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The clinicopathological and immunocytochemical features of nine cases of salivary duct carcinoma are described. This relatively rare tumour, which only recently has been widely recognized as a separate entity, is highly maligant and caused the death in eight of the patients. The tumour cells are arranged in cribriform and solid growth patterns, where the solid tumour nests frequently have comedo necrosis, and a fibrous, often sclerotic, stroma is present. The infiltrating desmoplasmic component and the diffuse invasive growth into adjacent adipose parotid tissue have similarities to ductal breast carcinoma. Immunocytochemical investigationof salivary duct carcinoma showed constant overexpression of c‐erbB‐2 as detected by membrane accentuation, and high proliferative activity as detected by nuclear positivity for MIB 1 (Ki‐67). Changes in the expression of p53 and retinoblastoma gene product do not …