ArticleBMJ case reports2020
Extra-skeletal Ewing's sarcoma of the frontal sinus: a rare disorder in pediatric age.
Article in BMJ case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
6 citing papers in PubMed, 10 citations in OpenAlex.
- Muscular Cystic Lesions: A Highly Misdiagnosed Extraosseous Ewing Sarcoma: Two Case Reports and Literature ReviewCurrent medical imaging · 2025Review
- Pediatric Extra-skeletal Sinonasal Ewing's Sarcoma: Report of Two Cases with Literature Review.Indian journal of surgical oncology · 2024Article
- Sinonasal Malignancies Involving the Frontal Sinus: A Mono-Institutional Experience of 84 Cases and Systematic Literature Review.Journal of clinical medicine · 2023Review
- Extraosseous Ewing Sarcoma in Children: A Systematic Review and Meta-Analysis of Clinicodemographic Characteristics.Children (Basel, Switzerland) · 2022Review
- Congenital Extraskeletal Ewing's Sarcoma over Forehead.Journal of Indian Association of Pediatric SurgeonsArticle
- Ewing's Sarcoma Presenting in the Paranasal Sinus - A Case Report.Annals of maxillofacial surgeryArticle
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Paediatric sinonasal tumours comprise numerous aetiologies. Ewing's sarcoma (ES) consists of a malignancy of neuroectodermal origin. This type of sarcoma affects mainly children and adolescents and can assume the skeletal or extra-skeletal form. Primary ES of head and neck is extremely rare, accounting for only 4%-9% of all cases. So far, as much as we know, only a few cases of sinonasal ES have been reported in literature. The authors present a case of a previous healthy 12-year-old girl who presented with a rapidly growing and expansive frontal mass and unilateral nasal obstruction. Immunohistochemical, molecular and cytogenetic analysis of the lesion showed diffuse expression of CD56 and CD99 on tumour cells and a translocation involving chromosome 22q12, confirming ES diagnosis.
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Registered trials
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