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Extraskeletal Ewing's Sarcoma Masquerading as Infantile Benign Neck Mass

Despite being the second most common malignant bone tumor, Ewing's sarcoma remains uncommon in younger children and seldom seen in neonates and infants. Extraskeletal locations are even rarer, hardly ever suspected, and often misdiagnosed, causing delays in management. The histologic similariti...

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Autores principales: Gazula, Suhasini, Rani, V. Leela, Jonathan, G. T., Kumar, N. Narender
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6568164/
https://www.ncbi.nlm.nih.gov/pubmed/31258273
http://dx.doi.org/10.4103/jiaps.JIAPS_98_18
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author Gazula, Suhasini
Rani, V. Leela
Jonathan, G. T.
Kumar, N. Narender
author_facet Gazula, Suhasini
Rani, V. Leela
Jonathan, G. T.
Kumar, N. Narender
author_sort Gazula, Suhasini
collection PubMed
description Despite being the second most common malignant bone tumor, Ewing's sarcoma remains uncommon in younger children and seldom seen in neonates and infants. Extraskeletal locations are even rarer, hardly ever suspected, and often misdiagnosed, causing delays in management. The histologic similarities of Ewing's sarcoma to more common pediatric small-blue-round-cell tumors such as lymphoma and neuroblastoma necessitate immunohistochemistry and molecular genetics for clinching the diagnosis. We report a soft-tissue Ewing's sarcoma in a 4-month-old female infant masquerading as a benign neck mass clinically, radiologically, cytologically, and intraoperatively. We also reviewed literature for any existing guidelines on when to biopsy neck masses in the pediatric population.
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spelling pubmed-65681642019-07-01 Extraskeletal Ewing's Sarcoma Masquerading as Infantile Benign Neck Mass Gazula, Suhasini Rani, V. Leela Jonathan, G. T. Kumar, N. Narender J Indian Assoc Pediatr Surg Case Report Despite being the second most common malignant bone tumor, Ewing's sarcoma remains uncommon in younger children and seldom seen in neonates and infants. Extraskeletal locations are even rarer, hardly ever suspected, and often misdiagnosed, causing delays in management. The histologic similarities of Ewing's sarcoma to more common pediatric small-blue-round-cell tumors such as lymphoma and neuroblastoma necessitate immunohistochemistry and molecular genetics for clinching the diagnosis. We report a soft-tissue Ewing's sarcoma in a 4-month-old female infant masquerading as a benign neck mass clinically, radiologically, cytologically, and intraoperatively. We also reviewed literature for any existing guidelines on when to biopsy neck masses in the pediatric population. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6568164/ /pubmed/31258273 http://dx.doi.org/10.4103/jiaps.JIAPS_98_18 Text en Copyright: © 2019 Journal of Indian Association of Pediatric Surgeons http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Gazula, Suhasini
Rani, V. Leela
Jonathan, G. T.
Kumar, N. Narender
Extraskeletal Ewing's Sarcoma Masquerading as Infantile Benign Neck Mass
title Extraskeletal Ewing's Sarcoma Masquerading as Infantile Benign Neck Mass
title_full Extraskeletal Ewing's Sarcoma Masquerading as Infantile Benign Neck Mass
title_fullStr Extraskeletal Ewing's Sarcoma Masquerading as Infantile Benign Neck Mass
title_full_unstemmed Extraskeletal Ewing's Sarcoma Masquerading as Infantile Benign Neck Mass
title_short Extraskeletal Ewing's Sarcoma Masquerading as Infantile Benign Neck Mass
title_sort extraskeletal ewing's sarcoma masquerading as infantile benign neck mass
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6568164/
https://www.ncbi.nlm.nih.gov/pubmed/31258273
http://dx.doi.org/10.4103/jiaps.JIAPS_98_18
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