Hosal A Sefik, Fan Chunyang, Barnes Leon, Myers Eugene N
Department of Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Otolaryngol Head Neck Surg. 2003 Dec;129(6):720-5. doi: 10.1016/S0194-59980301386-X.
Salivary duct carcinoma (SDC) is a highly malignant tumor that is histologically similar to ductal carcinoma of the breast. This article presents the clinicopathologic features of 15 patients with SDC arising in the salivary glands. The majority of patients were male and aged 65 years or older. The tumor was most often located in the parotid gland. Pain, facial palsy, and presence of calcification in the CT scan were diagnostic features suggestive of SDC. Histologically, 27% of the tumors arose from pre-existing pleomorphic adenoma. Perineural and lymphatic invasion were common findings. There was an extensive cervical lymph node involvement (73%). Distant metastasis was the most common cause of failure. Although SDC exhibits an unpredictable clinical course, total parotidectomy with neck dissection and adjunctive radiation therapy appear to be appropriate for local and regional control of this aggressive neoplasm.
涎腺导管癌(SDC)是一种高度恶性的肿瘤,在组织学上与乳腺导管癌相似。本文介绍了15例发生于涎腺的涎腺导管癌患者的临床病理特征。大多数患者为男性,年龄在65岁及以上。肿瘤最常位于腮腺。疼痛、面神经麻痹以及CT扫描中出现钙化是提示涎腺导管癌的诊断特征。组织学上,27%的肿瘤起源于先前存在的多形性腺瘤。神经周围和淋巴管浸润是常见表现。广泛的颈部淋巴结受累(73%)。远处转移是最常见的失败原因。尽管涎腺导管癌的临床病程不可预测,但全腮腺切除加颈部清扫及辅助放疗似乎适用于对这种侵袭性肿瘤的局部和区域控制。