{"title":"A case report of mandibular aggressive fibromatosis in a pediatric patient: diagnostic challenges and surgical management","authors":"Jiangying Yang, Xudong Tian, Ke Zhou, Yadong Wu","doi":"10.1016/j.ijscr.2025.111286","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Aggressive fibromatosis (AF) of the mandible is a rare, locally invasive tumor with significant diagnostic and therapeutic challenges. The incidence of AF in the head and neck region is estimated at 2–4 cases per 10 million people annually, with mandibular involvement being even less common. Its infiltrative nature and high recurrence risk necessitate meticulous surgical planning and prolonged follow-up.</div></div><div><h3>Case presentation</h3><div>A 15-year-old male presented with progressive left mandibular swelling and pain initially misdiagnosed as acute pulpitis. Imaging revealed a large soft tissue mass (64 mm × 68 mm) surrounding the left mandible with local bone destruction. Histopathological examination confirmed the diagnosis of aggressive fibromatosis. The patient underwent en bloc resection of the affected mandibular body and partial ramus, with preservation of vital structures. Despite conservative resection with 1–1.5 cm surgical margins, the patient experienced recurrence at 14 months post-surgery and underwent subsequent expanded tumor excision with mandibular segmental resection and fibular reconstruction at another institution.</div></div><div><h3>Discussion</h3><div>This case highlights the importance of accurate diagnosis and appropriate surgical management of mandibular AF. While our initial conservative approach was driven by economic constraints, the eventual recurrence necessitated more extensive surgery, emphasizing the importance of adequate surgical margins for this aggressive lesion.</div></div><div><h3>Conclusion</h3><div>Mandibular AF requires a comprehensive diagnostic approach and careful surgical planning. Clear surgical margins are essential to minimize recurrence risk, even if reconstruction must be delayed due to economic constraints. Long-term multidisciplinary follow-up is critical in pediatric cases both for tumor surveillance and to address developmental needs.</div></div>","PeriodicalId":48113,"journal":{"name":"International Journal of Surgery Case Reports","volume":"130 ","pages":"Article 111286"},"PeriodicalIF":0.6000,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210261225004729","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction
Aggressive fibromatosis (AF) of the mandible is a rare, locally invasive tumor with significant diagnostic and therapeutic challenges. The incidence of AF in the head and neck region is estimated at 2–4 cases per 10 million people annually, with mandibular involvement being even less common. Its infiltrative nature and high recurrence risk necessitate meticulous surgical planning and prolonged follow-up.
Case presentation
A 15-year-old male presented with progressive left mandibular swelling and pain initially misdiagnosed as acute pulpitis. Imaging revealed a large soft tissue mass (64 mm × 68 mm) surrounding the left mandible with local bone destruction. Histopathological examination confirmed the diagnosis of aggressive fibromatosis. The patient underwent en bloc resection of the affected mandibular body and partial ramus, with preservation of vital structures. Despite conservative resection with 1–1.5 cm surgical margins, the patient experienced recurrence at 14 months post-surgery and underwent subsequent expanded tumor excision with mandibular segmental resection and fibular reconstruction at another institution.
Discussion
This case highlights the importance of accurate diagnosis and appropriate surgical management of mandibular AF. While our initial conservative approach was driven by economic constraints, the eventual recurrence necessitated more extensive surgery, emphasizing the importance of adequate surgical margins for this aggressive lesion.
Conclusion
Mandibular AF requires a comprehensive diagnostic approach and careful surgical planning. Clear surgical margins are essential to minimize recurrence risk, even if reconstruction must be delayed due to economic constraints. Long-term multidisciplinary follow-up is critical in pediatric cases both for tumor surveillance and to address developmental needs.