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May 7, 2026Libyan International Medical University Journal0 citationsOpen Access

Mangement of Large Conventional Ameloblastoma with Follicular and Plexiform Patterns in a Very Young Child: Case Report and Literature Review

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MAM.F. AdeyemiOAOsamede Desmond AgbonifoOAOluwatosin Alarape Adegboye

Key Points

  • To report a rare case of giant ameloblastoma in a very young child and discuss management strategies.
  • Case report of a 3-year-old female with an 18-month history of mandibular swelling.
  • Clinical examination revealed a large intraoral tumor with radiographic findings suggesting an odontogenic cystic lesion.
  • The tumor was surgically excised with hemi-mandibulectomy and temporomandibular joint disarticulation.
  • The histology confirmed a conventional ameloblastoma with mixed follicular and plexiform patterns.
  • The patient remained clinically stable during follow-up, suggesting successful management.
  • Highlights the importance of early presentation to prevent recurrence.

Abstract

Ameloblastoma is a rare benign odontogenic tumor with locally aggressive behavior, typically affecting adults. Pediatric cases, especially giant mandibular ameloblastoma with mixed follicular and plexiform histological type in very young children, are uncommon and pose unique diagnostic and management challenges. Our PubMed search did not yield any previously reported case from Nigeria. A 3-year-old female child presented with an 18-month history of progressive right mandibular swelling causing noticeable facial asymmetry. Clinical examination revealed a large, non-tender intraoral tumor with ulceration and tooth mobility. Radiographic imaging showed a heterogeneous, expansive mandibular lesion containing an unerupted tooth, consistent with an odontogenic cystic lesion. The tumor was radically excised through combined intraoral and extraoral approaches, including hemi-mandibulectomy and temporomandibular joint disarticulation. Histology revealed a conventional ameloblastoma with mixed follicular and plexiform pattern. The patient has remained clinically stable on follow-up. This case highlights the importance of early presentation, recognizing histopathological diversity in ameloblastoma, and underscores the need for aggressive surgical management with adequate margins in pediatric cases to prevent recurrence.

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Cite This Study

Adeyemi et al. (2026) studied this question.

synapsesocial.com/papers/69fbef86164b5133a91a37cbhttps://doi.org/10.1055/s-0046-1820432
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