Abstract
Oral neurofibromas, a subtype of neurofibromas, represent benign tumors encasing a peripheral nerve within the oral cavity. These growths are intricately linked to the genetic disorder neurofibromatosis, posing unique challenges in diagnosis and management. Oral neurofibromas typically manifest as slow-growing, painless nodules or masses within the oral cavity. Common sites include the tongue, gingiva, and the buccal mucosa. While these tumors are generally benign, they can cause discomfort, interfere with oral functions, and, in some cases, lead to bleeding or ulceration. Diagnosing oral neurofibromas involves a combination of clinical examination, medical history review, and, in some cases, imaging studies. This case report discusses the histological, immunohistochemical, and surgical characteristics of oral neurofibroma to raise knowledge and comprehension of these diseases. HOW TO CITE THIS ARTICLE: Siroraj P, Hepzibah R, Anandan S, et al. A Unique Finding in an Adolescent Male: A Case Report Navigating in Detail about Oral Neurofibroma. Int J Clin Pediatr Dent 2025;18(5):591-594.