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Leiomyosarcoma of the parotid gland: A case report and review of the literature
Author(s) -
Kang John,
Levinson Jonathan A.,
Hitti Ibrahim F.
Publication year - 1999
Publication title -
head and neck
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.012
H-Index - 127
eISSN - 1097-0347
pISSN - 1043-3074
DOI - 10.1002/(sici)1097-0347(199903)21:2<168::aid-hed12>3.0.co;2-1
Subject(s) - parotid gland , leiomyosarcoma , histogenesis , salivary gland , medicine , facial nerve , parotidectomy , head and neck , pathology , soft tissue , tongue , anatomy , immunohistochemistry , surgery
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.

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