Temporal bone odontogenic carcinoma with dentinoid involving the facial nerve: case report with literature review

Abstract Background Odontogenic carcinoma with dentinoid (OCD) is a rare, poorly characterised tumour not yet included in the WHO classification of head and neck tumours. We report a rare case of OCD involving the temporal bone. Case presentation A 35-year-old male presented with longstanding facial nerve paralysis and progressive hearing loss. Radiological investigation revealed an erosive mass in the temporal bone. The tumour was successfully resected, and definitive histopathological analysis showed a picture of OCD. The patient received adjuvant radiotherapy and remains under close surveillance for recurrence. Conclusions This case broadens the anatomical spectrum of OCD and highlights the need to consider odontogenic tumours in the differential diagnosis of temporal bone lesions, despite their rarity at this site.

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Publication Details

Journal
The Egyptian Journal of Otolaryngology
Published
2026-10-18
DOI
https://doi.org/10.1186/s43163-026-01239-5
Primary Topic
Oral and Maxillofacial Pathology
Type
article
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article

Temporal bone odontogenic carcinoma with dentinoid involving the facial nerve: case report with literature review

Suad Al Jahdhami, Asem Ali Shalaby, Khalid Al Zaabi, Mohammed Al Washahi et al.
The Egyptian Journal of Otolaryngology
Oral and Maxillofacial Pathology
article

Temporal bone odontogenic carcinoma with dentinoid involving the facial nerve: case report with literature review

Suad Al Jahdhami, Asem Ali Shalaby, Khalid Al Zaabi, Mohammed Al Washahi, Eiman Al‐Ajmi, Nasser M. Altamami, Yousuf Al Saidi, Asim Qureshi, Amal Al Kaabi
article en

Abstract

Abstract Background Odontogenic carcinoma with dentinoid (OCD) is a rare, poorly characterised tumour not yet included in the WHO classification of head and neck tumours. We report a rare case of OCD involving the temporal bone. Case presentation A 35-year-old male presented with longstanding facial nerve paralysis and progressive hearing loss. Radiological investigation revealed an erosive mass in the temporal bone. The tumour was successfully resected, and definitive histopathological analysis showed a picture of OCD. The patient received adjuvant radiotherapy and remains under close surveillance for recurrence. Conclusions This case broadens the anatomical spectrum of OCD and highlights the need to consider odontogenic tumours in the differential diagnosis of temporal bone lesions, despite their rarity at this site.

The Egyptian Journal of OtolaryngologyVol. 42(1)
Openalex Percentile: Top 10%
Oral and Maxillofacial Pathology
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