Post-radiotherapy recurrence of conventional oral squamous cell carcinoma showing sarcomatoid components: an immunohistochemical study

Authors

  • Túlio Morandin Ferrisse Universidade Estadual de São Paulo, Faculdade de Odontologia de Araraquara, Departamento de Diagnóstico e Cirurgia, Medicina Oral https://orcid.org/0000-0002-3520-4690
  • Audrey Foster Lefort Rocha Universidade Estadual de São Paulo, Faculdade de Odontologia de Araraquara, Departamento de Diagnóstico e Cirurgia, Medicina Oral https://orcid.org/0000-0002-0361-7407
  • Maria Letícia de Almeida Lança Universidade Estadual de São Paulo, Faculdade de Odontologia de Araraquara, Departamento de Diagnóstico e Cirurgia, Medicina Oral https://orcid.org/0000-0001-5768-9281
  • Heitor Albergoni Silveira Universidade Estadual de São Paulo, Faculdade de Odontologia de Araraquara, Departamento de Diagnóstico e Cirurgia, Medicina Oral https://orcid.org/0000-0002-6724-3504
  • Luciana Yamamoto Almeida Universidade Estadual de São Paulo, Faculdade de Odontologia de Araraquara, Departamento de Diagnóstico e Cirurgia, Medicina Oral https://orcid.org/0000-0001-5403-4052
  • Andreia Bufalino Universidade Estadual de São Paulo, Faculdade de Odontologia de Araraquara, Departamento de Diagnóstico e Cirurgia, Medicina Oral https://orcid.org/0000-0002-6714-6253
  • Jorge Esquiche León Universidade de São Paulo, Faculdade de Odontologia de Riberão Preto, Departamento de Estomatologia, Saúde Coletiva e Odontologia Legal, Patologia Oral https://orcid.org/0000-0002-9668-5870

DOI:

https://doi.org/10.4322/acr.2020.219

Keywords:

Squamous cell carcinoma, Squamous Cell Carcinoma of Head and Neck, immunohistochemistry, radiotherapy

Abstract

Spindle cell squamous cell carcinoma (SpSCC) is a rare biphasic malignant neoplasm, uncommonly affecting the oral cavity. The SpSCC diagnosis is difficult, especially when it exhibits inconspicuous morphology, inadequate tissue sampling, or association with an exuberant inflammatory reaction. Post-radiotherapy recurrent SpSCC occurring at the same site of conventional SCC is a rare phenomenon. A 59-year-old man was complained of “painful injury on the tongue” with 20 days of duration. He reported smoking and alcohol consumption. Medical history revealed conventional SCC on the tongue treated with surgery and radiotherapy 10 years ago. Intraoral examination showed a polypoid lesion with ulcerated areas, measuring 3 cm in diameter, on the tongue and floor of the mouth, at the same site of previous conventional SCC. The microscopical analysis showed small foci of carcinomatous component admixed with an exuberant inflammatory reaction. Immunohistochemistry highlighted the sarcomatoid component. Both malignant components were positive for EMA, CD138, p40 (deltaNp63), p63, and p53. Moreover, CK AE1/AE3 evidenced the carcinomatous component, whereas vimentin stained the sarcomatoid component. The Ki-67 was >10%. The current case emphasizes the importance of immunohistochemistry in the differential diagnosis of SpSCC from mimics and documents a rare complication of Ionizing Radiation.

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References

Ferlay J, Soerjomataram I, Dikshit R, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):E359-86. http://dx.doi.org/10.1002/ijc.29210. PMid:25220842.

Leemans CR, Braakhuis BJ, Brakenhoff RH. The molecular biology of head and neck cancer. Nat Rev Cancer. 2011;11(1):9-22. http://dx.doi.org/10.1038/nrc2982. PMid:21160525.

Martel C, Ferlay J, Franceschi S, et al. Global burden of cancers attributable to infections in 2008: a review and synthetic analysis. Lancet Oncol. 2012;13(6):607-15. http://dx.doi.org/10.1016/S1470-2045(12)70137-7. PMid:22575588.

Shield KD, Ferlay J, Jemal A, et al. The global incidence of lip, oral cavity, and pharyngeal cancers by subsite in 2012. CA Cancer J Clin. 2017;67(1):51-64. http://dx.doi.org/10.3322/caac.21384. PMid:28076666.

Pereira MC, Oliveira DT, Landman G, Kowalski LP. Histologic subtypes of oral squamous cell carcinoma: prognostic relevance. J Can Dent Assoc. 2007;73(4):339-44. PMid:17484800.

Gupta R, Singh S, Hedau S, et al. Spindle cell carcinoma of head and neck: an immunohistochemical and molecular approach to its pathogenesis. J Clin Pathol. 2007;60(5):472-5. http://dx.doi.org/10.1136/jcp.2005.033589. PMid:16731596.

Oktay M, Kokenek-Unal TD, Ocal B, Saylam G, Korkmaz MH, Alper M. Spindle cell carcinoma of the tongue: a rare tumor in an unusual location. Patholog Res Int. 2011;2011:572381. http://dx.doi.org/10.4061/2011/572381. PMid:21403898.

