The normal distribution of body iron stores
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Hereditary hemochromatosis

Haemochromatosis, also spelled hemochromatosis, is a hereditary disease characterized by improper processing by the body of dietary iron which causes iron to accumulate in a number of body tissues, eventually causing organ dysfunction. It is the main iron overload disorder. more...

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Signs and symptoms

Haemochromatosis is notoriously protean, i.e. it presents with symptoms that are often initially attributed to other diseases.

Symptoms may include:

  • Malaise
  • Liver cirrhosis (with an increased risk of hepatocellular carcinoma, affecting up to a third of all homozygotes) - this is often preceded by a period of a painfully enlarged liver.
  • Insulin resistance (often patients have already been diagnosed with diabetes mellitus type 2)
  • Erectile dysfunction and hypogonadism
  • Congestive heart failure, arrhythmias or pericarditis
  • Arthritis of the hands (MCP and PIP joints), knee and shoulder joints
  • Dysfunction of certain endocrine organs:
    • Pancreatic gland
    • Adrenal gland (leading to adrenal insufficiency)
    • Parathyroid gland (leading to hypocalcaemia)
    • Pituitary gland
    • Testes or ovary (leading to hypogonadism)
  • A darkish colour to the skin (see pigmentation, hence its name Diabete bronze when it was first described by Armand Trousseau in 1865)
  • An increased susceptibility to certain infectious diseases caused by:
    • Vibrio vulnificus infections from eating seafood
    • Listeria monocytogenes
    • Yersinia enterocolica
    • Salmonella enteritidis (serotype Typhymurium)
    • Klebsiella pneumoniae
    • Escherichia coli
    • Rhizopus arrhizus
    • Mucor species

Males are usually diagnosed after their forties, and women about a decade later, owing to regular iron loss by menstruation (which ceases in menopause).

Diagnosis

Imaging features

Clinically the disease may be silent, but characteristic radiological features may point to the diagnosis. The increased iron stores in the organs involved, especially in the liver and pancreas, result in an increased attenuation at unenhanced CT and an decreased signal intensity at MR imaging. Haemochromatosis arthropathy includes degenerative osteoarthritis and chondrocalcinosis. The distribution of the arthropathy is distinctive, but not unique, frequently affecting the second and third metacarpophalangeal joints of the hand.

Chemistry

A first step is the measurement of ferritin, the tissue form of accumulated iron which is shed into the blood. Other markers of iron metabolism are the iron carrying protein transferrin (decreased), transferrin saturation (increased) and serum iron (increased). Genetic testing is performed if the biochemical markers are deranged.

Other blood tests routinely performed: blood count, renal function, liver enzymes, electrolytes, glucose (and/or an oral glucose tolerance test (OGTT)).

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Hereditary Hemochromatosis - patient education sheet
From American Family Physician, 3/1/02

What is hereditary hemochromatosis? What causes it?

Hereditary hemochromatosis is a health problem that is passed from parents to children. It is inherited by passing on the HFE gene. The HFE gene makes your body store too much iron. The extra iron builds up in your body. This is called "iron overload." Iron overload can damage tissues and organs.

Does anything else cause iron overload?

Yes, you could have iron overload that isn't caused by a hereditary problem. Iron overload can show up in people who have been taking iron pills for more than 10 years. People who have to get many blood transfusions might end up with iron overload. In addition, people with certain kinds of anemia or liver disease may also have iron overload.

What are some signs of hereditary hemochromatosis?

Most people with hereditary hemochromatosis show no signs of the illness until they are middle-aged. They might have only mild signs, like tiredness, or they might have arthritis or impotence. These signs can also be caused by something else. They might not mean that you have hereditary hemochromatosis.

The signs of hereditary hemochromatosis are different from person to person. Men are more likely to have signs than women. The signs you have depend on the amount of iron in your diet or if you are taking iron pills or drinking alcohol. Blood loss in menstruation and pregnancy can also be factors.

People who have a very high iron level may have skin with a bronze or gray color. Their liver may get bigger. Their lab tests may be abnormal. The liver may become scarred. They might get cirrhosis--permanent and extensive scarring in the liver. Other signs of hereditary hemochromatosis include diabetes, a weak heart, and problems with glands or joints.

How does my doctor find out if I have hereditary hemochromatosis?

Your doctor will ask you about certain signs, do a physical exam and look at the results of your blood tests. If your blood tests are not normal, your doctor might do a test to look for an HFE gene.

If you have signs of hereditary hemochromatosis, you might need to have a liver biopsy to see if your liver is damaged. For the biopsy, a small piece is taken from your liver and looked at under a microscope. If you have cirrhosis, you have a high risk for getting liver cancer. A few people need to have a liver transplant.

How is hereditary hemochromatosis treated?

You will probably have phlebotomy (say this: flee-bot-oh-me). This word means removal of blood. A pint of blood is taken out of your body once a week. It's just like donating blood.

It may take a few months to a few years of weekly phlebotomy to get the extra iron out of your body. Then you will have phlebotomy about four times a year to keep the iron from building up again. The goal of the treatment is to keep a normal level of iron in your blood.

If you have hereditary hemochromatosis, you can do some things to help:

* Don't take iron supplements, not even vitamins with iron in them.

* Don't eat very much red meat.

* Don't drink very much alcohol. You might give up all alcohol. Too much iron plus alcohol can make liver disease worse. Ask your doctor if you can drink alcohol and how much is OK for you to drink.

* Don't eat raw shellfish. Don't even touch raw shellfish, because you have an increased risk of bacterial infection.

What is the outlook for people with hereditary hemochromatosis?

With early diagnosis and treatment, nearly all the problems of hereditary hemochromatosis can be prevented. If the illness is diagnosed and treated before you get cirrhosis or diabetes, your life expectancy should be normal.

Who should be tested for hereditary hemochromatosis?

Everyone with a relative with hereditary hemochromatosis should have blood tests to see if they also have it. All people with medical conditions that could be caused by hereditary hemochromatosis should be checked for iron overload. Even if your lab results are normal, you might need to get blood tests again every few years if you have some of the signs of hereditary hemochromatosis or a relative with it.

Adult relatives of a person with hereditary hemochromatosis might consider having a special test to look for an abnormal HFE gene. This test would tell their doctor if they might also have hereditary hemochromatosis.

Your doctor should explain to you the benefits and risks of genetic testing, because you could have problems with your job or getting insurance if you have the HFE gene. That is why HFE gene testing usually is not recommended for children younger than 18 years of age.

COPYRIGHT 2002 American Academy of Family Physicians
COPYRIGHT 2002 Gale Group

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