Leiomyosarcoma of the parotid gland: A case report and review of the literature
โ Scribed by Kang, John (author);Levinson, Jonathan A. (author);Hitti, Ibrahim F. (author)
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 135 KB
- Volume
- 21
- Category
- Article
- ISSN
- 1043-3074
No coin nor oath required. For personal study only.
โฆ Synopsis
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.
๐ SIMILAR VOLUMES
Three fine-needle aspiration biopsies from 2 patients with parotid masses yielded large numbers of nontyrosine crystalloids. One patient proved to have a benign cyst that was resected because it did not subside following two fine-needle aspirates. In a second patient, the swelling shrank after a cou
We report a case of desmoplastic malignant melanoma metastatic to the parotid gland initially evaluated by fine-needle aspiration. The cytologic findings consisted of scattered spindle cells in a background of heterogeneous lymphoid cells. The spindle cells were scant and displayed mild cytologic at
Background: Localized amyloidosis in the head and neck is a rare and benign process. Methods: We present the first case report in the literature of localized amyloidosis of the parotid glands and also comprehensively review the literature regarding localized amyloidosis of the head and neck. Resul
We describe a case of a 65-year-old Caucasian woman found to have an enlarging mass of the left adrenal gland. Laboratory examination revealed the mass to be nonfunctional. The patient underwent an uneventful left adrenalectomy. Pathological examination revealed the mass to be a leiomyoma. These tum