Case Report

Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report

Volume: 4 Number: 3 September 23, 2025
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Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report

Abstract

Sialolith is one of the most common pathologies of the salivary glands. Approximately 5–20% of all sialoliths occur in the parotid gland. This case report presents the diagnosis and treatment process of a rare parotid sialolith. A 71-year-old male patient presented to our clinic with a 6-month history of pain and swelling in the left cheek region. Intraoral examination revealed tenderness and pus drainage at the level of the Stensen’s duct. Panoramic radiograph showed a radiopaque mass corresponding to the duct’s course. Cone-beam computed tomography (CBCT) was used to evaluate the size, location, and relationship of the sialolith to surrounding tissues. The sialolith was surgically removed via a transoral approach under local anesthesia. A drain was placed to maintain salivary flow. The patient made a full recovery without complications. This case demonstrates that parotid sialolith can be successfully managed with accurate diagnostic imaging and appropriate surgical planning.

Keywords

Ethical Statement

This case report does not require ethics committee approval. Written informed consent was obtained from the patient.

References

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  6. 6. Kondo, N., et al., The landmark for removal of sialoliths using sialendoscopy alone in parotid gland sialolithiasis. Auris Nasus Larynx, 2018. 45(2): 306-310.
  7. 7. Neto, V.T., et al., Giant Sialolith with 20 Years of Evolution in the Submandibular Duct. Open J Stomatol, 2020. 10.6.: 115-120.
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Details

Primary Language

English

Subjects

Facial Plastic Surgery

Journal Section

Case Report

Early Pub Date

September 23, 2025

Publication Date

September 23, 2025

Submission Date

July 4, 2025

Acceptance Date

August 11, 2025

Published in Issue

Year 2025 Volume: 4 Number: 3

APA
Yılmaz, B. E., Gökkurt Yılmaz, B. N., & Erdem, S. (2025). Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report. EurAsian Journal of Oral and Maxillofacial Surgery, 4(3), 71-76. https://izlik.org/JA85BR73CT
AMA
1.Yılmaz BE, Gökkurt Yılmaz BN, Erdem S. Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report. EJOMS. 2025;4(3):71-76. https://izlik.org/JA85BR73CT
Chicago
Yılmaz, Birkan Eyüp, Büşra Nur Gökkurt Yılmaz, and Sule Erdem. 2025. “Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report”. EurAsian Journal of Oral and Maxillofacial Surgery 4 (3): 71-76. https://izlik.org/JA85BR73CT.
EndNote
Yılmaz BE, Gökkurt Yılmaz BN, Erdem S (September 1, 2025) Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report. EurAsian Journal of Oral and Maxillofacial Surgery 4 3 71–76.
IEEE
[1]B. E. Yılmaz, B. N. Gökkurt Yılmaz, and S. Erdem, “Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report”, EJOMS, vol. 4, no. 3, pp. 71–76, Sept. 2025, [Online]. Available: https://izlik.org/JA85BR73CT
ISNAD
Yılmaz, Birkan Eyüp - Gökkurt Yılmaz, Büşra Nur - Erdem, Sule. “Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report”. EurAsian Journal of Oral and Maxillofacial Surgery 4/3 (September 1, 2025): 71-76. https://izlik.org/JA85BR73CT.
JAMA
1.Yılmaz BE, Gökkurt Yılmaz BN, Erdem S. Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report. EJOMS. 2025;4:71–76.
MLA
Yılmaz, Birkan Eyüp, et al. “Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report”. EurAsian Journal of Oral and Maxillofacial Surgery, vol. 4, no. 3, Sept. 2025, pp. 71-76, https://izlik.org/JA85BR73CT.
Vancouver
1.Birkan Eyüp Yılmaz, Büşra Nur Gökkurt Yılmaz, Sule Erdem. Diagnosis and Minimally Invasive Management of a Rare Parotid Gland Sialolith: A Case Report. EJOMS [Internet]. 2025 Sep. 1;4(3):71-6. Available from: https://izlik.org/JA85BR73CT

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