Soft Tissue Sarcoma Flashcards
What are key features of soft tissue tumours?
Many have uncertain lineage
Arise from genetic changes rather than differentiated cells i.e. leads to tumours arise in area of cells completely different to tumour cell type
Associated with molecular abnormalities
What molecular abnormalities can give rise to soft tissue tumours?
Translocations
-new oncogenic fusion genes formed
Somatic mutations
Copy number abnormalities i.e. gene amplification or deletion
Complex unbalanced karyotypes
What broad categories of soft tisse tumour are there?
Apipocytic = fat-forming
- lipoma
- liposarcoma
Smooth muscle tumours
- leiomyoma
- leiomysarcoma
Nerve sheath tumours
- Schwannoma
- Malignant peripheral nerve sheath tumour
Vascular
- angiosarcoma
- kaposi sarcoma
Small round cell tumours
- Ewing sarcoma
- rhabdomyosarcoma
What is a lipoma?
What are key characteristics of this tumour?
Most common form of soft tissue tumour which can occur at any site
Resembles normal fat
Grows slowly
Benign
What is a liposarcoma?
Where does it most commonly occur?
How do they tend to affect?
What are the different types of liposarcoma?
Malignany fat-forming tumour and is most common soft tissue sarcoma
Peak age= 60-70 (WDL) and 20-60 for myxoid
Lower extremitites and retroperitoneum (patients can just think they’re putting on weight)
Well-differentiated liposarcoma (WDL)
- tumour cells resemble fat cells
- amplification leads to increased proliferation
De-differentiated liposarcoma (DDL)
-pleomorphic
Myxoid
-tumour resembles embyronic fat i.e. lipoblasts
What is a leiomyoma?
Where does it commonly occur and how would it present?
What is it treated?
Benign smooth muscle tumour
Uterus as fibroids
Extra-uterine soft tissue
Large lesions cause pain and bleeding
Excision is curative
What is a leiomyosarcoma?
Where does it commonly occur?
What factors can pre-dispose?
Malignant smooth muscle tumour
Uterus
Extra-uterine= limbs/retroperitoneum/large vessels
I.e. can grow in wall of veins and lead to venous occlusion
Oestrogen
Irradiation
Immune suppression i.e. EBV
What is a schwannoma?
Where does it occur?
When might a patient experience pain with this tumours?
What is the treatment?
Benign tumour of Schwann cells of the nerve sheath
Effects peripheral nerves
Pain when inpinges the nerve
Surgical excision of solitary lesions
What are the features of malignant peripheral nerve sheath tumours?
50% of them occur in neurofibromatosis type 1
Very rarely associated with schwannoma
Can present with mass with pain or parathesia due to nerve association
Can metastasise
What is an angiosarcoma?
When does it typically occur?
Aggressive vascular tumour which can present as haemorrhagic tumours infiltrating into SC
Develops on skin of elderly person due to increased sun exposure
What is a specific subtype of angiosarcoma?
Who develops this tumour?
Kaposi sarcoma
-locally destructive tumour of blood vessels
All cases associated with HHV-8
Commonly occurs in immunosuppresed patients
What are the aims of soft tissue tumour diagnosis?
Identify differentiation i.e. lineage
Predict the behaviour and malginant potential of tumour
Guide treatment
Assess progression
How do soft tissue tumours classically present?
Mass- can be painful or painless
Can cause parathesia or obstruction
Might have FH
Might have PMH of trauma/previous disease or therapy
Which soft tissue tumours are associated with childhood?
Neuroblastoma
Embyronal rhabdomyosarcoma
ALL
Which soft tissue tumours are associated with adulthood?
Small cell carcinoma
Small cell melanoma
Alveolar rhabdomyosarcoma
Ewing Sarcoma
Roud cell liposarcoma
Poorly differentiated synovial sarcoma
Endometrial stromal sarcoma