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Case Reports
. 2012:2012:356271.
doi: 10.1155/2012/356271. Epub 2012 Mar 19.

Sialadenoma papilliferum: clinical misdiagnosis with a histological decree

Affiliations
Case Reports

Sialadenoma papilliferum: clinical misdiagnosis with a histological decree

A Anuradha et al. Case Rep Dent. 2012.

Abstract

Sialadenoma papilliferum is a rare salivary gland tumor clinically resembling papilloma originating probably from the excretory duct. It is characterized by a biphasic growth pattern of exophytic squamous component and endophytic glandular component. We report a rare case of sialadenoma papilliferum in the floor of the mouth with epithelial dysplasia with pertinent review of literature. The present case highlights the importance of keeping sialadenoma papilliferum as a differential diagnosis of exophytic papilliferous oral lesions and the need to explore the etiology and malignant potential of the tumor.

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Figures

Figure 1
Figure 1
Surface papillary projections lined by a parakeratotic, acanthotic stratified squamous epithelium at 40x.
Figure 2
Figure 2
Dysplastic features such as basal cell hyperplasia, nuclear and cellular pleomorphism, and nuclear hyperchromatism at 400x.
Figure 3
Figure 3
Mitotic figures under oil immersion 1000x.
Figure 4
Figure 4
Mucous salivary gland with extralobular dilated tortuous ducts at 40x.
Figure 5
Figure 5
Dilated tortuous ducts lined by luminal columnar cells and abluminal cuboidal cells at 400x.

References

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