Tumour-like lesions of the salivary glands are diseases which, in acco
rdance with the new WHO classification of salivary gland tumours, can
simulate a true tumour by swelling or induration of the salivary gland
tissue. An additional rare entity, only recently not described in the
new WHO classification, is,,sclerosing polycystic sialadenopathy'' (s
.p.s.) which, especially in younger patients, results in nodular, inco
mpletely encapsulated,tumour-like masses mainly of the parotid gland.
Histologically, it is comparable to fibrocystic mastopathy and is char
acterized by distinct hyalinized, centrally accentuated sclerosing col
lageneous tissue with inclusion of cystically ectatic ducts and focal
epithelial hyperplasia. In the hyperplastic ducts, transluminal bridge
s and cribriform patterns can develop, sometimes also apocrine secreti
on and eosinophilic globules. The s.p.s. must be distinguished mainly
from cystadenoma, mucoepidermoid carcinoma and also from dysgenetic cy
stic parotid gland. Based on four of our own observations the differen
tial diagnosis is analysed.