Unusual features of oral sarcomatoid carcinoma: a case report

Authors

  • Felippe José Almeida Loureiro Department of Oral Medicine, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre - RS, Brazil. Federal University of Rio Grande do Sul, Porto Alegre - RS, Brazil. https://orcid.org/0000-0002-2428-1199
  • Larissa Gabriely Oliveira Cavalcanti Department of Oral Medicine, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre - RS, Brazil. Federal University of Rio Grande do Sul, Porto Alegre - RS, Brazil. https://orcid.org/0000-0001-6574-6653
  • Lauren Frenzel Schuch Department of Pathology and Diagnosis of Oral Medicine, Faculty of Dentistry, University of the Republic, Montevideo, Uruguay. https://orcid.org/0000-0002-0993-936X
  • Vinicius Coelho Carrard Department of Oral Medicine, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre - RS, Brazil. Federal University of Rio Grande do Sul, Porto Alegre - RS, Brazil. https://orcid.org/0000-0002-1624-0178
  • Luis Fernando da Rosa Rivero Department of Pathology, Faculty of Medicine, Federal University of Rio Grande do Sul, Porto Alegre - RS, Brazil. https://orcid.org/0000-0001-9352-4257
  • Manoela Domingues Martins Department of Oral Pathology, Faculty of Dentistry, Federal University of Rio Grande do Sul, Porto Alegre - RS, Brazil. https://orcid.org/0000-0001-8662-5965
  • Marco Antonio Trevizani Martins Department of Oral Medicine, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre - RS, Brazil. Federal University of Rio Grande do Sul, Porto Alegre - RS, Brazil. https://orcid.org/0000-0001-6073-1807

DOI:

https://doi.org/10.22491/2357-9730.138820

Keywords:

Sarcomatoid carcinoma, Head and neck cancer, Spindle cell carcinoma, case report

Abstract

Oral sarcomatoid carcinoma (OSC) is considered a rare variant of oral squamous cell carcinoma (OSCC). It is extremely aggressive, affecting mainly older men with risk habits. We report an atypical case of OSC, in a 40-year-old black female that presented an invasive ulceration covering the left hard palate to the ipsilateral buccal mucosa with tissue loss and buccosinusal communication, measuring about 10 x 8 cm. The patient didn’t refer any risk habits. After incisional biopsy, histopathological examination was suggestive for a spindle cell malignant neoplasm. Immunohistochemistry (IHC) revealed positivity for keratins (CK) 7,8/18 and p63 and negativity for calponin, S-100, α-SMA and SOX-10. The patient underwent 9 cycles of chemoterapy, but unfortunately, she died 3 months later. This is an atypical case of OSC, since it usually occurs in older male patients with risk habits. This tumor may lead pathologists to misdiagnosis and IHC is crucial for definitive diagnosis.

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Author Biography

Luis Fernando da Rosa Rivero, Department of Pathology, Faculty of Medicine, Federal University of Rio Grande do Sul, Porto Alegre - RS, Brazil.

Additional Files

Published

2025-10-02

How to Cite

1.
Almeida Loureiro FJ, Oliveira Cavalcanti LG, Frenzel Schuch L, Coelho Carrard V, da Rosa Rivero LF, Domingues Martins M, et al. Unusual features of oral sarcomatoid carcinoma: a case report. Clin Biomed Res [Internet]. 2025 Oct. 2 [cited 2026 Sep. 11];45:e138820 . Available from: https://seer.ufrgs.br/index.php/hcpa/article/view/138820

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