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Pathology of the Head and Neck

Pathology of the Head and Neck

Pathology of the Head and Neck

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Major <strong>and</strong> Minor Salivary Gl<strong>and</strong>s Chapter 5 155Fig. 5.48. Salivary duct carcinoma: invasive irregular ducts <strong>and</strong>cribriform structures strongly resemble ductal carcinoma <strong>of</strong> <strong>the</strong>breastFig. 5.49. Salivary duct carcinoma, mucin-rich variant. This iscomposed <strong>of</strong> a mixture <strong>of</strong> usual-type salivary duct carcinoma <strong>and</strong>lakes <strong>of</strong> mucinous adenocarcinomacarcinoma [142]. Some studies have shown SDCs to expressprostate specific antigen (PSA) or acid phosphatase[110, 120], but ano<strong>the</strong>r failed to confirm this [185] <strong>and</strong>similarly, only 1 out <strong>of</strong> 40 cases in a Mayo Clinic serieswas PSA-positive [115]. More recently cases <strong>of</strong> SDC showingpositive staining for HER-2/neu (c-erbB-2) protein onimmunohistochemistry have been published [202], <strong>and</strong><strong>the</strong> gene amplification has been demonstrated with FISHanalysis [204].Several rare morphological variants <strong>of</strong> SDC havebeen described, including cribriform [23], micropapillary[147], sarcomatoid [96], mucin-rich [190] <strong>and</strong> oncocytic(Figs. 5.49, 5.50) [184]. So-called low grade salivaryduct carcinoma [46] is probably a separate entity(see below).The differential diagnoses <strong>of</strong> SDC are high-grademucoepidermoid carcinoma, oncocytic carcinoma <strong>and</strong>some metastases. The diagnosis <strong>of</strong> mucoepidermoidcarcinoma requires <strong>the</strong> presence <strong>of</strong> squamous-like cells,mucus-producing cells <strong>and</strong> cells <strong>of</strong> intermediate type,<strong>and</strong> <strong>the</strong>re is no expression <strong>of</strong> <strong>and</strong>rogen receptors. Manysalivary oncocytic carcinomas probably demonstrateo<strong>the</strong>r types <strong>of</strong> malignancy (including SDC) with plentifuloncocytic cells, but a true oncocytic carcinoma lacksany features <strong>of</strong> SDC <strong>and</strong> is AR-negative. At present, nei<strong>the</strong>r<strong>of</strong> <strong>the</strong>se two differential diagnoses is clinically criticalsince <strong>the</strong> prognosis is similar. However, it is importantto identify metastatic carcinoma, particularly from<strong>the</strong> prostate or breast. In most cases, metastases will beobvious from clinical investigation <strong>and</strong> imaging studies,but <strong>the</strong> usual immunopr<strong>of</strong>ile <strong>of</strong> <strong>the</strong>se tumours is different:prostatic carcinomas tend to be AR+, ER−, PSA+,CK 7+; breast carcinoma tend to be usually AR−, <strong>of</strong>tenER +, PSA−, CK 7+; SDC is AR+, ER−, usually PSA−, <strong>and</strong>CK 7+.Fig. 5.50. Salivary duct carcinoma with oncocytic differentiation.The cells have ample granular cytoplasm with vesicular nuclei<strong>and</strong> prominent nucleoli. A clear distinction between oncocyticsalivary duct carcinoma <strong>and</strong> true oncocytic carcinoma may notbe possible, as <strong>the</strong>y may not be separate entitiesThe prognosis for SDC is poor, <strong>and</strong> most series haveshown that more than 70% <strong>of</strong> patients die <strong>of</strong> disease,usually within 3 years. Never<strong>the</strong>less, Grenko et al. [86]alluded to a minority (about 25–30%) who do well, but<strong>the</strong>ir study was unable to identify any particular features<strong>of</strong> this group. Amongst possible prognostic indicators,tumour size is probably important, with lesions

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