Published September 16, 2019 | Version v1
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Pseudohemangioma of the head - diagnostic difficulties in a pediatric patient with Ewing's sarcoma of the scalp: case report

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Borowik Joanna, Kuśmierczuk Kinga, Brodowski Wojciech, Kozak Katarzyna, Jawoszek Patryk, Zaucha-Prażmo Agnieszka. Pseudohemangioma of the head - diagnostic difficulties in a pediatric patient with Ewing’s sarcoma of the scalp: case report. Journal of Education, Health and Sport. 2019;9(9):513-525. eISSN 2391-8306. DOI http://dx.doi.org/10.5281/zenodo.3417064

http://ojs.ukw.edu.pl/index.php/johs/article/view/7455

 

 

 

 

 

The journal has had 5 points in Ministry of Science and Higher Education parametric evaluation. § 8. 2) and § 12. 1. 2) 22.02.2019.

 

© The Authors 2019;

This article is published with open access at Licensee Open Journal Systems of Kazimierz Wielki University in Bydgoszcz, Poland

Open Access. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author (s) and source are credited. This is an open access article licensed under the terms of the Creative Commons Attribution Non commercial license Share alike.

(http://creativecommons.org/licenses/by-nc-sa/4.0/) which permits unrestricted, non commercial use, distribution and reproduction in any medium, provided the work is properly cited.

The authors declare that there is no conflict of interests regarding the publication of this paper.

Received: 25.08.2019. Revised: 30.08.2019. Accepted: 14.09.2019.

 

 

 

 

 

 

 

 

 

 

Pseudohemangioma of the head - diagnostic difficulties in a pediatric patient with Ewing’s sarcoma of the scalp: case report


 

Borowik Joanna Urszula, joannaa.borowik@gmail.com, Students’ Research Group at the Department of Hematology, Oncology and Pediatric Transplantology, Medical University of Lublin, Profesor Antoni Gębala Street 6, 20-093 Lublin, Poland

Kuśmierczuk Kinga, kinga.kusmierczuk@gmail.com, Students’ Research Group at the Department of Hematology, Oncology and Pediatric Transplantology, Medical University of Lublin, Profesor Antoni Gębala Street 6, 20-093 Lublin, Poland

Brodowski Wojciech, brodowski.wojciech@gmail.com, Students’ Research Group at the Department of Hematology, Oncology and Pediatric Transplantology, Medical University of Lublin, Profesor Antoni Gębala Street 6, 20-093 Lublin, Poland

Kozak Katarzyna Anna, katarzyna.kozak95@gmail.com, Students’ Research Group at the Department of Hematology, Oncology and Pediatric Transplantology, Medical University of Lublin, Profesor Antoni Gębala Street 6, 20-093 Lublin, Poland

Jawoszek Patryk, patryk.jawoszek@gmail.com, Students’ Research Group at the Department of Hematology, Oncology and Pediatric Transplantology, Medical University of Lublin, Profesor Antoni Gębala Street 6, 20-093 Lublin, Poland

Zaucha-Prażmo Agnieszka, agnieszkazauchaprazmo@umlub.pl, Department of Hematology, Oncology and Pediatric Transplantology, Medical University of Lublin, Profesor Antoni Gębala Street 6, 20-093 Lublin, Poland


 

Abstract

Introduction: Ewing’s sarcoma (ES) is the second most common malignant bone tumor of childhood and adolescence. Typically, ES affects the long bones, pelvis and the trunk. Primary location in the scalp is rare.

Aim of study: The aim of our study is to focus on the case of a pediatric patient with Ewing's sarcoma located in the scalp, which adopted a cavernous angioma mask, and to assess the available knowledge on the diagnosis and treatment of the extracostal ES located in the scalp.

Material and methods: The research method was a case study. The research material was the patient's medical record, and the technique used was an analysis. An unsystematic review of Polish and English-language scientific literature was conducted. Electronic databases: PubMed, SCOPUS and Google Scholar were searched using the keywords: sarcoma, Ewing, hemangioma, pseudohemangioma, the head, the scalp.

Results: When the girl was 6 months old, a tubercle appeared on her head. It was asymptomatic, but gradually increased. Imaging studies suggested the diagnosis of cavernous hemangioma. The tumor did not respond to treatment and still was growing. A decision was made to include resection. The upward tumor underwent histopathology with immunohistochemical assessment and genetic testing. The result pointed to extraskeletal Ewing’s sarcoma.

Conclusions: Despite the few cases described in the literature, remember about atypical locations of primary Ewing sarcoma such as scalp. Making the right diagnosis was a challenge for the multi-specialist team of doctors. Histopathological examination supplemented by immunohistochemical assessment and genetic testing gave a definitive diagnosis and enabled proper treatment.

Key words: sarcoma; Ewing; hemangioma; pseudohemangioma; the head; the scalp

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