Literature DB >> 25207328

Prevalence of malignant soft tissue tumors in extremities: an epidemiological study in syria.

Habib Reshadi1, Alireza Rouhani1, Saeid Mohajerzadeh1, Marvan Moosa1, Asghar Elmi1.   

Abstract

BACKGROUND: Although the majority of soft tissue masses are benign, it is important to consider malignancy in differential diagnoses. Because most soft tissue sarcomas present as a painless mass, clinicians must watch for signs suggestive of malignancy, including large size, rapid growth, and site deep into the deep fascia. The purpose of this study was to determine the relative prevalence according to sex and age, site of tumor, skeletal distribution, and treatment (surgery, chemotherapy and radiotherapy) before and after surgery, and ascertain the relative frequency of these tumors in specific anatomic sites and age groups based on pathological studies.
METHODS: A total of 308 patients, with a musculoskeletal tumor were evaluated retrospectively. All of the patients enrolled into this study were referred to the Beirouni Hospital of Damascus University with a proven diagnosis of malignant soft tissue tumors from the beginning of January 2008 until the end of 2010. The prevalence of the malignant soft tissue tumors in these patients was analyzed. For purposes of analysis, all lesions were placed in 1 of 9 categories: hand and wrist, forearm, humorous (arm), proximal limb girdle (axilla and shoulder), foot and ankle, thigh, hip and buttocks region, trunk, and other lesions. Age and sex also were recorded.
RESULTS: MALIGNANT TUMORS CONSISTED OF SEVEN DIAGNOSTIC CATEGORIES: malignant fibrous histiocytoma (23%), liposarcoma (22%), rhabdomyosarcoma (9%), leiomyosarcoma (8%), malignant schwannoma (5%), dermatofibrosarcoma protuberans (5%), synovial sarcoma (10%), fibrosarcoma (13%), extraskeletal chondrosarcoma (1%), and extraskeletal Ewing sarcoma (4%).
CONCLUSIONS: Despite the multitude of pathologic possibilities, most malignant soft-tissue tumors are classified into a small number of diagnoses. These may be further defined when the site of the lesion and the age of the patient are considered. Knowledge of tumor prevalence will assist radiologists in establishing a suitably ordered differential diagnosis when a soft-tissue tumor has a nonspecific radiologic appearance.

Entities:  

Keywords:  Oncology; Sarcoma; Syria

Year:  2014        PMID: 25207328      PMCID: PMC4151447     

Source DB:  PubMed          Journal:  Arch Bone Jt Surg        ISSN: 2345-461X


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  3 in total

1.  Soft Tissue Sarcoma of Extremities: Descriptive Epidemiological Analysis According to National Population-based Study.

Authors:  Adel Ebrahimpour; Mohammadreza Chehrassan; Mehrdad Sadighi; Amin Karimi; Mehdi Azizmohammad Looha; Meisam Jafari Kafiabadi
Journal:  Arch Bone Jt Surg       Date:  2022-01

2.  Atrophic dermatofibrosarcoma protuberans with the fusion gene COL1A1-PDGFB detected by RT-PCR using only a single primer pair.

Authors:  Wen-Jun Xu; Ju-Sheng Wang
Journal:  Int J Clin Exp Pathol       Date:  2015-06-01

3.  Reduction in Acquisition Time and Improvement in Image Quality in T2-Weighted MR Imaging of Musculoskeletal Tumors of the Extremities Using a Novel Deep Learning-Based Reconstruction Technique in a Turbo Spin Echo (TSE) Sequence.

Authors:  Daniel Wessling; Judith Herrmann; Saif Afat; Dominik Nickel; Ahmed E Othman; Haidara Almansour; Sebastian Gassenmaier
Journal:  Tomography       Date:  2022-07-06
  3 in total

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