A.6. What is a cystic hygroma? What are the complications? What is the treatment?
Answer:
Cystic hygroma is a developmental malformation of the lymphatic system found most often in the posterior triangle of the neck and axilla of children. They are divided into suprahyoid and subhyoid masses. They are compressible masses that are most often found in infants younger than 1 year and can intermittently enlarge. Suprahyoid masses can be extremely difficult to manage because of the associated obstructive symptoms, feeding difficulties, and potential for infection, which can compromise airway patency. Surgical removal is the treatment of choice, but complete surgical removal of these masses is often impossible. Repeat debulking is sometimes the only treatment. The mortality of a prenatally diagnosed cystic hygroma remains high, due to other comorbidities and the risk of airway obstruction. Therefore, tracheal intubation at delivery while maintaining uninterrupted maternal-fetal circulation until the airway is secured (ex utero intrapartum treatment [EXIT] procedure) has been performed to prevent the fatal consequences of immediate postnatal airway obstruction. Other treatment modalities include radiofrequency ablation, CO2 laser therapy, and percutaneous sclerotherapy. Bleomycin, doxycycline, OK432, and tetracycline have been used as sclerosing agents with favorable results.
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