Romañach MJ, Azevedo RS, Carlos R, de Almeida OP, Pires FR. Clinicopathological and immunohistochemical features of oral spindle cell carcinoma. J Oral Pathol Med. 2010;39(4):335-41. http://dx.doi.org/10.1111/j.1600-0714.2009.00843.x. PMid:20002980.

Al-Bayaty H, Balkaran RL. Spindle cell carcinoma of the mandible: clinicopathological and immunohistochemical characteristics. J Oral Biol Craniofac Res. 2016;6(2):160-3. http://dx.doi.org/10.1016/j.jobcr.2015.08.009. PMid:27195215.

Kinra P, Srinivas V, Sinha K, Dutta V. Post irradiation spindle cell carcinoma of tonsillar pillar. Case Rep Med. 2011;2011:325193. http://dx.doi.org/10.1155/2011/325193. PMid:22203850.

Parikh N, Desai N. Spindle cell carcinoma of the oral cavity: a case report of a rare entity and review of literature. J Acad Adv Dent Res. 2011;2(2):31-6. http://dx.doi.org/10.1177/2229411220110206.

Chuang R, Crowe DL. Understanding genetic progression of squamous cell carcinoma to spindle cell carcinoma in a mouse model of head and neck cancer. Int J Oncol. 2007;30(5):1279-87. http://dx.doi.org/10.3892/ijo.30.5.1279. PMid:17390032.

Brown JS, Shaw RJ, Bekiroglu F, Rogers SN. Systematic review of the current evidence in the use of postoperative radiotherapy for oral squamous cell carcinoma. Br J Oral Maxillofac Surg. 2012;50(6):481-9. http://dx.doi.org/10.1016/j.bjoms.2011.08.014. PMid:22196145.

Cahan WG, Woodard HQ, Higinbotham NL, Stewart FW, Coley BL. Sarcoma arising in irradiated bone; report of 11 cases. Cancer. 1948;1(1):3-29. http://dx.doi.org/10.1002/1097-0142(194805)1:1<3::AID-CNCR2820010103>3.0.CO;2-7. PMid:18867438.

Maghami EG, St-John M, Bhuta S, Abemayor E. Postirradiation sarcoma: a case report and current review. Am J Otolaryngol. 2005;26(1):71-4. http://dx.doi.org/10.1016/j.amjoto.2004.08.005. PMid:15635588.

Koshy M, Paulino AC, Mai WY, Teh BS. Radiation-induced osteosarcomas in the pediatric population. Int J Radiat Oncol Biol Phys. 2005;63(4):1169-74. http://dx.doi.org/10.1016/j.ijrobp.2005.04.008. PMid:16054775.

Plichta JK, Hughes K. Radiation-induced angiosarcoma after breast-cancer treatment. N Engl J Med. 2017;376(4):367. http://dx.doi.org/10.1056/NEJMicm1516482. PMid:28121510.

Murray EM, Werner D, Greeff EA, Taylor DA. Postradiation sarcomas: 20 cases and a literature review. Int J Radiat Oncol Biol Phys. 1999;45(4):951-61. http://dx.doi.org/10.1016/S0360-3016(99)00279-5. PMid:10571202.

Coleman CN. Secondary neoplasms in patients treated for cancer: etiology and perspective. Radiat Res. 1982;92(1):188-200. http://dx.doi.org/10.2307/3575854. PMid:7134383.

Huang SH, O’Sullivan B. Oral cancer: current role of radiotherapy and chemotherapy. Med Oral Patol Oral Cir Bucal. 2013;18(2):e233-40. http://dx.doi.org/10.4317/medoral.18772. PMid:23385513.

Barker HE, Paget JT, Khan AA, Harrington KJ. The tumour microenvironment after radiotherapy: mechanisms of resistance and recurrence. Nat Rev Cancer. 2015;15(7):409-25. http://dx.doi.org/10.1038/nrc3958. PMid:26105538.

Durante M, Bedford JS, Chen DJ, et al. From DNA damage to chromosome aberrations: joining the break. Mutat Res. 2013;756(1-2):5-13. http://dx.doi.org/10.1016/j.mrgentox.2013.05.014. PMid:23707699.

Fenech M. Cytokinesis-block micronucleus cytome assay. Nat Protoc. 2007;2(5):1084-104. http://dx.doi.org/10.1038/nprot.2007.77. PMid:17546000.

Fajardo LF. The pathology of ionizing radiation as defined by morphologic patterns. Acta Oncol. 2005;44(1):13-22. http://dx.doi.org/10.1080/02841860510007440. PMid:15848902.

Huang RY, Guilford P, Thiery JP. Early events in cell adhesion and polarity during epithelial-mesenchymal transition. J Cell Sci. 2012;125(Pt 19):4417-22. http://dx.doi.org/10.1242/jcs.099697. PMid:23165231.

Zidar N, Boštjančič E, Gale N, et al. Down-regulation of microRNAs of the miR-200 family and miR-205, and an altered expression of classic and desmosomal cadherins in spindle cell carcinoma of the head and neck--hallmark of epithelial-mesenchymal transition. Hum Pathol. 2011;42(4):482-8. http://dx.doi.org/10.1016/j.humpath.2010.07.020. PMid:21237487.

