Sclerosing polycystic adenosis of the salivary gland

Definition

The is a rare neoplasm of the salivary gland, closely resembling fibrocystic disease of the breast. Demonstration of clonality indicates that this is a true neoplasm.

Epidemiology

It occurs from the second decade of life onwards, with a female predominance.

Clinical features

Most cases occur in major salivary glands, but rarely it may arise within minor salivary glands. The tumour grows slowly

Histopathology

The mass is well demarcated and partially encapsulated. There is a proliferation of microcysts, ducts and acini within a sclerotic stroma, with a lobular architecture. Strangulated tubules resemble sclerosing adenosis of the breast. The epithelial cells are variably apocrine, foamy, vacuolated or mucinous. There is a varying degree of cytological atypia. A continuous layer of myoepithelial cells is present around the glandular units. A focal lymphocytic infiltrate is common.

Immunohistochemistry

 

EMA

positive in luminal epithelial cells

 

BRST-2

positive in luminal epithelial cells

Oestrogen receptor

positive in luminal epithelial cells

Progesterone receptor

positive in luminal epithelial cells

c-erb2

negative in luminal epithelial cells

   

Differential diagnosis

Prognosis

About one third of cases recur, but metastasis and death have not been reported.

References

1 Cheuk W,Chan JK. Advances in salivary gland pathology. Histopathology 2007; 51:1-20

 

This page last revised 8.7.2007.

©SMUHT/PW Bishop