Journals / Clinical Dentistry and Research / 2016 / Cilt: 40 - Sayı: 2

MANDİBULADA GÖRÜLEN DEZMOPLASTİK FİBROMA: VAKA RAPORU

DESMOPLASTIC FIBROMA OF THE MANDIBLE: A CASE REPORT

Pages
73–78
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

This report describes a case of desmoplastic fibroma in a 20 year old female presenting as a firm, painless mass in the labial side of the left mandibular lateral incisor with a radiolucency of adjacent bone on radiographs.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Desmoplastic fibroma of bone is an uncommon myofibroblastic tumor characterized by local aggressive behavior that is associated with a high-recurrence rate.
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Key Findings & Data:The lesion most frequently occurs in the mandibular posterior area in children or young adults.
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Conclusion & Impact:This report describes a case of desmoplastic fibroma in a 20 year old female presenting as a firm, painless mass in the labial side of the left mandibular lateral incisor with a radiolucency of adjacent bone on radiographs.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Desmoplastic fibroma of bone is an uncommon myofibroblastic tumor characterized by local aggressive behavior that is associated with a high-recurrence rate. The lesion most frequently occurs in the mandibular posterior area in children or young adults. Radiographically, it appears as a multilocular or occasionally unilocular radiolucency with well-defined or ill-defined margins. The treatment of patients with fibromatosis consists of wide surgical excision. Radiation therapy sometimes has been used. This report describes a case of desmoplastic fibroma in a 20 year old female presenting as a firm, painless mass in the labial side of the left mandibular lateral incisor with a radiolucency of adjacent bone on radiographs.

Özet

Kemiğin dezmoplastik fibroması, yüksek rekürrens oranı ile ilişkili lokal agresif davranış ile karekterize nadir görülen bir miyofibroblastik tümördür. Radyografik olarak, iyi sınırlı veya sınırları belirsiz, multilokuler veya bazen unilokuler radyolusensi olarak izlenir. Tedavisi geniş cerrahi eksizyondur. Bazen radyasyon tedavisi de kullanılabilir. Bu raporda, 20 yaşında kadın hastada sol mandibular lateral kesici dişin labialinde sert, ağrısız bir şişlikle kendini gösteren ve ilgili kemikte radyolusensiye sebep olmuş bir dezmoplastik fibroma olgusu sunulmaktadır.

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Cite This Article

SÜMER, A. P., SUMER, M., ÇALIŞKAN, A., GÜNHAN, Ö. (2016). MANDİBULADA GÖRÜLEN DEZMOPLASTİK FİBROMA: VAKA RAPORU. Clinical Dentistry and Research, Cilt: 40 - Sayı: 2, 73–78. https://ajindex.com/articles/145900

References (11)

  1. Watzinger F, Turhani D, Wutzl A, Fock N, Sinko K, Sulzbacher I. Aggressive fibromatosis of the mandible: a case report. Int J Oral Maxillofac Surg 2005; 34: 211-213. Angela C. Chi. Bone Pathology. In: Neville BW, Damm DD, Allen CM, Bouquot JE. Editors. Oral and Maxillofacial pathology. St. Louis, Elsevier; 2009. p. 613-677
  2. Castellazzi G, Vanel D, Le Cesne A, Le Pechoux C, Caillet H, Perona F et al. Can the MRI signal of aggressive fibromatosis be used to predict its behavior? Eur J Radiol 2009; 69: 222-229.
  3. Seper L, Bürger H, Vormoor J, Joos U, Kleinheinz J. Aggressive fibromatosis involving the mandible-case report and review of the literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2005; 99: 30-38.
  4. Sharma A, Ngan BY, Sandor GK, Campisi P, Forte V. Pediatric aggressive fibromatosis of the head and neck: a 20-year retrospective review. J Pediatr Surg 2008; 43: 1596- 1604. Stoeckle E, Coindre JM, Longy M, Binh MB, Kantor G, Kind M et al. A critical analysis of treatment strategies in desmoid tumours: a review of a series of 106 cases. Eur J Surg Oncol 2009; 35: 129- 134. Wang W, Koirala U, Ma S, Liu G, Ding M, Hu X et al. Age-based treatment of aggressive fibromatosis in the head and neck region. J Oral Maxillofac Surg 2014; 72: 311-321.
  5. Pena S, Brickman T, StHilaire H, Jeyakumar A. Aggressive fibromatosis of the head and neck in the pediatric population. Int J Pediatr Otorhinolaryngol 2014; 78: 1-4.
  6. Kruse AI, Luebbers HT, Gratz KW, Obwegeser JA. Aggressive fibromatosis of the head and neck: a new classification based on a literature review over 40 years (1968-2008). Oral Maxillofac Surg 2010; 14: 227-232.
  7. Arslan E, Işık AF, Şanlı M, Tunçözgür B, Elbeyli L. Toraks travması sonrası gelişen fibromatozis: Olgu sunumu. Türk Göğüs Kalp Damar Cerr Derg 2013; 21: 216-218.
  8. Çeçen AD, Kibar Y, Süslü H, Tatarlın, Hiçdönmez T. Torakolomber Stabilizasyondan Sonra Gelişen Tekrarlayıcı Fibromatozis: Olgu Sunumu. Sinir Sistemi Cerrahisi Derg 2010; 3: 81-83.
  9. Said-Al-Naief N, Fernandes R, Louis P, Bell W, Siegal GP. Desmoplastic fibroma of the jaw: A case report and review of literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2006; 101: 82-94. de Bree E, Zoras O, Hunt JL, Takes RP, Suarez C, Mendenhall W et al. Desmoid tumors of the head and neck: a therapeutic challenge. Head Neck 2014; 36: 1517-1526.
  10. Hu T, Jing G, Lv K. Aggressive fibromatosis in the maxilla. Br J Oral Maxillofac Surg 2009; 47: 129-131.
  11. Tuncer N, Keskin A, Baykul T, Demiralp S. Fibromat