Takata T, Ito H, Ogawa I, Miyauchi M, Ijuhin N, Nikai H. Spindle cell squamous carcinoma of the oral region. An immunohistochemical and ultrastructural study on the histogenesis and differential diagnosis with a clinicopathological analysis of six cases. Virchows Arch A Pathol Anat Histopathol. 1991;419(3):177-82. http://dx.doi.org/10.1007/BF01626345. PMid:1718079.

Minami SB, Shinden S, Yamashita T. Spindle cell carcinoma of the palatine tonsil: report of a diagnostic pitfall and literature review. Am J Otolaryngol. 2008;29(2):123-5. http://dx.doi.org/10.1016/j.amjoto.2007.02.006. PMid:18314024.

Manickam A, Saha J, Das Jr, Basu SK. A recurrent case of spinlde cell variant of squamous cell carcinoma. International Journal of Clinical & Medical Imaging. 2016;3(2):1000427. http://dx.doi.org/10.4172/2376-0249.1000427.

Okuyama K, Fujita S, Yanamoto S, et al. Unusual recurrent tongue spindle cell carcinoma with marked anaplasia occurring at the site of glossectomy for a well-differentiated squamous cell carcinoma: A case report. Mol Clin Oncol. 2017;7(3):341-6. http://dx.doi.org/10.3892/mco.2017.1323. PMid:28781811.

Leventon GS, Evans HL. Sarcomatoid squamous cell carcinoma of the mucous membranes of the head and neck: a clinicopathologic study of 20 cases. Cancer. 1981;48(4):994-1003. http://dx.doi.org/10.1002/1097-0142(19810815)48:4<994::AID-CNCR2820480424>3.0.CO;2-M. PMid:7272943.

Su HH, Chu ST, Hou YY, Chang KP, Chen CJ. Spindle cell carcinoma of the oral cavity and oropharynx: factors affecting outcome. J Chin Med Assoc. 2006;69(10):478-83. http://dx.doi.org/10.1016/S1726-4901(09)70312-0. PMid:17098672.

Iqbal MS, Paleri V, Brown J, et al. Spindle cell carcinoma of the head and neck region: treatment and outcomes of 15 patients. Ecancermedicalscience. 2015;9:594. http://dx.doi.org/10.3332/ecancer.2015.594. PMid:26635898.

Ohba S, Yoshimura H, Matsuda S, Imamura Y, Sano K. Spindle cell carcinoma arising at the buccal mucosa: a case report and review of the literature. Cranio. 2015;33(1):42-5. http://dx.doi.org/10.1179/0886963413Z.00000000026. PMid:25547144.

Berthelet E, Shenouda G, Black MJ, Picariello M, Rochon L. Sarcomatoid carcinoma of the head and neck. Am J Surg. 1994;168(5):455-8. http://dx.doi.org/10.1016/S0002-9610(05)80098-4. PMid:7977972.

Olsen KD, Lewis JE, Suman VJ. Spindle cell carcinoma of the larynx and hypopharynx. Otolaryngol Head Neck Surg. 1997;116(1):47-52. http://dx.doi.org/10.1016/S0194-5998(97)70351-6. PMid:9018257.

Slootweg PJ, Roboll PJM, Müller H, Lubsen H. Spindle-cell carcinoma of the oral cavity and larynx. Immunohistochemical aspects. J Craniomaxillofac Surg. 1989;17(5):234-6. http://dx.doi.org/10.1016/S1010-5182(89)80075-7. PMid:2474578.

Anderson CE, Al-Nafussi A. Spindle cell lesions of the head and neck: an overview and diagnostic approach. Diagn Histopathol. 2009;15(5):264-72. http://dx.doi.org/10.1016/j.mpdhp.2009.02.009.

Lewis JS Jr, Ritter JH, El-Mofty S. Alternative epithelial markers in sarcomatoid carcinomas of the head and neck, lung, and bladder-p63, MOC-31, and TTF-1. Mod Pathol. 2005;18(11):1471-81. http://dx.doi.org/10.1038/modpathol.3800451. PMid:15976812.

Carbone A, Gloghini A, Rinaldo A, Devaney KO, Tubbs R, Ferlito A. True identity by immunohistochemistry and molecular morphology of undifferentiated malignancies of the head and neck. Head Neck. 2009;31(7):949-61. http://dx.doi.org/10.1002/hed.21080. PMid:19378322.

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Published

2021-01-04

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Section

Clinical Case Report and Review

How to Cite

Ferrisse, T. M. ., Rocha, A. F. L., Lança, M. L. de A. ., Silveira, H. A. ., Almeida, L. Y. ., Bufalino, A. ., & León, J. E. . (2021). Post-radiotherapy recurrence of conventional oral squamous cell carcinoma showing sarcomatoid components: an immunohistochemical study. Autopsy and Case Reports, 11, e2020219. https://doi.org/10.4322/acr.2020.219