Evidence map›Paper›PMID 42507055›Full record

ArticleHead and neck pathology2026

Pleomorphic Adenoma of the Palate with Bizarre Ductal and Myoepithelial Cells: A Case Image.

Katsutoshi Hirose, Masato Nakaguro, Kohei Kawamura, Taisuke Mori, Satoru Toyosawa

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In one paragraph

Article in Head and neck pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Katsutoshi HiroseDepartment of Oral and Maxillofacial Pathology, University of Osaka Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan. hirose.katsutoshi.dent@osaka-u.ac.jp.ORCID http://orcid.org/0000-0003-4148-1106
Masato NakaguroDepartment of Pathology and Laboratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8560, Japan.
Kohei KawamuraDepartment of Oral and Maxillofacial Surgery, University of Osaka Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Taisuke MoriDepartment of Diagnostic Pathology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Satoru ToyosawaDepartment of Oral and Maxillofacial Pathology, University of Osaka Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPleomorphic adenomas (PAs), the most common salivary gland tumors, are comprised of ductal epithelial and myoepithelial cells within a stromal background. A rare subset of PAs exhibits bizarre cells and 12q amplification involving HMGA2 and MDM2; in reported cases, bizarre cells have been confined to the myoepithelial component. We report the first case of a PA with bizarre-cytological features in both the ductal and myoepithelial components. CASE PRESENTATION: A 75-year-old woman presented with a palatal mass. Histology revealed a well-circumscribed biphasic tumor with marked nuclear pleomorphism in both luminal ductal and non-luminal myoepithelial cells. Despite the alarming atypia, mitotic activity was low, and neither necrosis nor invasive growth was observed. Immunohistochemically, luminal bizarre cells exhibited ductal characteristics, whereas non-luminal bizarre cells exhibited myoepithelial characteristics. Tumor cells were negative for androgen receptor and HER2 and showed a p53 wild-type expression pattern. The Ki-67 labeling index was < 5%, and the bizarre cells rarely tested positive. Molecular analysis demonstrated amplification of HMGA2 and MDM2, whereas no other pathogenic variants related to salivary gland tumors were detected. Complete excision was performed; no evidence of recurrence or metastasis was observed after 10 months.

conclusionMarked cytological atypia of bizarre cells in PA, even when involving ductal cells, may not necessarily indicate malignancy. This case highlights the value of integrating clinicopathological and genetic findings to better define PAs with bizarre cells and prevent overdiagnosis of carcinoma based on atypia alone.

Indexed as

Adenoma, PleomorphicPalatal NeoplasmsSalivary Gland NeoplasmsAgedBiomarkers, TumorFemaleHMGA2 ProteinHumansProto-Oncogene Proteins c-mdm2Biomarkers, TumorHMGA2 ProteinProto-Oncogene Proteins c-mdm212qHMGA2MDM2Pleomorphic adenomaSalivary glands

Identifiers

PMID42507055
PMCPMC13407779

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