A cystic hygroma is a mass that commonly occurs in the head and neck area. It is a birth defect.
Alternative NamesLymphangioma
Causes, incidence, and risk factorsA cystic hygroma occurs as the baby grows in the womb. It forms from pieces of material that carry fluid and white blood cells. Such material is called embryonic lymphatic tissue. After birth, a cystic hygroma usually looks like a soft bulge under the skin. The cyst may not be recognized at birth. It typically grows as the child does, and sometimes is not noticed until the child is older.
Sometimes, a cystic hygroma is seen when the baby is still in the womb using a pregnancy ultrasound. This can mean that the baby has a chromosomal problem or other birth defects.
SymptomsA common symptom is a neck mass found at birth, or discovered later in an infant after an upper respiratory tract infection.
Signs and testsThe following tests may be done:
If the cystic hygroma is detected during a pregnancy ultrasound, other ultrasound tests or amniocentesis may be recommended.
TreatmentTreatment involves complete removal of the abnormal tissue whenever possible. However, cystic hygromas can often invade other neck structures, making this impossible.
Other treatments have been attempted with only limited success. These include:
The outlook is good if surgery can totally remove the abnormal tissue. In cases where complete removal is not possible, the cystic hygroma commonly returns.
The outcome may also depend on what other chromosomal abnormalities or birth defects, if any, are present.
ComplicationsComplications may include:
If you notice a lump in your neck or your child's neck, call your doctor.
ReferencesCamitta BM. Abnormalities of lymphatic vessels. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 18th ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 489.
Richards DS. Ultrasound for pregnancy dating, growth, and the diagnosis of fetal malformations. In: Gabbe SG, Niebyl JR, Simpson JL, eds. Obstetrics: Normal and Problem Pregnancies. 5th ed. Philadelphia, Pa: Elsevier Churchill Livingstone; 2007:chap 9.
38555
Cystic hygroma is caused by a developmental defect in the lymphatic system, leading to the formation of fluid-filled sacs or cysts, typically in the neck or head region. This condition often arises during fetal development when lymphatic vessels fail to form properly. While the exact reasons for this abnormality are not fully understood, it may be associated with genetic factors or chromosomal abnormalities. Cystic hygromas can be detected through prenatal imaging techniques such as ultrasound.
The CPT code for the excision of a congenital cystic hygroma with dissection of deep neurovascular structures is typically 21555. This code is used for the excision of a tumor or cyst in the neck or face region, which includes the necessary dissection of surrounding neurovascular structures. However, it is always advisable to consult the most recent CPT coding guidelines or a coding specialist to ensure accuracy and compliance.
Normally diagnosed between 9 and 16 weeks' gestation.
A cystic foci, or cystic focus, is when an ultrasound identifies a finding that is cystic-like. It mean there's a tiny collection of fluid wherever the cystic focus was found.
What is cystic fibrosis? Cystic fibrosis is a life threatening disease.
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Is a carrier of cystic fibrosis
Yes, girls can get cystic fibrosis.
cystic fibrosis foundation
No. Cystic fibrosis is a genetic disease.
No. Cystic fibrosis is a genetic disease.