Volume 21, Issue 2 pp. 168-171

Leiomyosarcoma of the parotid gland: A case report and review of the literature

John Kang MD

Corresponding Author

John Kang MD

Department of Otolaryngological and Communicative Disorders, Long Island Jewish Medical Center, New Hyde Park, New York

Department of Otolaryngological and Communicative Disorders, Long Island Jewish Medical Center, New Hyde Park, New YorkSearch for more papers by this author
Jonathan A. Levinson MD

Jonathan A. Levinson MD

Department of Surgery, Albert Einstein College of Medicine, Long Island Jewish Medical Center, New Hyde Park, New York

Search for more papers by this author
Ibrahim F. Hitti MD

Ibrahim F. Hitti MD

Department of Pathology, North Shore University Hospital at Forest Hills, Forest Hills, New York

Search for more papers by this author

Abstract

Background

A primary leiomyosarcoma of the parotid gland has been reported only three times in the English literature. This type of tumor represents an extremely rare group of salivary gland neoplasm.

Methods

A 44 year old man was initially seen with a 5 cm right parotid mass which was resected with a total parotidectomy, preserving the facial nerve. The patient had no palpable cervical lymph nodes.

Results

The majority of the specimen was made up of a relatively well demarcated tumor 5 cm in diameter. The tumor was noted to contain moderate to poorly differentiated primary leiomyosarcoma of the parotid.

Conclusions

A primary leiomyosarcoma of the parotid gland is an extremely rare existing entity. A review of the literature reveals that primary leiomyosarcoma and other sarcomas of the major salivary glands may share similar histogenesis and biologic behavior with their soft tissue counterparts. © 1999 John Wiley & Sons, Inc. Head Neck 21: 168–171, 1999.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.