Sarcoma
Sarcoma
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Sarcoma
, Soft Tissue Sarcoma
See Also
Soft Tissue Mass
Definitions
Sarcoma
Cancer arrising in mesenchymal (connective) tissue
Tumors may originate from bones, fat,
Muscle
, vessels or
Lymphatics
Derived from greek word "sar" meaning fleshy
Epidemiology
Age
More common in adults over age 35 years (but represent <1% of adult cancers)
Sarcomas represent 10-15% of childhood malignancy (esp. in extremities)
Soft Tissue Sarcomas are the sixth most common
Childhood Cancer
(esp. rhabomyosarcoma)
Types
Soft-tissue Sarcomas
Kaposi's Sarcoma
Hepatic angiosarcoma
Dermatofribosarcoma Protuberans
Synoviosarcoma
Rhabdomyosarcoma
Most common Soft Tissue Sarcoma in children (esp. age <8 years old)
Account for 60% of pediatric tumors of the head and neck
Leiomyosarcoma
Involves
Uterus
in adults
Involves
Retroperitoneum
in children
Liposarcoma
Rare adipose tumor (usually invades locally only)
Involves deep thigh or
Retroperitoneum
Fibrosarcoma
Most common Soft Tissue Sarcoma in age <1 year
Involves deep thigh or
Retroperitoneum
Vascular Sarcoma
Angiosarcoma (Stewart-Treves Syndrome)
Malignancy of blood vessels and lymph vessels
Presents with red to violaceous skin
Papule
s
May invade deeper tissue with tumor growth, leading to ulceration, edema, bleeding
Hemangioendothelioma
Hemangiopericytoma
Bone Tumor
s
Ewing's Sarcoma
Osteogenic Sarcoma
Precautions
See
Soft Tissue Mass
for red flag findings
Delayed presentation is common (often >1 month from finding a
Soft Tissue Mass
)
Most Soft Tissue Sarcomas gradually enlarge without pain or constitutional symptoms
Evaluation
See
Soft Tissue Mass
(includes red flag findings and imaging)
Prognosis
Five year survival: 60%
Ranges between Stage 1 (five year survival 80%) and Stage 4 (five year survival 20%)
References
Hanback and Kosoko (2023) Crit Dec Emerg Med 37(4): 14-5
Achar (2022) Am Fam Physician 105(6): 602-12 [PubMed]
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