Types of soft tissue sarcoma
This page tells you about the different types of soft tissue sarcoma. There is information about
Types of soft tissue sarcoma
Soft tissue sarcomas can develop in any of the soft connective tissues of the body. So there are many different types including
- Fibrosarcomas that grow from fibrous body tissues
- Leiomyosarcomas and rhabdomyosarcomas that start in muscle cells
- Liposarcomas of fatty tissue
- Synovial sarcomas, which start near the joints of arms and legs
- Angiosarcomas that start in the walls of blood or lymphatic vessels
- MPNST – malignant peripheral nerve sheath tumours (PNSTs) that develop from the soft tissues that surround nerves
- GIST – gastrointestinal stromal sarcoma that develops in the digestive system
- Kaposi’s sarcoma of the skin
- Ewing's sarcomas and PNETs
You can view and print the quick guides for all the pages in the About soft tissue sarcoma section.
Fibrosarcomas grow from cells in fibrous tissue. The cells are called histiocytes or fibrocytes. There are different types of fibrous sarcoma. One is called malignant fibrous histiocytoma. Fibrous sarcomas can grow in any part of the body. But they are most commonly found in the arms or legs.
These sarcomas start in muscle cells. Leiomyosarcomas develop from smooth muscle cells. This is the type of muscle that you do not control voluntarily. So it is called involuntary muscle. It forms the walls of the womb, stomach, intestine and blood vessels.
Rhabdomyosarcomas develop from skeletal (striated) muscle cells. This is the type of muscle that you can control. Rhabdomyosarcomas are found most often in the arms and legs.
There are two main types of rhabdomyosarcoma – embryonal and alveolar. Embryonal rhabdomyosarcomas tend to occur more commonly in children and young people. Alveolar rhabdomyosarcomas tend to occur more often in younger adults. There is a third type called pleomorphic rhabdomyosarcoma. This is rare and tends to occur in adults.
These are sarcomas that develop from fatty tissue and can grow anywhere in the body. They usually show up as soft lumps.
These sarcomas are most commonly found around the knee, and they start in cells close to joints and tendons. They can be found anywhere in the body. These sarcomas usually show up as hard lumps but can be present for some time before they start to grow bigger. They are more common in young adults.
These are cancers of the cells that cover nerves. There are different types of MPNSTs including neurofibrosarcomas and malignant schwannomas. Schwannomas develop from the cells that form the fatty sheath which covers nerves. These cells are called schwann cells.
Gastrointestinal stromal tumours can be cancerous or non cancerous (benign). You may hear cancerous GIST called GI stromal sarcoma. Generally speaking, the larger the GIST, the more likely it is to be cancerous. These tumours develop from the cells of the connective tissues that support the organs of the digestive system – the gastrointestinal tract. Most are found in the stomach. GIST is treated differently from other types of soft tissue sarcoma.
Kaposi’s sarcoma develops from cells called endothelial cells. Most cases occur in the skin but it can also develop in internal organs of the body. Coloured nodules develop on the skin, in the mouth and lymph nodes, and in organs such as the lung, liver and spleen. It is very rare, with only 155 cases diagnosed in the UK in 2007.
Some types of Kaposi's sarcoma are known to be associated with HIV (human immunodeficiency virus) infection and AIDS (acquired immunodeficiency syndrome). It can be caused by a sexually transmitted virus called human herpes virus 8 (HHV8) or Kaposi's sarcoma herpes virus (KSHV). Other types are associated with Jewish, Italian and West African ancestry. Kaposi's sarcoma is treated differently to many soft tissue sarcomas and so is not covered in this section.
Ewings sarcomas occur more often in bone. But about a third of cases are found growing in soft tissues. PNET stands for primitive neuroectodermal tumour. It is a type of Ewings that can start in soft tissues. Both of these soft tissue tumours behave a bit differently to other types of soft tissue sarcoma.
Ewings sarcomas and PNETs are usually treated in the same way as bone tumours (osteosarcomas). You usually have chemotherapy to shrink the tumour, followed by surgery to remove it and sometimes radiotherapy after surgery. So you may find the bone tumour section more useful if you are looking for information about treatment for soft tissue Ewings or PNET.
Fibromatosis is not actually a sarcoma, but we have included it here because we are sometimes asked about it. Fibromatosis is not cancer. It does not spread around the body but these tumours can spread into nearby tissues. It is also called aggressive fibromatosis or a desmoid tumour. Fibromatosis is said to be halfway between a fibrosarcoma and a benign fibroma.
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