for Churg–Strauss syndrome includes glucocorticoids (such as prednisolone) and other immunosuppressive drugs (such as azathioprine and cyclophosphamide). In many cases, the disease can be put into a type of chemical remission through drug therapy, but the disease is chronic and lifelong.
A systematic review conducted in 2007 indicated all patients should be treated with high-dose steroids, but in patients with an FFS of one or higher, cyclophosphamide pulse therapy should be commenced, with 12 pulses leading to fewer relapses than six. Remission can be maintained with a less toxic drug, such as azathioprine or methotrexate.[14]
Famous patients
The memoir Patient, by the musician Ben Watt, deals with Watt's mid-1990s experience with Churg–Strauss syndrome, and his recovery.[15] Watt's case was unusual in that it mainly affected his gastrointestinal tract, leaving his lungs largely unaffected; this unusual presentation contributed to a delay in proper diagnosis. His treatment required the removal of 10 ft of necrotized small intestine, leaving him on a permanently restricted diet.[15]
Umaru Musa Yar'Adua, the president of Nigeria from 2007–2010, reportedly suffered from Churg–Strauss syndrome and died in office of complications of the disease.[16]
DJ and author Charlie Gillett was diagnosed with Churg-Strauss in 2006; he died four years later.[17]
Japanese ski jumper Taku Takeuchi, who won the bronze medal in the team competition, suffers from the disease and competed at the Sochi Olympics less than a month after being released from hospital treatment.[18]
References
- ^ synd/2733 at Who Named It?
- ^ Churg J, Strauss L (1951). "Allergic granulomatosis, allergic angiitis, and periarteritis nodosa". Am. J. Pathol. 27 (2): 277–301. PMC 1937314. PMID 14819261.
- ^ a b c Hellmich B, Ehlers S, Csernok E, Gross WL (2003). "Update on the pathogenesis of Churg-Strauss syndrome". Clin. Exp. Rheumatol. 21 (6 Suppl 32): S69–77. PMID 14740430.
- ^ a b c d e f g h i j "Churg-Strauss syndrome - Symptoms". Mayo Clinic. Retrieved 30 June 2013.
- ^ a b Della Rossa A, Baldini C, Tavoni A, et al. (November 2002). "Churg-Strauss syndrome: clinical and serological features of 19 patients from a single Italian centre". Rheumatology (Oxford) 41 (11): 1286–94. doi:10.1093/rheumatology/41.11.1286. PMID 12422002.
- ^ Rich, Robert R.; Fleisher, Thomas A.; Shearer, William T.; Schroeder, Harry; Frew, Anthony J.; Weyand, Cornelia M. (2012). Clinical Immunology: Principles and Practice. Elsevier Health Sciences. p. 701. ISBN 9780723437109.
- ^ Masi AT, Hunder GG, Lie JT, et al. (August 1990). "The American College of Rheumatology 1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiitis)". Arthritis Rheum. 33 (8): 1094–100. doi:10.1002/art.1780330806. PMID 2202307.
- ^ 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. doi:10.1097/00005792-199601000-00003. PMID 8569467.
- ^ Bosch X, Guilabert A, Espinosa G, Mirapeix E (2007). "Treatment of antineutrophil cytoplasmic antibody associated vasculitis: a systematic review". JAMA 298 (6): 655–69. doi:10.1001/jama.298.6.655. PMID 17684188.
- ^ a b Whiting, Sam (10 April 1997). "Everything But the Final Song / Ben Watt lives to tell how he almost didn't". SFGate. Retrieved 30 June 2013.
- ^ "WikiLeaks: Yar’Adua Died Of Lung Cancer And Churg Strauss Syndrome, US Cables Confirm". Sahara Reporters. 2 September 2011. Retrieved 30 June 2013.
- ^ "Charlie Gillett - Obituary". The Daily Telegraph. 18 Mar 2010. Retrieved 30 June 2013.
- ^ http://www.thenational.ae/sport/olympics/japans-taku-takeuchi-overcame-illness-to-win-olympic-medal-i-thought-i-might-even-die
Bibliography
- Adu, Dwomoa; Emery, Paul; Madaio, Michael (2012). Rheumatology and the Kidney (2, illustrated ed.). Oxford University Press. ISBN 9780199579655.
- Churg, Andrew; Thurlbeck, William M. (1995). Pathology of the Lung (2, illustrated ed.). Thieme. ISBN 9780865775343.
- Rich, Robert R.; Fleisher, Thomas A.; Shearer, William T.; Schroeder, Harry; Frew, Anthony J.; Weyand, Cornelia M. (2012). Clinical Immunology: Principles and Practice. Elsevier Health Sciences. ISBN 9780723437109.
External links
- Churg-Strauss syndrome – MedLink Neurology Clinical Summary
- 13631492 at GPnotebook
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Vasculitis/arteritis: systemic vasculitis (M30–M31, 446)
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| Large vessel |
- Takayasu's arteritis
- Giant-cell arteritis
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| Medium vessel |
- Type III hypersensitivity
- Kawasaki disease
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| Small vessel |
| Pauci-immune |
- c-ANCA
- Granulomatosis with polyangiitis
- p-ANCA
- Churg-Strauss syndrome
- Microscopic polyangiitis
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| Type III hypersensitivity |
- Hypersensitivity vasculitis/Henoch–Schönlein purpura
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| Ungrouped |
- Acute hemorrhagic edema of infancy
- Cryoglobulinemic vasculitis
- Bullous small vessel vasculitis
- Cutaneous small-vessel vasculitis
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| Other |
- Goodpasture's syndrome
- Sneddon's syndrome
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anat (a:h/u/t/a/l,v:h/u/t/a/l)/phys/devp/cell/prot
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noco/syva/cong/lyvd/tumr, sysi/epon, injr
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proc, drug (C2s+n/3/4/5/7/8/9)
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