Abstract

10Nov 2017 PSAMMOMATOID JUVENILE OSSIFYING FIBROMA OF MAXILLA WITH SECONDARY ANEURYSMAL BONE CYST: A CASE REPORT WITH REVIEW OF LITERATURE. Noha Shaban Abo El Yazeed and Usama Abd El Raouf El Dakrory. Assistant lecturer in Oral pathology department Ahram Canadian University, MD. Cairo University, Lecturer in Oral and maxillofacial surgery department Misr University for Science and Technology, PhD Cairo University.

Highlights

  • Very few cases occur in association with the secondary aneurysmal bone cyst (ABC) formation have been reported in the literature, we present here an intraoral case in maxilla with secondary ABC in a four years old girl

  • This was done after Benjamins in 1938 who reported a lesion of the frontal sinus, which he termed “osteoid fibroma with atypical calcification” that was histologically similar to Gogl’s cases

  • Histopathology:Tumor tissue formed of immature bony trabeculae rimmed by osteoblasts in some areas embedded in cellular fibrous stroma fig (4), and multinucleated osteoclast-like giant cells was seen with occasional normal mitotic figures

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Summary

Introduction

This was done after Benjamins in 1938 who reported a lesion of the frontal sinus, which he termed “osteoid fibroma with atypical calcification” that was histologically similar to Gogl’s cases. Clinically:Johnson et al reviewed 3000 fibro-osseous lesions and found that 112 met the criteria for the juvenile active ossifying fibroma (6). Maxillary PJOF presents clinically with proptosis, visual disturbances, blindness from compression of the optic nerves and orbit, disturbances in ocular mobility, recurrent headaches, and nasal obstruction.(7) Aggressive growth occurs in some but not all cases encroaching adjacent orbital, nasal, and cranial compartments, distorting the face, displacing orbital contents, and blocking normal sinus drainage to form mucoceles.

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