{Reference Type}: Case Reports
{Title}: Melanotic Neuroectodermal Tumour of Infancy - A Case Report and Review of Literature.
{Author}: Jakka S;Roy ID;Rangan M;Pandey S;Singh AK;
{Journal}: Ann Maxillofac Surg
{Volume}: 12
{Issue}: 1
{Year}: Jan-Jun 2022
暂无{DOI}: 10.4103/ams.ams_5_22
{Abstract}: <B>UNASSIGNED: </B>Melanotic neuroectodermal tumour of infancy (MNTI) is universally described as a rare, benign, pigmented lesion which most frequently involves the maxilla. Its origin is well established to be in the neural crest cells. Due to the high recurrence rate and aggressive behaviour mimicking malignancy, it poses a great challenge in their diagnosis, treatment planning, and prognosis.<BR><B>UNASSIGNED: </B>Two-year-old female with no known comorbidities was brought in with the chief complaint of a growing swelling in the upper lip region.<BR><B>UNASSIGNED: </B>She was taken up for resection of the tumour under general anaesthesia. The specimen was subjected to histological and immunological examination confirming the diagnosis of MNTI.<BR><B>UNASSIGNED: </B>The postoperative period was uneventful. After regular follow-up, the patient showed satisfactory healing with no signs of recurrence.<BR><B>UNASSIGNED: </B>Based on our experience, we feel that the diagnosis of MNTI is mainly clinical. Early conservative surgical excision and regular follow-up provide an excellent result with good prognosis.