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Sanakoeva A.V.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Samarin A.E.

Kommunarka Moscow Multidi-Field Clinical Center

Konopleva E.I.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Tarakanova A.V.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Sidorov I.V.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Druy A.E.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology;
Institute of Medical Cell Technologies

Karachunsky A.I.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Surgical treatment of intracerebral metastases of Ewing sarcoma in children. Case report and review

Authors:

Sanakoeva A.V., Samarin A.E., Konopleva E.I., Tarakanova A.V., Sidorov I.V., Druy A.E., Karachunsky A.I.

More about the authors

Journal: Burdenko's Journal of Neurosurgery. 2025;89(2): 92‑96

DOI: 10.17116/neiro20258902192

Read: 1259 times

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Table of contents

SURGICAL TREATMENT OF INTRACEREBRAL METASTASES OF EWING SARCOMA IN CHILDREN. CASE REPORT AND REVIEW
SURGICAL TREATMENT OF INTRACEREBRAL METASTASES OF EWING SARCOMA IN CHILDREN. CASE REPORT AND REVIEW

To cite this article:

Sanakoeva AV, Samarin AE, Konopleva EI, Tarakanova AV, Sidorov IV, Druy AE, Karachunsky AI. Surgical treatment of intracerebral metastases of Ewing sarcoma in children. Case report and review. Burdenko's Journal of Neurosurgery. 2025;89(2):92‑96. (In Russ., In Engl.)
https://doi.org/10.17116/neiro20258902192

Подписка 2025 Журнал «Вопросы нейрохирургии» имени Н.Н. Бурденко (Burdenko's Journal of Neurosurgery)
 
МСФ на ЯМ
Использование инфографики авторами научных работ
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Abstract:

BACKGROUND

Metastatic brain lesions following Ewing sarcoma of bones and soft tissues in children are extremely rare and have unfavorable prognosis. There are few publications devoted to this issue. Survival rates after craniotomy are extremely low.

The authors describe a patient with metastatic form of Ewing sarcoma and two intracerebral (supra- and infratentorial) metastases. Total resection with subsequent radio- and chemotherapy were followed by stable remission for 23 months.

Keywords:

metastases
children
Ewing sarcoma

Authors:

Sanakoeva A.V.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Samarin A.E.

Kommunarka Moscow Multidi-Field Clinical Center

Konopleva E.I.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Tarakanova A.V.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Sidorov I.V.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Druy A.E.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology;
Institute of Medical Cell Technologies

Karachunsky A.I.

Dmitry Rogachev National Medical Research Center for Pediatric Hematology, Oncology and Immunology

Received:

15.08.2024

Accepted:

30.01.2025

Close metadata

References:

  1. Hamilton SN, Carlson R, Hasan H, Rassekh SR, Goddard K. Long-term outcomes and complications in pediatric Ewing sarcoma. American journal of clinical oncology. 2017;40(4):423-428.  https://doi.org/10.1097/COC.0000000000000176
  2. Irfan M, Abdelsamad O, Grezenko H, Patel A, Akram MR. Brain metastasis with a solitary lesion secondary to knee joint Ewing sarcoma: A Case Report. Cureus. 2023;15(5):e39612. https://doi.org/10.7759/cureus.39612
  3. Riggi N, Suvà ML, Stamenkovic I. N Ewing’s sarcoma. New England Journal of Medicine. 2021;384(2):154-164.  https://doi.org/10.1056/NEJMra2028910
  4. Guoqi L, Piao Z, Wenkan Z, Zhong L, Jiaming H, Jiahong M,Tuoyo D, Weiqi Y. Identification of key genes and pathways in Ewing’s sarcoma patients associated with metastasis and poor prognosis. OncoTargets and Therapy. 2019;27(12):4153-4165  https://doi.org/10.2147/OTT.S195675
  5. Zhang L, Xiong L, Wu LM, Shen WH, Zhou P, Lian CL, Zhang WT, Wu SG. The patterns of distant metastasis and prognostic factors in patients with primary metastatic Ewing sarcoma of the bone. Journal of Bone Oncology. 2021;30:100385.
  6. Curless RG, Toledano SR, Ragheb J, Cleveland WW, Falcone S. Hematogenous brain metastasis in children. Pediatric Neurology. 2002;26(3):219-221.  https://doi.org/10.1016/s0887-8994(01)00363-0.
  7. Hesla AC, Papakonstantinou A, Tsagkozis P. Current Status of Management and Outcome for Patients with Ewing Sarcoma. Cancers. 2021;13(6):1202. https://doi.org/10.3390/cancers13061202
  8. Bekiesinska-Figatowska M, Duczkowska A, Duczkowski M, Bragoszewska H, Romaniuk-Doroszewska A, Iwanowska B, Szkudlinska-Pawlak S, Madzik J, Bilska K, Raciborska A. CNS metastases from bone and soft tissue sarcomas in children, adolescents, and young adults: Are they really so rare?. BioMed Research International. 2017;2017:1456473. https://doi.org/10.1155/2017/1456473
  9. Fox BD, Patel A, Suki D, Rao G. Surgical management of metastatic sarcoma to the brain: Clinical article. Journal of Neurosurgery. 2009;110(1):181-186.  https://doi.org/10.3171/2008.4.17505
  10. Chan CM, Lindsay AD, Spiguel AR, Scarborough MT, Gibbs CP. Brain metastases from Truncal and extremity bone and soft tissue sarcoma: Single institution study of oncologic outcomes. Rare Tumors. 2020;12:2036361320960060. https://doi.org/10.1177/2036361320960060
  11. Shweikeh F, Bukavina L, Saeed K, Sarkis R, Suneja A, Sweiss F, Drazin D. Brain metastasis in bone and soft tissue cancers: a review of incidence, interventions, and outcomes. Sarcoma. 2014;2014:475175. https://doi.org/10.1155/2014/475175
  12. Ferrari S, Luksch R, Hall KS, Fagioli F, Prete A, Tamburini A, Tienghi A, DiGirolamo S, Paioli A, Abate ME, Podda M, Cammelli S, Eriksson M, Brach del Prever A. Post‐relapse survival in patients with Ewing sarcoma. Pediatric blood & cancer. 2015;62(6):994-999.  https://doi.org/10.1002/pbc.25388
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