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OMFS-0124PathologyintermediateMaxilla

Painless unilateral maxillary swelling in an adolescent

14-year-old female

Draft — educational study aid, pending faculty review.

§Chief complaint

Gradual enlargement of the left cheek over 3 years

§Medical & dental history

  • 01No cafe-au-lait macules, no endocrine abnormality
  • 02Menarche normal
  • 03No trauma or infection at the site

§Clinical examination

  • 01Diffuse, bony hard, non-tender enlargement of the left maxilla with facial asymmetry
  • 02Buccal expansion obliterating the sulcus; teeth displaced but vital
  • 03Overlying mucosa normal; no paraesthesia
  • 04No proptosis or visual disturbance

§ figuresFigures (5)

Fig. 1Medium power shot with the classic 'Chinese character' bone spicules.

Bone FibrousDysplasia LP CTR” · Sarahkayb · CC BY-SA 4.0 · Wikimedia Commons

Fig. 2Immature bony trabeculae in a fibrous stroma.

Bone FibrousDysplasia Jaw MP3 PA” · Sarahkayb · CC BY-SA 4.0 · Wikimedia Commons

Verified open-access images only, reproduced for education under their stated licences · no AI-generated or illustrative artwork · Fibrous Dysplasia figures pending faculty review.

§Differential diagnosis

Fibrous dysplasiaGround-glass, ill-defined blending margins, unilateral, adolescent
Ossifying fibromaWell-demarcated, encapsulated, displaces rather than blends
Paget diseaseElderly, bilateral, raised ALP, cotton-wool
OsteosarcomaRapid growth, pain, sunray spiculation

§Final diagnosis

Monostotic fibrous dysplasia of the left maxilla

The imaging signature is a ground-glass matrix with margins that blend imperceptibly into normal bone — the opposite of the sharply demarcated ossifying fibroma. Absence of cafe-au-lait macules and endocrinopathy excludes McCune-Albright syndrome.

§Investigations

  • 01CT — ground-glass matrix, expansion, cortical thinning, indistinct borders
  • 02Serum alkaline phosphatase mildly raised; calcium and phosphate normal
  • 03Incisional biopsy where the diagnosis is not radiologically certain
  • 04Endocrine screen and skeletal survey to exclude polyostotic disease

§Treatment plan

  • 01Observation until skeletal maturity where function and appearance permit
  • 02Conservative surgical recontouring for aesthetic or functional problems
  • 03Avoid radiotherapy — risk of sarcomatous transformation
  • 04Long-term clinical and radiographic review

§Surgical procedure

  • 01Recontouring osteoplasty via an intraoral vestibular approach after growth stabilised

§Histopathology report

Irregular, curvilinear trabeculae of woven bone (Chinese-letter pattern) without osteoblastic rimming, lying in a cellular fibrous stroma that merges with surrounding bone. Fibrous dysplasia.

§Follow-up & outcome

  • 01Facial symmetry improved after recontouring
  • 02Stable at 3 years with no regrowth
  • 03Advised on the small risk of malignant change

§Clinical pearls / learning points

  • 01Fibrous dysplasia tends to stabilise after skeletal maturity — timing surgery matters.
  • 02Never irradiate fibrous dysplasia.
  • 03The absence of osteoblastic rimming histologically helps separate it from ossifying fibroma.

§References

  • WHO Classification of Head and Neck Tumours, 5th ed. (2022).

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