Poorly Differentiated Chordoma: Case Review

Author:

Kochergina N. V.1ORCID,Boulytcheva I. V.1ORCID,Prokhorov S. N.1ORCID,Bludov A. B.1ORCID,Fеdorova A. V.1ORCID,Spirina O. G.1ORCID,Shсhipakhina Ya. A.1ORCID

Affiliation:

1. N.N. Blokhin National Medical Research Center of Oncology

Abstract

Purpose: Demonstrate a clinical case of poorly differentiated chordoma, confirmed using a wide range of research methods.Material and methods: A 63-year-old female patient with poorly differentiated chordoma who underwent immunohistochemical examination, MRI, CT and scintigraphy.Results: An immunohistochemical study confirmed the morphological affiliation of the tumor, supplemented by the data of imaging methods.Conclusion: The poorly differentiated type of chordoma has a specific immunohistochemical picture, however, differential diagnosis based on imaging methods is currently a difficult task.

Publisher

Non-profit partnership Society of Interventional Oncoradiologists

Reference19 articles.

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2. McMaster ML, Goldstein AM, Bromley CM, et al. Chordoma: incidence and survival patterns in the United States, 1973-1995. Cancer Causes Control. 2001;12:1-11. DOI: 10.1023/a:1008947301735.

3. Wold LE, Laws ER Jr. Cranial chordomas in children and young adults. J Neurosurg. 1983;59:1043-7. DOI: 10.3171/jns.1983.59.6.1043.

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