Cystic hygroma, a congenital malformation characterized by fluid-filled cysts typically found in the head and neck region, presents unique challenges in neonatal care. This report examines three distinct cases of neonates diagnosed with head and neck cystic hygroma. The cases highlight the diverse clinical presentations, diagnostic considerations, and therapeutic interventions employed in managing this condition. By exploring these cases, we aim to contribute to the understanding of cystic hygroma in neonates, fostering improved clinical awareness and decision-making for healthcare professionals involved in neonatal care.