How is LCH diagnosed?

Donate

Langerhans Cell Histiocytosis (LCH)How is LCH diagnosed?
The diagnosis of LCH is usually made by performing a biopsy of an affected part of the body. A biopsy is the removal of a small piece of tissue while a patient is under an anaesthetic. This piece of tissue is then examined under a microscope.

Doctors will be carrying out a number of further tests. These tests are done to see how LCH affects that part of the body and if any other systems are involved (multi-system disease). This information helps the medical team to decide on the best treatment for your child.

Some of the following tests may be carried out on your child:
• Blood tests these are done to check how many of the of different types of blood cells there are and to assess how well the liver and kidneys are working

• Urine test to evaluate how concentrated/dilute the urine is

• X-ray pictures of the chest and of the bones (also known as a skeletal survey).

• Ultrasound Scan – sound waves are used to build up a picture of the inside of the body. A clear gel is spread over the skin and a microphone is passed over the body. The sound waves bounce off the organs inside the body and are picked up by the microphone. A computer turns the sound waves into pictures.

• CT Scan – A CT (Computerised Tomography) scan takes a number of x-ray pictures of the body from different angles and uses a computer to convert them into cross-sectional x-ray pictures or ‘slices’ of the body. Depending on how big a part of the body is being scanned this can take between a few seconds and a few minutes. CT scans are painless, but small children may need to be sedated or anaesthetised (‘put to sleep as for an operation’) to ensure they remain still while the scan takes place.

• MRI Scan – Magnetic Resonance Imaging (MRI) Scan uses magnetic and radio waves to take pictures of the body. It is painless, but usually takes longer than a CT scan and is quite noisy. As it is important to keep very still, small children are normally sedated or given an anaesthetic.

• Biopsy – the removal of a small piece of tissue from an organ or part of the body for microscopic examination. Most often the biopsy is done of affected bone or skin but biopsies may also need to be carried out on the liver, lung or bone marrow.

• Water Deprivation Test – if doctors suspect there is a hormone problem known as diabetes insipidus, your child may need to undergo a water deprivation test. This is a test to measure how much urine is made and how concentrated it becomes when no water is given to a patient for a certain amount of time (also called fluid privation test) to complete all of these tests can take between a few days and a couple of weeks and may involve a stay in hospital.

Please be advised that all the information you read here is not a replacement for the advice you will get from your consultant and their team.

LCH is divided into two main groups – single system and multi-system

Single system disease
When LCH is described as a ‘single system’ disease, it means that it is only affecting one system in the body – for example, skin, bone or an organ. The majority (>70%) of patients have single system disease. If the LCH is only present in one place in that particular system, it is called single site and if in more than one place, it is called multi-site or multi-focal disease. Therefore a child with several affected bones, but no disease elsewhere, is considered to have ‘single system, multi-focal’ disease.

Multi-system disease
When LCH is found in more than one ‘system’, for example, in both the skin and bone, it is described as ‘multi-system’ disease. Children with ‘multisystem’ disease affecting the liver, spleen or bone marrow, are considered to have a more serious form of LCH. This is then described as multi-system disease with ‘risk organ’ involvement and may require more intensive treatment.

This classification helps doctors to decide what treatment is required and for how long it should be given.

Please be advised that all the information you read here is not a replacement for the advice you will get from your consultant and their team.

Help ensure that we can continue to bring you this vital informational material, make a donation today

HistioUK

Your support is vital to ensure that we can continue to deliver our Research and Information Programmes. Thank you.

Make a donation