Volume 13, Issue 3 pp. 239-242
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Schwannoma of the submandibular gland

Dr. LCDR Dennis D. Diaz MC, USNR

Dr. LCDR Dennis D. Diaz MC, USNR

Department of Otolaryngology-Head and Neck Surgery, Naval Hospital, Portsmouth, Virginia

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Dr. CDR Kevin S. Kennedy MC, USNR

Dr. CDR Kevin S. Kennedy MC, USNR

Department of Otolaryngology-Head and Neck Surgery, Naval Hospital, Portsmouth, Virginia

Eastern Virginia Medical School, Norfolk, Virginia and the Department of Surgery, F. Edward Hebert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland

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Dr. CPTN Gregg S. Parker MC, USN

Corresponding Author

Dr. CPTN Gregg S. Parker MC, USN

Department of Otolaryngology-Head and Neck Surgery, Naval Hospital, Portsmouth, Virginia

Eastern Virginia Medical School, Norfolk, Virginia and the Department of Surgery, F. Edward Hebert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland

Department of Otolaryngology-Head and Neck Surgery, Naval Hospital, Portsmouth, VA 23708-5000Search for more papers by this author
Dr. LCDR Valerie J. White MC, USN

Dr. LCDR Valerie J. White MC, USN

Department of Pathology, Naval Hospital, Portsmouth, Virginia

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First published: May/June 1991
Citations: 27

Abstract

Neurilemmomas (schwannomas) are solitary neurogenic tumors that arise from cells of the neural sheath. They are slow growing and represent a proliferation of Schwann cells. Extracranial neurogenic tumors of the head and neck are uncommon, with benign tumors occurring with greater frequency than malignant tumors. These tumors often mimic primary or metastatic disease in the head and neck. Schwannoma of the salivary gland is a particularly rare form of an extracranial neurogenic tumor, with most presenting in the parotid gland originating from a peripheral branch of the facial nerve. An unusual case of neurilemmoma of the submandibular gland is presented, and the literature concerning this subject is reviewed. We believe this tumor originated in an autonomic nerve of the submandibular gland. The mass was discrete and well demonstrated on CT scan. Total excision of the gland resulted in complete resolution of symptoms with no cranial nerve deficits.

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