Case report of an early diagnosed ameloblastic fibroma

Authors

  • Maryam Jafari ,School of Dentistry, Ilam University of Medical Sciences, Ilam, Iran.
  • Mina Hamian ,Dental and Oral Research Center, Department of Oral & Maxillofacial Medicine, School of Dentistry, Qom University of Medical Sciences, Qom, Iran.
  • Parichehr Ghalayani ,Department of Oral & Maxillofacial Medicine, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Samira Hajisadeghi ,Dental and Oral Research Center, Department of Oral & Maxillofacial Medicine, School of Dentistry, Qom University of Medical Sciences, Qom, Iran.
Abstract:

Abstract Ameloblastic fibroma is a relatively rare benign odontogenic tumor with two neoplastic components both epithelial and ectomesenchymal. A 10-year-old girl was referred to a dentist for routine dental treatments for evaluation of the distance between mandibular right first permanent molar and mandibular right second deciduous molar and it was associated with an undesirable backward movement of erupted mandibular right first permanent molar and forward movement of mandibular right second deciduous molar. The lesion was enucleated and the material was sent for histopathologic examination. Microscopically, it was composed of neoplastic proliferation of odontogenic epithelium consisted of cords and islands in a cell-rich mesenchymal stroma, with histopathological diagnosis of ameloblastic fibroma. After 24 months of follow-up, no recurrence was observed and the mandibular right first molar was spontaneously aligned. Early diagnosis and proper management will prevent comprehensive orthodontic treatment.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Ameloblastic fibroma: a case report.

The clinical and histopathologic features of a case of ameloblastic fibroma in a 9-year-old boy has been presented along with a review of the literature. The tumor responded to conservative surgical treatment and there was no recurrence one year postoperatively. Analysis of the literature suggests that the tumor may have a higher potential for recurrence than is generally appreciated. In additi...

full text

[Maxillary ameloblastic fibroma: a case report].

Ameloblastic fibroma (AF) is a benign tumor, it is a true mixed tumor composed of neoplastic epithelium and mesenchymal. This tumor is rare, and it almost arises in the mandible. A 22-years old female patient referred AF in the maxillary was present. The tumor was asymptomatic, except the right facial bulge. The radiograph showed a well-circumscribed neoplasm with several low density cysts invo...

full text

Treatment of large ameloblastic fibroma: a case report.

Ameloblastic fibroma (AF) is an extremely rare true mixed benign tumor that can occur in either the mandible or the maxilla, but is most frequently found in the posterior region of the mandible. It usually occurs in the first two decades of life and is associated with tooth enclosure, causing a delay in eruption or altering the dental eruption sequence. AF is diagnosed on routine radiographic e...

full text

Ameloblastic Fibroma of Anterior Maxilla – a Case Report

Ameloblastic fibroma is a rare mixed odontogenic tumour. Its usual site of occurrence is the posterior mandible, with very few cases being reported from the maxilla. The true nature of the lesion hamartomatous or neoplastic – is still a point of debate. Here, we report a case of ameloblastic fibroma in the anterior maxilla.

full text

Peripheral Ameloblastic Fibroma: Report of a Rare Case

Ameloblastic fibroma is a rare mixed odontogenic tumor mostly occurring in the posterior region of the mandible. The peripheral variant is very rare and to the best of our knowledge, only three cases have been reported in the English literature. In this report, we describe a case of peripheral ameloblastic fibroma in a 54-year-old woman with two years of follow-up.

full text

Recurrent Ameloblastic Fibroma: Report of a Rare Case

Ameloblastic fibroma (AF) is an uncommon mixed neoplasm of odontogenic origin frequently seen in the second decade of life. It mainly presents as an intrabony lesion but can even occur peripherally. Histologically, our case showed hypercellular areas, an uncommon feature seen in typical AF. Whether this benign lesion is treated by mode of enucleation and curettage or by extensive surgery is sti...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 4  issue None

pages  44- 49

publication date 2015-09

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023