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Highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis

PURPOSE: To evaluate the characteristics of highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis. MATERIALS AND METHODS: The clinical and radiological characteristics of 18 cases of highly malignant soft tissue sarcomas of the extremity with a delayed diagnosis were determi...

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Autores principales: Park, Jong Hoon, Kang, Chang Ho, Kim, Chul Hwan, Chae, In Jung, Park, Ji Hun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955565/
https://www.ncbi.nlm.nih.gov/pubmed/20863406
http://dx.doi.org/10.1186/1477-7819-8-84
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author Park, Jong Hoon
Kang, Chang Ho
Kim, Chul Hwan
Chae, In Jung
Park, Ji Hun
author_facet Park, Jong Hoon
Kang, Chang Ho
Kim, Chul Hwan
Chae, In Jung
Park, Ji Hun
author_sort Park, Jong Hoon
collection PubMed
description PURPOSE: To evaluate the characteristics of highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis. MATERIALS AND METHODS: The clinical and radiological characteristics of 18 cases of highly malignant soft tissue sarcomas of the extremity with a delayed diagnosis were determined. RESULTS: Ten men and eight women of mean age 44.8 years (range, 15-79 years) were included in this study. Seven cases of synovial sarcoma, three cases each of alveolar soft part sarcoma and malignant fibrous histiocytoma, two cases each of highly malignant leiomyosarcoma and myxofibrosarcoma, and one case of clear cell sarcoma were enrolled. Times from tumor detection to diagnosis ranged from 1 to 3 years in most cases; three of the seven synovial sarcoma cases took more than 10 years to diagnose. Of the seven cases of synovial sarcoma, five cases of small, superficial located masses were simply excised without a pre-surgical biopsy. Three cases of alveolar soft part sarcoma showed characteristic T1- and T2-weighted high signal intensities with signal voids in MR images. In addition, one synovial sarcoma patient and one alveolar soft part sarcoma patient showed evidence of calcification on plain radiographs. However, no general characteristic clinical findings were found to be common to the 18 cases. CONCLUSIONS: Contrary to general expectations, some soft tissue tumors that grow slowly are painless, and those that occur in superficial limbs may be highly malignant. Thus, even when a slow growing, painless superficial mass is encountered in a limb, physicians should keep the possibility of highly malignant soft tissue sarcoma in mind.
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spelling pubmed-29555652010-10-16 Highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis Park, Jong Hoon Kang, Chang Ho Kim, Chul Hwan Chae, In Jung Park, Ji Hun World J Surg Oncol Research PURPOSE: To evaluate the characteristics of highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis. MATERIALS AND METHODS: The clinical and radiological characteristics of 18 cases of highly malignant soft tissue sarcomas of the extremity with a delayed diagnosis were determined. RESULTS: Ten men and eight women of mean age 44.8 years (range, 15-79 years) were included in this study. Seven cases of synovial sarcoma, three cases each of alveolar soft part sarcoma and malignant fibrous histiocytoma, two cases each of highly malignant leiomyosarcoma and myxofibrosarcoma, and one case of clear cell sarcoma were enrolled. Times from tumor detection to diagnosis ranged from 1 to 3 years in most cases; three of the seven synovial sarcoma cases took more than 10 years to diagnose. Of the seven cases of synovial sarcoma, five cases of small, superficial located masses were simply excised without a pre-surgical biopsy. Three cases of alveolar soft part sarcoma showed characteristic T1- and T2-weighted high signal intensities with signal voids in MR images. In addition, one synovial sarcoma patient and one alveolar soft part sarcoma patient showed evidence of calcification on plain radiographs. However, no general characteristic clinical findings were found to be common to the 18 cases. CONCLUSIONS: Contrary to general expectations, some soft tissue tumors that grow slowly are painless, and those that occur in superficial limbs may be highly malignant. Thus, even when a slow growing, painless superficial mass is encountered in a limb, physicians should keep the possibility of highly malignant soft tissue sarcoma in mind. BioMed Central 2010-09-23 /pmc/articles/PMC2955565/ /pubmed/20863406 http://dx.doi.org/10.1186/1477-7819-8-84 Text en Copyright ©2010 Park et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Park, Jong Hoon
Kang, Chang Ho
Kim, Chul Hwan
Chae, In Jung
Park, Ji Hun
Highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis
title Highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis
title_full Highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis
title_fullStr Highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis
title_full_unstemmed Highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis
title_short Highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis
title_sort highly malignant soft tissue sarcoma of the extremity with a delayed diagnosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955565/
https://www.ncbi.nlm.nih.gov/pubmed/20863406
http://dx.doi.org/10.1186/1477-7819-8-84
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