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Cystic Hygroma in Children

Macrocystic lymphatic malformation typically located in the neck and axilla, presenting in infancy and childhood.

Written by: Saygı Hospital Health Guide Editorial Board
Published:

This content is for general information; please consult your physician for diagnosis and treatment.

References (5)

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What is Cystic Hygroma in Children?

Cystic hygroma, also called macrocystic lymphatic malformation, is a benign lymphatic anomaly composed of one or several large fluid-filled cavities lined by lymphatic endothelium. It commonly appears in the cervical, axillary or thoracic regions during infancy or early childhood.

Most cases are diagnosed in the prenatal period or during the first two years of life. Lesions can grow rapidly during infections or trauma, leading to airway compression, dysphagia or facial deformity. Sudden enlargement may follow upper respiratory infection. Posterior cervical hygromas in fetuses are associated with chromosomal abnormalities such as Turner syndrome.

Diagnosis is based on physical examination, ultrasound and MRI. Management includes observation for small asymptomatic lesions, sclerotherapy with agents such as bleomycin, doxycycline or OK-432, and surgical resection for selected cases. Recurrence is common; therefore long-term multidisciplinary follow-up by pediatric surgery, otolaryngology and interventional radiology teams is essential.

Symptoms

Soft compressible neck or axillary mass
Rapid swelling after infection
Airway compression
Dysphagia
Facial asymmetry
Skin discoloration over the lesion
Bleeding into the lesion after trauma

Risk Factors

Congenital lymphatic malformation
Turner syndrome and other chromosomal anomalies
Family history of vascular malformation
Recent upper respiratory infection
Local trauma
Pregnancy with prenatal cystic hygroma
Syndromic associations such as Noonan

When to See a Doctor?

If you experience any of the following symptoms, seek medical attention promptly:

  • Soft growing neck mass in a child
  • Sudden swelling after infection
  • Difficulty breathing or feeding
  • Bluish skin discoloration with mass
  • Recurrence after previous treatment
  • Concern about facial deformity

Treatment Methods

01
Detailed ultrasound and MRI evaluation
02
Observation for small asymptomatic lesions
03
Sclerotherapy with bleomycin or OK-432
04
Surgical excision in selected cases
05
Airway management when compressing
06
Genetic counseling when indicated
07
Multidisciplinary long-term follow-up

Which Department to Visit?

You can visit our Çocuk Sağlığı ve Hastalıkları department for these complaints. Our specialist physicians will create the most suitable treatment plan for you.

Learn About Çocuk Sağlığı ve Hastalıkları Department

Let us help you

You can make an appointment with our specialists or contact us for your concerns.

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Health Disclaimer: The information on this page is prepared for general informational purposes only. It does not replace medical diagnosis and treatment. Please consult your physician for your complaints. Saygı Hospital does not accept responsibility for actions taken based on the information on this page.