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

被引:1
作者
Kang, J [1 ]
Levinson, JA
Hitti, IF
机构
[1] Long Isl Jewish Med Ctr, Dept Otolaryngol & Communicat Disorders, New Hyde Park, NY 11042 USA
[2] Long Isl Jewish Med Ctr, Albert Einstein Coll Med, Dept Surg, New Hyde Park, NY 11042 USA
[3] N Shore Univ Hosp, Dept Pathol, Forest Hills, NY USA
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 1999年 / 21卷 / 02期
关键词
leiomyosarcoma; parotid; mesenchymal; malignant salivary gland tumors;
D O I
10.1002/(SICI)1097-0347(199903)21:2<168::AID-HED12>3.0.CO;2-1
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
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. (C) 1999 John Wiley & Sons, Inc.
引用
收藏
页码:168 / 171
页数:4
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