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Hypereosinophilic syndrome

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Title: Hypereosinophilic syndrome  
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Hypereosinophilic syndrome

Hypereosinophilic syndrome
Classification and external resources
ICD-10 D72.1 (ILDS D72.12)
ICD-9-CM 288.3
ICD-O 9964/3
OMIM 607685
DiseasesDB 34939
eMedicine article/202030 article/1051555 article/886861
MeSH D017681

The hypereosinophilic syndrome (HES) is a disease characterized by a persistently elevated eosinophil count (≥ 1500 eosinophils/mm³) in the blood for at least six months without any recognizable cause, with involvement of either the heart, nervous system, or bone marrow.[1]

HES is a diagnosis of exclusion, after clonal eosinophilia (such as leukemia) and reactive eosinophilia (in response to infection, autoimmune disease, atopy, hypoadrenalism, tropical eosinophilia, or cancer) have been ruled out.[2]

There are some associations with chronic eosinophilic leukemia[3] as it shows similar characteristics and genetic defects.[4]

If left untreated, HES is progressively fatal. It is treated with glucocorticoids such as prednisone.[2] The addition of the monoclonal antibody mepolizumab may reduce the dose of glucocorticoids.[5]


  • Classification 1
  • Signs and symptoms 2
  • Diagnosis 3
  • Treatment 4
  • Epidemiology 5
  • References 6
  • External links 7


In the heart, there are two forms of the hypereosinophilic syndrome, endomyocardial fibrosis and Loeffler's endocarditis.

  • Endomyocardial fibrosis (also known as Davies disease) is seen in tropical areas.[6][7]
  • Loeffler's endocarditis does not have any geographic predisposition.

Signs and symptoms

As HES affects many organs at the same time, symptoms may be numerous. Some possible symptoms a patient may present with include:


Numerous techniques are used to diagnose hypereosinophilic syndrome, of which the most important is blood testing. In HES, the eosinophil count is greater than 1.5 × 109/L.[4] On some smears the eosinophils may appear normal in appearance, but morphologic abnormalities, such as a lowering of granule numbers and size, can be observed.[4] Roughly 50% of patients with HES also have anaemia.[4]

Secondly, various imaging and diagnostic technological methods are utilised to detect defects to the heart and other organs, such as valvular dysfunction and arrhythmias by usage of echocardiography.[4] Chest radiographs may indicate pleural effusions and/or fibrosis,[4] and neurological tests such as CT scans can show strokes and increased cerebrospinal fluid pressure.[4]

A proportion of patients have a mutation involving the PDGFRA and FIP1L1 genes on the fourth chromosome, leading to a tyrosine kinase fusion protein. Testing for this mutation is now routine practice, as its presence indicates response to imatinib, a tyrosine kinase inhibitor.[8]


Treatment primarily consists of reducing eosinophil levels and preventing further damage to organs.[4]

  • Hypereosinophilic Syndrome research in UK
  • Hypereosinophilic Syndrome on
  • Hypereosinophilic Syndrome on eMedicine
  • Hypereosinophilic Syndrome (HES) on American Academy of Allergy, Asthma & Immunology
  • Hypereosinophilic syndrome on Mayo Clinic
  • DermNet systemic/hypereosinophilic

External links

  1. ^ Chusid MJ, Dale DC, West BC, Wolff SM (1975). "The hypereosinophilic syndrome: analysis of fourteen cases with review of the literature". Medicine (Baltimore) 54 (1): 1–27.  
  2. ^ a b Fazel R, Dhaliwal G, Saint S, Nallamothu BK (May 2009). "Clinical problem-solving. A red flag". N. Engl. J. Med. 360 (19): 2005–10.  
  3. ^ a b c d e f g h Longmore, Murray; Ian Wilkinson; Tom Turmezei; Chee Kay Cheung (2007). Oxford Handbook of Clinicial Medicine. Oxford. p. 316.  
  4. ^ a b c d e f g h i j k l m n o p Rothenberg, Marc E. "Treatment of Patients with the Hypereosinophilic Syndrome with Mepolizumab". Retrieved 2008-03-17.  Last updated: Updated: Oct 4, 2009 by Venkata Samavedi and Emmanuel C Besa
  5. ^ a b c Rothenberg ME, Klion AD, Roufosse FE, et al. (March 2008). "Treatment of patients with the hypereosinophilic syndrome with mepolizumab". N. Engl. J. Med. 358 (12): 1215–28.  
  6. ^ Cotran, Ramzi S.; Kumar, Vinay; Fausto, Nelson; Nelso Fausto; Robbins, Stanley L.; Abbas, Abul K. (2005). Robbins and Cotran pathologic basis of disease. St. Louis, Mo: Elsevier Saunders. p. 606.  
  7. ^ Smedema JP, Winckels SK, Snoep G, Vainer J, Bekkers SC, Crijns HJ (December 2004). "Tropical endomyocardial fibrosis (Davies' disease): case report demonstrating the role of magnetic resonance imaging" (PDF). Int J Cardiovasc Imaging 20 (6): 517–22.  
  8. ^ Cools J, DeAngelo DJ, Gotlib J, et al. (2003). "A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome". N. Engl. J. Med. 348 (13): 1201–14.  


Patients who lack chronic heart failure and those who respond well to Prednisone or a similar drug have a good prognosis.[4] However, the mortality rate rises in patients with anaemia, chromosomal abnormalities or a very high white blood cell count.[4]

HES is very rare, with only 50 cases being noted and followed up in the United States between 1971 and 1982,[4] corresponding roughly to a prevalence of 1 to 2 per million people. The disease is even more uncommon within the paediatric population.[4]


[5] If this becomes successful, it may be possible for corticosteroids to be eradicated and thus reduce the amount of side effects encountered.[5], may be treated with the monoclonal antibody Mepolizumab currently being developed to treat the disease.Churg-Strauss syndrome and asthma After promising results in drug trials (95% efficiency in reducing blood eosinophil count to acceptable levels) it is hoped that in the future hypereosinophilic syndrome, and diseases related to eosinophils such as [4] Follow-up care is vital for the survival of the patient, as such the patient should be checked for any signs of deterioration regularly.[4]

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