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Infantile Fibrosarcoma in a Child: a Case Report

BACKGROUND: Infantile Fibrosarcoma is a rare soft tissue tumor in infants and children mostly located in extremities. An infantile and adult form has similar histopathological patterns but survival prognosis is much better in infantile form. Recurrence of infantile fibrosarcoma is common but the rat...

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Autores principales: Hashemi, A, Tefagh, S, Seifadini, A, Moghimi, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shahid Sadoughi University of Medical Sciences 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921878/
https://www.ncbi.nlm.nih.gov/pubmed/24575285
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author Hashemi, A
Tefagh, S
Seifadini, A
Moghimi, M
author_facet Hashemi, A
Tefagh, S
Seifadini, A
Moghimi, M
author_sort Hashemi, A
collection PubMed
description BACKGROUND: Infantile Fibrosarcoma is a rare soft tissue tumor in infants and children mostly located in extremities. An infantile and adult form has similar histopathological patterns but survival prognosis is much better in infantile form. Recurrence of infantile fibrosarcoma is common but the rates of metastasis are less than 10 percent in children younger than five Years and 50 percent in children more than 10 years old. CASE PRESENTATION: In this case report, we presented a nine years girl with a relapsing mass in her left hand. The pathologic findings showed sheets of spindle-shaped cells with suggested diagnose of infantile fibrosarcoma. She was successfully treated with combination of surgery and chemotherapy with a good outcome. CONCLUSION: Infantile fibrosarcoma is a differential diagnose of soft tissue mass in infants and children. It has a good prognosis and distant metastasis is uncommon. Choice of treatment is surgery but chemotherapy and radiotherapy were useful in decrease metastasis.
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spelling pubmed-39218782014-02-26 Infantile Fibrosarcoma in a Child: a Case Report Hashemi, A Tefagh, S Seifadini, A Moghimi, M Iran J Ped Hematol Oncol Case Report BACKGROUND: Infantile Fibrosarcoma is a rare soft tissue tumor in infants and children mostly located in extremities. An infantile and adult form has similar histopathological patterns but survival prognosis is much better in infantile form. Recurrence of infantile fibrosarcoma is common but the rates of metastasis are less than 10 percent in children younger than five Years and 50 percent in children more than 10 years old. CASE PRESENTATION: In this case report, we presented a nine years girl with a relapsing mass in her left hand. The pathologic findings showed sheets of spindle-shaped cells with suggested diagnose of infantile fibrosarcoma. She was successfully treated with combination of surgery and chemotherapy with a good outcome. CONCLUSION: Infantile fibrosarcoma is a differential diagnose of soft tissue mass in infants and children. It has a good prognosis and distant metastasis is uncommon. Choice of treatment is surgery but chemotherapy and radiotherapy were useful in decrease metastasis. Shahid Sadoughi University of Medical Sciences 2013 2013-07-22 /pmc/articles/PMC3921878/ /pubmed/24575285 Text en © 2013: Iranian Journal of Pediatric Hematology Oncology This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Hashemi, A
Tefagh, S
Seifadini, A
Moghimi, M
Infantile Fibrosarcoma in a Child: a Case Report
title Infantile Fibrosarcoma in a Child: a Case Report
title_full Infantile Fibrosarcoma in a Child: a Case Report
title_fullStr Infantile Fibrosarcoma in a Child: a Case Report
title_full_unstemmed Infantile Fibrosarcoma in a Child: a Case Report
title_short Infantile Fibrosarcoma in a Child: a Case Report
title_sort infantile fibrosarcoma in a child: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921878/
https://www.ncbi.nlm.nih.gov/pubmed/24575285
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AT tefaghs infantilefibrosarcomainachildacasereport
AT seifadinia infantilefibrosarcomainachildacasereport
AT moghimim infantilefibrosarcomainachildacasereport