J Korean Assoc Oral Maxillofac Surg.  2010 Jun;36(3):172-176. 10.5125/jkaoms.2010.36.3.172.

Epithelial-mesenchymal transition in osteogenic sarcoma of the neck following oral squamous cell carcinoma

Affiliations
  • 1Department of Oral Pathology, Oral Cancer Research Institute, College of Dentistry, Yonsei University, Seoul, Korea.
  • 2Department of Oral and Maxillofacial Surgery, College of Dentistry, Yonsei University, Seoul, Korea. kimoms@yuhs.ac
  • 3Department of Advanced General Dentistry, College of Dentistry, Yonsei University, Seoul, Korea.

Abstract

Postirradiation extraosseous osteogenic sarcomas are uncommon in the head and neck, despite the extensive use of high-dose radiation. It has been described as de novo radiation-induced neoplasm. We present a 73-year-old male who had been treated by radiotherapy for gingival cancer 7 years earlier and later developed extraosseous osteogenic sarcomas (EOSs) of the neck. Microscopically, the neck mass was composed with mesenchymal malignant cells with cartilaginous and osteogenic differentiation. Immunohistochemical stain demonstrated strong positivity of tumor cells for Snail, the one of major epithelial-mesenchymal transition (EMT) inducer. The E-cadherin expression was scarce, showing inverse relationship to Snail expression. Compared with previous squamous cell carcinoma (SCC) of the gingiva, the present EOS sample revealed the remained epithelial cells on cytokeratin immunohistochemistry, suggesting the tumor arise from the cells of epithelial origin. We have also reviewed the previous 6 cases of head and neck EOSs carefully. The clinicopathologic features of the unusual lesion suggest that it is an incomplete EMT of precedent epithelial malignancy rather than de novo pathology.

Keyword

Squamous cell carcinoma (SCC); Extraosseous osteogenic sarcoma (EOS); Epithelial-mesenchymal transition (EMT); Snail; E-cadherin; Mouth neoplasms

MeSH Terms

Aged
Cadherins
Carcinoma, Squamous Cell
Composite Resins
Durapatite
Epithelial Cells
Epithelial-Mesenchymal Transition
Gingiva
Head
Humans
Immunohistochemistry
Keratins
Male
Mouth Neoplasms
Neck
Neoplasms, Radiation-Induced
Osteosarcoma
Snails
Cadherins
Composite Resins
Durapatite
Keratins

Figure

  • Fig. 1. A. Microscopically, primary gingiva lesion showed cords and nests of epithelial cells exhibiting aberrant accumulation of keratin.(arrow) B. Second primary tumor of buccal mucosa showed severe cellular abnormalities of hyperchromatism and pleomorphism. Scant production of keratin is notified. C-D. Microscopic feature revealed that lesion of the neck was composed of sarcomatous spindle cells with hypercellular cartilage and irregular osteoid.(D, aster-isk)(H&E staining, original magnification A, B, and D: x200, C: x100) (SCC: squamous cell carcinoma, EOS: extraosseous osteogenic sarcoma)

  • Fig. 2. Axial CT scan reveals a neck mass (asterisk) of approximately 3.0×3.0 cm in left level III. (CT: computed tomography)

  • Fig. 3. A. Immunohistochemical stain for previous SCC showed intense cytoplasmic staining for cytokeratin AE1/3, whole epithelial cell marker. B. Snail was detected in the nucleus of peripheral carcinoma cells. C. The cytoplasmic membranous expression of E-cadherin was occasional. D. The expression of N-cadherin could not be identified. E. The present EOS revealed the minimum positivity for cytokeratin Immunohistochemical staining. F. Sarcoma cells surrounding and whinin abnormal cartilage (asterisk) showed definitely strong Snail expression. G. E-cadherin disappeared through whole tumor samples. H. The scarce cytoplasmic membranous expression of N-cadherin was detected among the mesenchymal tumor cells. (Immunohistochemical stain, A and E: cytokeratin AE1/3, B and F: Snail, C and G: E-cadherin, D and H: N-cadherin, original magnification x200) (SCC: squamous cell carcinoma, EOS: extraosseous osteogenic sarcoma)


Reference

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