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Clinical presentation of childhood soft tissue sarcomas: a systematic review and meta-analysis
Lorna Ni Cheallaigh1, Jo-Fen Liu2, Lorna Fern3
1Institute of Child Health, University College London, London, UK.
Insights
Early detection of childhood soft tissue sarcoma (soft tissue sarcoma) is crucial for survival. Symptoms vary by tumor location and child's age, necessitating tailored diagnostic approaches.
Area of Science:
- Pediatric Oncology
- Symptomatology
- Diagnostic Interventions
Background:
- Time to diagnosis (TTD) in childhood soft tissue sarcoma (STS) significantly impacts patient survival.
- Identifying pre-diagnostic symptoms and signs is vital for developing earlier diagnosis interventions.
Approach:
- A comprehensive literature search was conducted across Medline, Embase, Cochrane, and Web-of-Science databases from January 2010 to February 2021.
- Studies involving children (<18 years) diagnosed with STS were included, with no language restrictions.
- Pooled proportions of symptoms and signs were calculated and analyzed based on tumor location and patient age.
Key Points:
- Lump/swelling (38%) was the most common symptom across all STS cases.
- Head and neck STS frequently presented with eye swelling (20%) and cranial nerve deficits (14%).
- Abdomen/pelvic STS commonly showed urinary symptoms (24%) and abdominal distension (22%).
- In younger children (<5 years), consumptive coagulopathy (16%) and cutaneous changes (5%) were more frequent.
- Older children (>11 years) more often presented with lumps/swelling, constitutional symptoms, pain, and headaches.
Conclusions:
- Pre-diagnostic symptoms of STS in children are diverse and influenced by both tumor location and patient age.
- These variations underscore the critical need for age- and location-specific early diagnosis strategies for childhood STS.
Background:
Time to diagnosis (TTD) of childhood soft tissue sarcoma (STS) is significantly associated with survival. This review aims to identify pre-diagnostic symptoms/signs to inform earlier diagnosis interventions.
Methods:
Medline, Embase, Cochrane and Web-of-Science were searched between January 2010 and February 2021 for studies including children (<18 years) diagnosed with STS, with no language restrictions. Pooled proportions of symptoms/signs were calculated and subanalysed by tumour location and age.
Results:
Fifty-nine eligible studies were identified, totalling 2462 cases. The most frequent symptoms were lump/swelling (38%, 95% CI 27% to 51%), pain (6%, 95% CI 3% to 10%), cutaneous changes (4%, 95% CI 0 to 9%), localised eye swelling (3%, 95% CI 0 to 7%), cranial nerve deficits (2%, 95% CI 0 to 5%) and constitutional symptoms (2%, 95% CI 0 to 5%).Symptoms varied by location and age. Localised eye swelling (20%, 95% CI 3% to 45%), cranial nerve deficits (14%, 95% CI 4% to 28%) and impaired visual function (6%, 95% CI 0 to 17%) were frequent in head and neck tumours. For abdomen/pelvic tumours, urinary symptoms (24%, 95% CI 5% to 15%), abdominal distension/discomfort (22%, 95% CI 4% to 47%), genital lump/swelling (16%, 95% CI 1% to 42%), constitutional symptoms (9%, 95% CI 0%] to 23%), vaginal bleeding (7%, 95%C I 0 to 21%) and bowel habit changes (6%, 95% CI 0 to 17%) were frequent.In <5 years, consumptive coagulopathy (16%, 95% CI 0 to 48%), cutaneous changes (5%, 95% CI 0 to 40%), genital lump/swelling (4%, 95% CI 0 to 14%), reduced mobility (3%, 95% CI 0 to 11%), vaginal bleeding (2%, 95% CI 0 to 11%) and bleeding/bruising/petechiae (2%, 95% CI 0 to 20%) were frequent compared with lump/swelling, constitutional symptoms, pain and headaches which were frequent among >11 years.
Conclusions:
For STS, pre-diagnostic symptoms differ by age and location, highlighting the need to tailor early diagnosis interventions.
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