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3. Introduction
A cystic hygroma is a fluid-filled sac that
results from a blockage in the lymphatic
system.
It is most commonly located in the neck or
head area, but can be located anywhere in
the body.
It may be discovered in a fetes during a
pregnancy ultrasound, or it may be
apparent at birth as a soft bulge under the
skin. When it is identified on pregnancy
ultrasound, there is an increased risk for
miscarriage. In some cases, it is not
discovered until a person is older.
4. Symptoms
The signs and symptoms of a cystic hygroma can vary
depending on its size and location. Regardless of size, a
cystic hygroma can potentially cause functional
impairment of nearby structures or organs, as well as
disfigurement of affected areas This table lists symptoms
that people with this disease may have. For most
diseases, symptoms will vary from person to person.
People with the same disease may not have all the
symptoms listed. This information comes from a
database called the human phenotype ontology (HPO)
5. Causes
Both a baby’s genes and their environment in
the womb can cause problems with the way
their lymphatic system grows. This is how
cystic hygromas form. It may happen on its
own or with genetic conditions such as Turner,
Down, or Noonan syndromes.
When adults get a cystic hygroma, it can be
due to trauma or a past respiratory infection.
But it’s often not clear what caused the cyst. It
may even disappear during pregnancy.
6. Treatment
Treatment involves surgical removal of the
abnormal tissue whenever possible. However,
cystic hygromas can often invade other parts of
the neck, making this impossible.
Other treatments have been attempted with only
limited success, including:
Chemotherapy medications
Injection of sclerosing medications
Radiation therapy
Steroids
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