Congenital intralingual cysts of foregut origin are extremely rare. These cysts have the potential to compromise the fetal airway at the time of delivery. We present a case of a 37-week fetus with an intralingual cyst identified by antenatal ultrasound and subsequently further delineated by MRI. Information acquired from the imaging allowed for controlled delivery with necessary precautions to manage an impending airway obstruction. Excision of the cyst occurred at day 8 of life. We have reviewed the literature as it pertains to our case as well as the role of imaging in managing fetal oral cavity cysts.Mucormycosis is a rare and life threatening fungal infection in children that occurs in association with immunocompromised states. Very few case reports of rhino-orbital mucormycosis have been documented in pediatric age group and most of these have been fatal. We report a case of mucormycosis in a child with renal disease who was managed with lipid complex amphotericin B coupled with surgical debridement.Lobular capillary haemangioma, formerly pyogenic granuloma, has an unclear etiopathogenesis and rarely occurs in an intravascular location.A 9-year-male with a right retroauricular mass that was clinically mistaken for a typical dermoid but appeared unusually vascular at excision was finally diagnosed as an intravascular lobular capillary haemangioma arising in a haemangioma (composite haemangioma). The histolopathologic features of lobules of capillaries in a loose oedematous fibromyxoid stroma and ''glomerulations'' confirmed the diagnosis. At 2 years after excision, there is no recurrence and he is asymptomatic.