Extensive mandibular radiolucency with minimal expansion
29-year-old female
§Chief complaint
Vague discomfort in the left lower jaw; lesion found on a routine radiograph
§Medical & dental history
- 01No basal cell carcinomas, no family history of naevoid basal cell carcinoma syndrome
- 02Otherwise healthy
- 03All teeth present and vital
- 04No previous surgery in the region
§Clinical examination
- 01Barely perceptible expansion of the left mandible despite a large radiographic lesion
- 02Mucosa intact; no discharge or tenderness
- 0334 to 38 all vital on electric pulp testing
- 04No paraesthesia of the lower lip; mouth opening normal
§ figuresFigures (4)
Fig. 1角化嚢胞性歯原性腫瘍の組織像
“Keratocystic odontogenic tumor” · Baldanders · CC BY-SA 3.0 · Wikimedia Commons
Fig. 2massive keratocystic odontogenic tumour (previously odontogenic keratocyst) with impacted wisdom teeth superficial to lesion
“Massive keratocystic odontogenic tumour” · Coronation Dental Specialty Group [1] · CC BY 3.0 · Wikimedia Commons
Verified open-access images only, reproduced for education under their stated licences · no AI-generated or illustrative artwork · Odontogenic Keratocyst figures pending faculty review.
§Differential diagnosis
§Final diagnosis
Odontogenic keratocyst of the left mandibular body and ramus
Growth along the marrow spaces with disproportionately little cortical expansion, vital teeth, and aspiration of thick keratinaceous material with low soluble protein points to OKC; parakeratinised lining with a palisaded basal layer confirms it.
§Investigations
- 01Aspiration — thick, cheesy, keratin-containing material; total soluble protein below 4 g/dL
- 02Pulp testing of all teeth in the quadrant — vital
- 03Skin and skeletal survey to exclude naevoid basal cell carcinoma syndrome — negative
- 04Incisional biopsy before definitive surgery
§Radiology
- 01OPG — well-defined multilocular radiolucency 55 mm extending from 34 to the ramus with a scalloped corticated margin
- 02CBCT — cortical thinning without ballooning, lingual perforation at two points, minimal root resorption
§Treatment plan
- 01Incisional biopsy to confirm diagnosis
- 02Enucleation with peripheral ostectomy and Carnoy's solution application
- 03Preserve the inferior alveolar nerve and the dentition where possible
- 04Long-term radiographic surveillance for at least 5 years
§Surgical procedure
- 01Wide buccal flap exposure, careful enucleation of the friable lining in fragments
- 02Peripheral ostectomy 1-2 mm with a round bur under copious irrigation
- 03Chemical fixation with modified Carnoy's solution for 3 minutes, nerve protected with gauze
- 04Closure over a resorbable haemostatic dressing
§Histopathology report
Cyst lined by uniformly thin parakeratinised stratified squamous epithelium, 5-8 cells thick, with a palisaded, polarised hyperchromatic basal layer and a corrugated luminal surface. Daughter cysts present in the wall. No dysplasia. Odontogenic keratocyst.
§Follow-up & outcome
- 01Annual OPG for 5 years, then biennially
- 0212 months — progressive bony infill, no lucency at the margins
- 0336 months — no recurrence, lip sensation normal
Outcome: No recurrence at 3 years with preserved nerve function and dentition.
§Discussion
- 01OKC recurrence rates range from about 3% after resection to over 25% after simple enucleation, driven by satellite cysts and a friable lining.
- 02Multiple OKCs, especially in a young patient, demand a search for naevoid basal cell carcinoma syndrome (PTCH1).
- 03Marsupialisation followed by delayed enucleation reduces lesion size and morbidity in very large cysts.
§Clinical pearls / learning points
- 01Little expansion with a large radiolucency is the classic OKC signature.
- 02Enucleation alone is not enough — add peripheral ostectomy or a chemical adjunct.
- 03Multiple keratocysts should trigger a syndrome work-up.
§Viva questions
What is the histological hallmark of an OKC?
Thin uniform parakeratinised lining with a palisaded hyperchromatic basal layer and corrugated surface keratin.
Why does OKC recur?
Friable lining that tears on removal, satellite/daughter cysts and epithelial islands in the wall, and intrinsic growth potential.
Name the syndrome associated with multiple OKCs.
Naevoid basal cell carcinoma (Gorlin-Goltz) syndrome, from PTCH1 mutation.
§MCQs
Q1Aspirate from an odontogenic keratocyst characteristically shows:
Q2The gene implicated in naevoid basal cell carcinoma syndrome is:
§ evidenceReferences & Evidence
Current Classification
WHO Classification of Head and Neck Tumours
5th Edition — Volume 9
WHO Classification of Tumours Editorial Board · 2022
The authoritative international classification of head and neck, odontogenic and salivary gland tumours. Current terminology on this site follows this edition.
Evidence summary
Highest level of evidence linked to this page: WHO / Official Classification.
- L1 · Classification — 3
- L3 · Systematic review — 1
- L4 · Research — 1
- L6 · Textbook — 3
1 linked source was published from 2024 onwards. Where guidance is limited or contested, rely on the higher-level sources above rather than this summary. Educational use only — not a substitute for clinical judgement.
Content last reviewed
September 2026
Evidence last reviewed
September 2026
Next scheduled review
September 2027
Review status
EVIDENCE REVIEWED
Search latest PubMed evidence
Last literature search: 7 September 2026
Current Classification
WHO Classification of Tumours Editorial Board. IARC / World Health Organization · 2022
The authoritative international classification of head and neck, odontogenic and salivary gland tumours. Current terminology on this site follows this edition.
Vered M, Wright JM. Head and neck pathology · 2022 · 16(1):63-75
Summary of odontogenic and maxillofacial bone tumour changes in the 5th edition WHO classification.
IARC / WHO. IARC · 2022
Continuously updated online edition of the WHO head and neck tumour classification.
Systematic Reviews & Meta-Analyses
Oginni FO, Alasseri N, Ogundana OM et al.. Oral and maxillofacial surgery · 2023 · 27(2):201-212
Evidence-based surgical algorithm derived from published outcomes for odontogenic keratocyst.
Radiology References
Dunfee BL, Sakai O, Pistey R et al.. Radiographics : a review publication of the Radiological Society of North America, Inc · 2006 · 26(6):1751-68
Radiologic-pathologic correlation of benign and malignant odontogenic lesions of the jaws.
Histopathology References
Barnes L. CRC Press · 2008
Detailed histopathological reference for head and neck diagnostic criteria.
Textbook References
Neville BW, Damm DD, Allen CM et al.. Elsevier · 2024
Standard reference textbook of oral and maxillofacial pathology used throughout this atlas.
Rajendran R, Sivapathasundharam B. Elsevier · 2020
Undergraduate and postgraduate oral pathology textbook widely used in BDS and FCPS curricula.
Additional sources cited on this page
- WHO Classification of Head and Neck Tumours, 5th edition, 2022.
- Pogrel MA. The keratocystic odontogenic tumour. Oral Maxillofac Surg Clin North Am.
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