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Lingual Leiomyosarcoma: A Histopathological Case Report.

Hristo Popov1, Lilyana Petkova1, George S Stoyanov2,1

  • 1General and Clinical Pathology/Forensic Medicine and Deontology, Medical University of Varna, Varna, BGR.

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|January 23, 2023
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Summary

This case report details a rare tongue tumor, pleomorphic leiomyosarcoma, in a 60-year-old male. Immunohistochemistry confirmed the smooth muscle origin despite initial suspicion of squamous cell carcinoma.

Keywords:
head and neck malignancyleiomyosarcomapathologyspindle shape tumortongue

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Area of Science:

  • Oncology
  • Pathology
  • Surgical Oncology

Background:

  • Leiomyosarcomas, rare smooth muscle neoplasms, typically occur in the reproductive system, GI tract, or subcutaneous tissues.
  • Their occurrence in the head and neck, particularly the tongue, is exceptionally rare due to limited smooth muscle presence.

Observation:

  • A 60-year-old male presented with a slow-growing, painless mass on the right lateral tongue margin.
  • Histopathology revealed pleomorphic spindle cells with bizarre nuclei, high mitotic activity, and fascicular growth pattern.
  • Initial differential diagnosis included sarcomatoid squamous cell carcinoma due to patient demographics and risk factors.

Findings:

  • Immunohistochemistry was crucial for definitive diagnosis, differentiating the tumor from epithelial malignancies.
  • The tumor was negative for pan-cytokeratin and desmin, focally positive for caldesmon, and positive for smooth muscle actin.
  • These markers confirmed the diagnosis of pleomorphic leiomyosarcoma of the tongue.

Implications:

  • This case highlights the importance of comprehensive histopathological and immunohistochemical evaluation for rare tongue malignancies.
  • Accurate diagnosis is vital for appropriate treatment planning and patient management of leiomyosarcoma.
  • Understanding the rare presentation of leiomyosarcoma in the oral cavity can aid clinicians in recognizing and diagnosing similar cases.