Unusual localization and aggressive progression of large infantile fibrosarcoma

Infantile fibrosarcoma is a very rare soft tissue tumor in infants and children most commonly located in extremities. It constitutes less then 1 percent of all childhood cancers. Prognosis and clinical course of it is relatively good compared to adult forms. Local recurrence is common but metastasis...

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Main Authors: İsmail Burak Atalay, Guray Togral
Format: Article
Language:English
Published: AVES Yayincilik 2019-11-01
Series:Acta Orthopaedica et Traumatologica Turcica
Online Access:http://www.sciencedirect.com/science/article/pii/S1017995X19303839
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spelling doaj-c32c3fe8525a4dcd80f3a0591d619c392020-11-25T03:33:07ZengAVES YayincilikActa Orthopaedica et Traumatologica Turcica1017-995X2019-11-01536507511Unusual localization and aggressive progression of large infantile fibrosarcomaİsmail Burak Atalay0Guray Togral1Corresponding author. Vatan caddesi, 06200, DemetevlerAnkara, Turkey. Tel.: +90 312 3360909/90 5056233356; fax: +90 312 3340352.; Department of Orthopaedics and Traumatology, DR A.Y Ankara Oncology Training and Research Hospital, Ankara, TurkeyDepartment of Orthopaedics and Traumatology, DR A.Y Ankara Oncology Training and Research Hospital, Ankara, TurkeyInfantile fibrosarcoma is a very rare soft tissue tumor in infants and children most commonly located in extremities. It constitutes less then 1 percent of all childhood cancers. Prognosis and clinical course of it is relatively good compared to adult forms. Local recurrence is common but metastasis is infrequent.In this case report we present infantile fibrosarcoma with relapse and lung metastasis despite neoadjuvant chemotherapy, pelvic reconstruction surgery with wide surgical excision and adjuvant chemotherapy protocol. The patient was a 2-year-old girl at the time of diagnosis, and there was a huge mass in pelvic region. After neoadjuvant chemotherapy, type 1 pelvic resection and pelvic reconstruction with bone cement performed. The patient presented with relapse and lung metastasis 6 months after the surgery.This is the first report of pelvic infantile fibrosarcoma with pelvic resection surgery. This case suggests that these tumors may exhibit unpredictable clinical behavior. Keywords: Infantile fibrosarcoma, Pelvic region, Distant metastasis, Surgical treatment, Chemotherapyhttp://www.sciencedirect.com/science/article/pii/S1017995X19303839
collection DOAJ
language English
format Article
sources DOAJ
author İsmail Burak Atalay
Guray Togral
spellingShingle İsmail Burak Atalay
Guray Togral
Unusual localization and aggressive progression of large infantile fibrosarcoma
Acta Orthopaedica et Traumatologica Turcica
author_facet İsmail Burak Atalay
Guray Togral
author_sort İsmail Burak Atalay
title Unusual localization and aggressive progression of large infantile fibrosarcoma
title_short Unusual localization and aggressive progression of large infantile fibrosarcoma
title_full Unusual localization and aggressive progression of large infantile fibrosarcoma
title_fullStr Unusual localization and aggressive progression of large infantile fibrosarcoma
title_full_unstemmed Unusual localization and aggressive progression of large infantile fibrosarcoma
title_sort unusual localization and aggressive progression of large infantile fibrosarcoma
publisher AVES Yayincilik
series Acta Orthopaedica et Traumatologica Turcica
issn 1017-995X
publishDate 2019-11-01
description Infantile fibrosarcoma is a very rare soft tissue tumor in infants and children most commonly located in extremities. It constitutes less then 1 percent of all childhood cancers. Prognosis and clinical course of it is relatively good compared to adult forms. Local recurrence is common but metastasis is infrequent.In this case report we present infantile fibrosarcoma with relapse and lung metastasis despite neoadjuvant chemotherapy, pelvic reconstruction surgery with wide surgical excision and adjuvant chemotherapy protocol. The patient was a 2-year-old girl at the time of diagnosis, and there was a huge mass in pelvic region. After neoadjuvant chemotherapy, type 1 pelvic resection and pelvic reconstruction with bone cement performed. The patient presented with relapse and lung metastasis 6 months after the surgery.This is the first report of pelvic infantile fibrosarcoma with pelvic resection surgery. This case suggests that these tumors may exhibit unpredictable clinical behavior. Keywords: Infantile fibrosarcoma, Pelvic region, Distant metastasis, Surgical treatment, Chemotherapy
url http://www.sciencedirect.com/science/article/pii/S1017995X19303839
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