Takahira Masayuki, Nakamura Yasuhisa, Shimizu Shin-Ichi, Minato Hiroshi, Katori Nobutada, Kobayashi Hiroshi, Nakatani Yusuke, Sugiyama Kazuhisa
Department of Ophthalmology, Kanazawa University School of Medicine, Ishikawa, Japan.
Am J Ophthalmol. 2005 Aug;140(2):337-40. doi: 10.1016/j.ajo.2005.02.030.
To report a case of the lacrimal gland tumor diagnosed as carcinosarcoma (true mixed tumor) arising from a pleomorphic adenoma.
Interventional case report.
An 80-year-old Japanese woman was referred with a well-circumscribed tumor in the lacrimal fossa.
The tumor was excised, but the deepest portion remained because of heavy bleeding. Histopathologically, the tumor consisted of osteosarcomatous cells. No epithelial or myoepithelial component was identified by immunohistochemistry. Two months later, the tumor progressed further and was excised completely with lateral orbitotomy. The tumor consisted primarily of osteosarcomatous component but also had epithelial components including carcinoma and pleomorphic adenoma. Examinations did not detect local recurrence and metastasis at 10 post-operative months.
The tumor was diagnosed as true carcinosarcoma of the lacrimal gland arising from a pleomorphic adenoma. When lacrimal gland tumors containing sarcomatous components are encountered, carcinosarcoma should be included in the differential diagnosis.
报告一例泪腺肿瘤,诊断为源自多形性腺瘤的癌肉瘤(真性混合瘤)。
介入性病例报告。
一名80岁日本女性因泪腺窝出现边界清晰的肿瘤前来就诊。
肿瘤被切除,但因出血严重,最深层部分未切除。组织病理学检查显示,肿瘤由骨肉瘤细胞组成。免疫组化未发现上皮或肌上皮成分。两个月后,肿瘤进一步进展,通过外侧眶切开术将其完全切除。肿瘤主要由骨肉瘤成分组成,但也有上皮成分,包括癌和多形性腺瘤。术后10个月检查未发现局部复发和转移。
该肿瘤被诊断为源自多形性腺瘤的真性泪腺癌肉瘤。当遇到含有肉瘤成分的泪腺肿瘤时,鉴别诊断应包括癌肉瘤。