Examples of 'tissue sarcomas' in a sentence
Meaning of "tissue sarcomas"
Tissue sarcomas: A type of cancer that begins in the soft tissues of the body, such as muscles or fat. It is a rare form of cancer that can be difficult to treat
How to use "tissue sarcomas" in a sentence
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tissue sarcomas
Soft tissue sarcomas are very rare.
This page explains soft tissue sarcomas in particular.
Soft tissue sarcomas are malignant tumours of mesenchymal origin.
It is one of the soft tissue sarcomas.
Bone and soft tissue sarcomas are the leading types of sarcoma.
Diagnostic methods and principles of treatment of patients with soft tissue sarcomas.
The cause of soft tissue sarcomas is mostly unknown.
Radiation exposure for other cancers can increase the risk of soft tissue sarcomas.
Risk of soft tissue sarcomas and residence near incinerator of industrial wastes.
Surgery is the main treatment of soft tissue sarcomas when they are located.
In soft tissue sarcomas and leukemias the dedifferentiation process of EMT does not occur.
Professor Bonvalot will be there to present her work on Soft Tissue Sarcomas.
Treatment for soft tissue sarcomas is determined mainly by the stage of the disease.
The main types of treatment for soft tissue sarcomas are,.
Patients with extremity soft tissue sarcomas are selected for treatment using the inventive method.
See also
In some aspects, the disclosure relates to treatment of soft tissue sarcomas.
His clinical practice is limited to soft tissue sarcomas with a special interest in retroperitoneal sarcomas.
However, a broad panel of antibodies is necessary to classify soft tissue sarcomas correctly.
The most common soft tissue sarcomas in adults are,.
Soft tissue sarcomas are hard to spot, because they can grow anywhere in your body.
Although they may be found in children, soft tissue sarcomas are more common in adults.
Moreover, soft tissue sarcomas are considered chemosensitive in both human and veterinary medicine.
There are mainly two major types of sarcomas, soft tissue sarcomas and osteosarcomas.
Soft tissue sarcomas are very serious, especially if diagnosed when the disease is more advanced.
Nearly one in five soft tissue sarcomas occur in the patient 's belly.
External radiation therapy is the most well-established risk factor for soft tissue sarcomas.
The 5-year survival rates for soft tissue sarcomas have not changed much for many years.
Currently, several factors have been identified that increase the risk of developing soft tissue sarcomas.
Metastasis, soft tissue sarcomas are characterized by,.
Genetic syndromes, Certain inherited conditions increase a person 's risk of developing soft tissue sarcomas.
Soft tissue sarcomas are rare tumors, representing approximately 1 % of malignant neoplasias in adults.
Sarcomas are divided into two main groups, bone tumours and soft tissue sarcomas STS.
Uh, management of soft tissue sarcomas in the upper limbs … amputation or limb-sparing surgery?
WJSO, Feasibility of chemosensitivity testing in soft tissue sarcomas.
There are other soft tissue sarcomas in adults, such as liposarcomas, histiocytomas, angiosarcomas, and leiomiosarcomas.
FDA approves Yondelis ( trabectedin ) for treatment of specific soft tissue sarcomas.
Soft tissue sarcomas are described as stages I-IV, based on the above findings.
Over 50 % of head and neck malignant tumors in children are soft tissue sarcomas and lymphomas.
Soft tissue sarcomas ( STS ) are rare tumors characterized by great anatomic, histological and prognostic heterogeneity.
Despite being a relatively rare cancer, it accounts for approximately 40 % of all recorded soft tissue sarcomas.
There are about 50 different types of soft tissue sarcomas ( not all are listed here ).
Doxorubicin has achieved response rates in the 12-23 % range for patients with soft tissue sarcomas.
It makes up about 20 % of all soft tissue sarcomas in adults.
Ray-Coquard et al . have demonstrated 95 % accuracy of CNB in the diagnosis of soft tissue sarcomas.
It is divided into two groups, bone tumours and soft tissue sarcomas ( STS ).
It accounts for over 50 % of all pediatric soft tissue sarcomas.
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