Jeong Han-Sin, Son Young-Ik, Ko Young-Hyeh, Kim Sang Yoon
Department of Otorhinolaryngology--Head and Neck Surgery, Sungkyunkwan University School of Medicine, Samsung Medical Center, Korea.
J Laryngol Otol. 2006 Feb;120(2):154-7. doi: 10.1017/S0022215105003518. Epub 2005 Nov 25.
The sarcomatoid variant is a rare subtype of salivary duct carcinoma that comprises epithelial and sarcomatoid components. The authors present the first reported case of sarcomatoid salivary duct carcinoma occurring in the larynx, which was successfully treated by partial laryngectomy with ipsilateral neck dissection, with no evidence of recurrence after five years. Microscopic analysis revealed a composite epithelial and sarcomatoid tumour. The epithelial component was characterized by papillary proliferation of glandular and ductal structures lined with multilayered epithelial tumour cells. The sarcomatoid component was characterized by pleomorphic spindle cells with cytologic atypia, accompanied by small lymphoid cells, extensive proliferation of blood vessels and focal myxoid changes. To the best of our knowledge, only one case of sarcomatoid salivary duct carcinoma outside a major salivary gland has been reported previously in the literature, and this is the first report of sarcomatoid salivary duct carcinoma arising from the larynx.
肉瘤样变体是涎腺导管癌的一种罕见亚型,由上皮和肉瘤样成分组成。作者报告了首例发生于喉的肉瘤样涎腺导管癌病例,该病例通过部分喉切除术加同侧颈部清扫术成功治疗,五年后无复发迹象。显微镜分析显示为上皮和肉瘤样复合性肿瘤。上皮成分的特征是由多层上皮肿瘤细胞衬里的腺管结构呈乳头状增生。肉瘤样成分的特征是具有细胞学异型性的多形性梭形细胞,伴有小淋巴细胞、广泛的血管增生和局灶性黏液样改变。据我们所知,此前文献中仅报道过1例发生于大涎腺以外的肉瘤样涎腺导管癌,而这是首例源于喉的肉瘤样涎腺导管癌报告。