Skip to main content

Hypereosinophilic syndrome

Hypereosinophilic syndrome



Overview

Hypereosinophilic syndrome is organ damage or dysfunction caused by an excess of disease-fighting white blood cells called eosinophils.

Hypereosinophilic syndrome (hy-per-ee-o-SIN-o-phil-ik) is rare. It can affect any tissues in the body. Common targets include the skin, lungs, digestive tract, heart and nervous system.

If a condition is found to cause hypereosinophilic syndrome, then treating the underlying condition also may lower eosinophil levels. Other treatments include medicines that reduce the number of eosinophils in the bloodstream.

Symptoms

Symptoms of hypereosinophilic syndrome (HES) vary depending on what organs are affected. Early symptoms of HES may include:

Fatigue.

Cough.

Shortness of breath.

Muscle pain.

Swelling in deep layers of the skin.

Rash.

Fever.

Causes

Eosinophils are important in fighting parasites and bacteria. They also regulate other immune system cells and proteins that cause allergic reactions.

HES occurs when high levels of these white blood cells last a long time. The cells themselves or their byproducts can move into organs, where they can cause damage or dysfunction.

Terms to know

You may hear the following terms regarding HES.

Eosinophilia is a higher than typical number of eosinophils circulating in the bloodstream.

Hypereosinophilia is a high number of eosinophils that lasts for an extended period, usually at least one month.

Hypereosinophilia syndrome is organ damage or destruction caused by long-term high eosinophils.

Types of hypereosinophilia

Persistent increases in these white blood cells may be caused by a number of factors. General categories of hypereosinophilia based on cause include the following:

Primary hypereosinophilia is caused by cancers of the bone marrow or blood that directly increase the production of eosinophils.

Secondary hypereosinophilia, also called reactive hypereosinophilia, is caused by conditions that typically activate white blood cells, such as:

Parasitic or bacterial infections.

Allergies.

Immune system disorders.

Long-lasting inflammatory diseases.

Drug reactions.

Familial hypereosinophilia is an inherited disorder.

Idiopathic hypereosinophilia has no cause that can be found. Most cases are idiopathic.

Risk factors

HES can affect anyone, but it occurs more often in men.

Diagnosis

A diagnosis of is HES is based on persistent high levels of eosinophils and evidence of organ damage. Diagnostic tests are used to determine what has caused an increase of eosinophils and whether any tissues have been affected.

Your healthcare professional will ask a number of questions about symptoms, family medical history, medicines and possible exposure to disease.

Tests to determine cause

Your healthcare professional orders tests to determine the cause of increased eosinophils. These may include:

Blood tests to detect autoimmune conditions, infections, or evidence of blood-related cancers.

Allergy tests to detect environmental or food allergies.

Stool tests to detect parasitic infections such as hookworm.

Genetic test to check for rare gene mutations that can cause HES.

Bone marrow samples to detect possible cancers or other diseases of the bone marrow.

Tests to assess organ damage

Other tests are used to find out whether organs have been affected by high eosinophils. These may include:

Blood tests to check liver and kidney function.

Imaging tests to study the appearance and function of organs.

Echocardiogram to check heart function.

Lung function tests to measure how well you breathe in and out.

Tissue samples of organs that check for the presence of eosinophils or evidence of tissue damage.

Treatment

Treatment goals are to reduce eosinophil levels, lessen symptoms and prevent further damage to organs.

If an underlying cause is found, treatment for that condition also begins.

Medicines

The first line of treatment is usually a corticosteroid to lower the number of eosinophils circulating in the bloodstream.

Other medicines may be used depending on the cause of increased eosinophils or the response to corticosteroid treatment. They include:

Hydroxyurea (Droxia, Hydrea, others).

Imatinib (Gleevec).

Mepolizumab (Nucala).

Vincristine PFS.

Because HES can increase your risk of blood clots, you also may be prescribed blood-thinning medications such as warfarin (Coumadin).

Type of Doctor Department : An allergist/immunologist

Comments

Post a Comment

Popular posts from this blog

Charge Syndrome

Overview CHARGE syndrome is a recognizable genetic syndrome with known pattern of features. It is an extremely complex syndrome, involving extensive medical and physical difficulties that differ from child to child. CHARGE syndrome is correlated with genetic mutation to CHD7 and the prevalence of CHARGE syndrome is 1:10,000-1:15,000 live births. Babies with CHARGE syndrome are often born with life-threatening birth defects. They spend many months in the hospital and undergo many surgeries and other treatments. Swallowing and breathing problems make life difficult even when they come home. Most have hearing two little girls sitting on a carpet, one girl has a trach and is biting her finger.loss, vision loss, and balance problems that delay their development and communication. Despite these seemingly insurmountable obstacles, children with CHARGE syndrome often far surpass their medical, physical, educational, and social expectations. One of the hidden features of CHARGE syndrome is the ...
7 comments
Read more

HMSN Type I

 HMSN Type I Overview Hereditary motor and sensory neuropathy type 1 (HMSN I), also known as Charcot-Marie-Tooth disease type 1 (CMT1), is a group of inherited neurological disorders affecting the peripheral nerves. It is characterized by progressive muscle weakness and wasting, primarily in the feet and legs, as well as sensory loss. HMSN I is the most common form of HMSN and is typically caused by a duplication on chromosome 17p11.2-p12, including the PMP22 gene.  Symptoms Numbness and tingling: Often starting in the feet and potentially extending to the hands, these sensations can mimic poor circulation.  Reduced ability to feel pain and temperature: This can lead to unnoticed injuries and complications.  Motor Symptoms: Muscle weakness and wasting: Primarily affecting the distal muscles (those farthest from the body's core), such as the feet and hands.  Foot deformities: High arches (pes cavus) and hammer toes are frequently observed.  Gait abnormalit...
Post a Comment
Read more

Sjogren's syndrome

Sjogren's syndrome Overview Sjogren's (SHOW-grins) syndrome is a disorder of your immune system identified by its two most common symptoms — dry eyes and a dry mouth. The condition often accompanies other immune system disorders, such as rheumatoid arthritis and lupus. In Sjogren's syndrome, the mucous membranes and moisture-secreting glands of your eyes and mouth are usually affected first — resulting in decreased tears and saliva. Although you can develop Sjogren's syndrome at any age, most people are older than 40 at the time of diagnosis. The condition is much more common in women. Treatment focuses on relieving symptoms. Symptoms The two main symptoms of Sjogren's syndrome are: Dry eyes . Your eyes might burn, itch or feel gritty — as if there's sand in them. Dry mouth. Your mouth might feel like it's full of cotton, making it difficult to swallow or speak. Some people with Sjogren's syndrome also have one or more of the following: Joint pain, swel...
Post a Comment
Read more