Leptomeningeal canceromatosis in patient with parameningeal rhabdomyosarcoma

Author:

Kazakova L. L.1ORCID,Zhukov N. V.2ORCID

Affiliation:

1. Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation

2. Dmitriy Rogachev National Medical Research Center of Pediatric Hematology, Oncology, Immunology Ministry of Healthcare of Russian Federation; N.I. Pirogov Russian National Research Medical University

Abstract

The development of leptomeningeal carcinomatosis (LC) is quite a frequent event during a rhabdomyosarcoma with parameningeal localization, usually known as a parameningeal rhabdomyosarcoma (PM RMS). However, the diagnosis and treatment of this kind of progression are still difficult for pediatricians and pediatric oncologists due to the small absolute number of PM RMS patients, which makes it impossible to accumulate sufficient clinical experience, as well as due to the absence of a pathognomonic clinical picture and a standardized specific therapy. The article describes 3 clinical cases of LC during PM RMS and provides an overview of existing literature focusing on this problem. Parents patients agreed to use personal data in research and publications.

Publisher

Fund Doctors, Innovations, Science for Children

Subject

Oncology,Hematology,Immunology,Immunology and Allergy,Pediatrics, Perinatology, and Child Health

Reference22 articles.

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3. Siegel R.L., Miller K.D., Ahmedin J. Cancer statistics, 2019. CA Cancer J Clin 2019; 69: 7–34. DOI: 10.3322/caac.21551.

4. Yang B.A., Wexler L.H., Meyers P.A., Wolden S.L. Parameningeal Rhabdomyosarcoma: Outcomes and Opportunities. Int J Radiat Oncol Biol Phys 2013; 61–6. DOI: 10.1016/j.ijrobp.2012.08.019

5. Grewal J., Harpreet K., Grewal M.D. Leptomeningeal metastasis Copyright© 2001–2018 MedLink Corporation. All rights reserved.

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