ArticleTurkish archives of otorhinolaryngology2020
Ewing Sarcoma of Larynx: A Rare Case in a 5-Year-Old Boy.
Article in Turkish archives of otorhinolaryngology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 10 citations in OpenAlex.
- Laryngeal Preservation in Extraosseous Ewing's Sarcoma of the Larynx: A Case Report and Review of the Literature.Cureus · 2026Article
- Cervical extraosseous Ewing's sarcoma: A case report.Radiology case reports · 2025Article
- Extraosseous Ewing's Sarcoma Masquerading as Adolescent Neck Mass-a Case Report and Review of Literature.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2024Article
- Primitive Neuroectodermal Tumour of the Larynx: A Rare Case Report.Indian journal of surgical oncology · 2024Article
- Primary Cervical Extraosseous Ewing's Sarcoma Originated from the Sternocleidomastoid Muscle: A Case Report and Review of the Literature.Case reports in otolaryngology · 2024Article
- Fluoro-18-fluorodeoxyglucose positron emission tomography/computed tomography detects Ewing's sarcoma of the larynx with multiple distant bone metastases: a case report and literature review.Frontiers in medicine · 2023Article
- Larynx cancer diagnosed as Ewing Sarcoma in a 41-year-old man: A case report.Annals of medicine and surgery (2012) · 2022Article
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Authors and funding
5 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
Ewing Sarcoma of the head and neck region is an extremely rare entity. Treatment usually involves surgery, chemotherapy and radiotherapy in varying sequences. We present the third case to date of Ewing sarcoma of the larynx in a paediatric population. A 5-year-old boy presented to emergency room with acute respiratory distress. Computerized tomography scan showed a mass in the supraglottis; he was intubated using videolaryngoscope and tracheostomy was avoided, mass was removed by cold dissection. Final histopathologic examination revealed Ewing sarcoma. Further workup showed no systemic metastasis. Patient was advised adjuvant therapy which the family refused. Currently he is doing fine on 2 years of follow-up.
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