Sporadic neurofibroma of facial nerve presenting as parotid gland tumor: a rare case report

Author:

Hassan Shko H1,Salih Karzan M1,Salih Abdulwahid M12,Qaradakhy Aras J134,Abdullah Ari M156,Saeed Yadgar A1,Muhialdeen Aso S1,Habibullah Imad J1,Dhahir Hardi M1,Kakamad Fahmi H127ORCID,Ahmed Masty K1

Affiliation:

1. Scientific Department, Smart Health Tower , Madam Mitterrand Street, Sulaymaniyah, Kurdistan 46001 , Iraq

2. Department of Surgery, College of Medicine, University of Sulaimani , Zanko Street, Sulaymaniyah, Kurdistan 46001 , Iraq

3. Department of Radiology , , Shorsh Street, Sulaymaniyah, Kurdistan 46001 , Iraq

4. Shorsh Teaching Hospital , , Shorsh Street, Sulaymaniyah, Kurdistan 46001 , Iraq

5. Department of Pathology , , Zanko Street, Sulaymaniyah, Kurdistan 46001 , Iraq

6. Sulaymaniyah Teaching Hospital , , Zanko Street, Sulaymaniyah, Kurdistan 46001 , Iraq

7. Kscien Organization , Hamdi Street, Azadi Mall, Sulaymaniyah, Kurdistan 46001 , Iraq

Abstract

Abstract Intraparotid gland neurofibroma is a rare benign tumor that arises from Schwann cells of the facial nerve within the parotid gland. This case report discusses a 41-year-old woman who experienced a painless preauricular swelling on her right side for over 5 years. Clinical examination and ultrasound revealed a well-defined mass in the parotid gland. The patient underwent total mass excision, resulting in transient facial nerve dysfunction but complete recovery. These tumors often manifest as solitary masses in the parotid region and may compress nearby structures, causing facial paralysis or numbness. Their diagnosis can be challenging due to similarities with other parotid gland tumors and possible associations with neurofibromatosis. Managing intraparotid tumors, including neurofibromas, involves a multidisciplinary approach with input from cytopathologists, radiologists, and surgeons.

Publisher

Oxford University Press (OUP)

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