University Emergency Hospital Bucharest, Romania
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University Emergency Hospital Bucharest, Romania
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University Emergency Hospital Bucharest, Romania
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Elias University Emergency Hospital, Bucharest, Romania
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Elias University Emergency Hospital, Bucharest, Romania
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University Emergency Hospital Bucharest, Romania
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Introduction Soft tissue sarcomas (STS) represent a heterogeneous group of malignancies that are all distinguished by mesodermal differentiation, with unique clinical and pathologic characteristics. Only 1% of adult malignancies are STS, which
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Soft-tissue swellings, lumps and bumps are frequently seen in routine clinical practice. However, with an estimated annual incidence of five cases per 100 000 people in Europe, soft-tissue sarcomas (STS) are relatively rare and are outnumbered by
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Introduction Soft tissue sarcomas (STS) and bone sarcomas constitute rare mesenchymal neoplasms, with an incidence of 4.7 and 0.8 per 100 000 patients per year in Europe, respectively. 1 , 2 The majority of these tumours are located in
University of Basel, Basel, Switzerland
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The Bone and Soft Tissue Tumor Center of the University of Basel (KWUB), Basel, Switzerland
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Department of Radiology, University Hospital Basel, Basel, Switzerland
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Clarunis, University Digestive Health Care Center, St. Clara Hospital and University Hospital Basel, Switzerland
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The Bone and Soft Tissue Tumor Center of the University of Basel (KWUB), Basel, Switzerland
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Introduction Synovial sarcoma (SS) is a relatively rare malignancy, accounting for 5–10% of all soft tissue sarcomas (STS) ( 1 ). All SSs are considered to be high-grade STS, characterized by local invasiveness and a propensity to metastasize
These authors contributed equally to this manuscript
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These authors contributed equally to this manuscript
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These authors contributed equally to this manuscript
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also calcified lesions but without ‘zonal’ calcification. 3 Post-traumatic MO presents clinically with symptoms that simulate bone or soft tissue malignancies. The opposite is also true, because bone or soft tissue sarcomas, especially when there
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followed up in dermatology departments. Diagnosis of bone and soft-tissue foot tumours is often delayed and many malignant conditions are referred to specialised sarcoma teams after an initial inappropriate procedure. 4 - 6 The adverse effect of
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reconstruction of the soft tissues and a hemiarthroplasty should be best chosen to reduce instability. 10 Corresponding to this, Du et al investigated hip instability in 58 patients with total femoral replacement for sarcoma. 11 In 12 patients, a LARS
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Soft tissue sarcomas (STS) are rare, with a combined incidence of about 60/100,000 population a year. It is generally stated that there are 100 benign soft tissue tumours for every soft tissue sarcoma. As a result of this there is a low level of
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conservative approach is usually advocated. However, in cases of outsized tumours that may cause symptoms, excision or embolization is recommended. 75 Malignant soft tissue tumours of the elbow The incidence of soft tissue sarcomas (STS) in the
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cells (cytology and/or cultures). Usually the needle is guided by ultrasound and several passes may be used to increase yield. This is usually performed under local anaesthetic. This technique is particularly useful in high-grade soft-tissue sarcoma