Neonatal Tumors
Neonatal Tumors
Key Points
- Incidence: 1-2 per 1000 live births
- Different biology from older children
- May be detected prenatally
- Unique management challenges
- Better overall prognosis than adult tumors
Special Considerations
- Unique Features
- Embryonic origin
- Rapid growth potential
- Different natural history
- Complex management decisions
- Diagnostic Challenges
- Limited radiation exposure
- Tissue sampling risks
- Complex differential diagnosis
- Need for specialized expertise
Classification & Types
Common Tumor Types
- Extracranial Teratomas
- Sacrococcygeal (most common)
- Cervical
- Mediastinal
- Retroperitoneal
- CNS Tumors
- Teratomas
- Astrocytomas
- Choroid plexus tumors
- Medulloblastomas
- Soft Tissue Tumors
- Infantile hemangiomas
- Fibrosarcomas
- Rhabdomyosarcomas
- Myofibromatosis
- Other Types
- Neuroblastoma
- Hepatic tumors
- Leukemia
- Renal tumors
Classification Systems
- By Origin
- Mesenchymal
- Neurogenic
- Germ cell
- Embryonal
- By Behavior
- Benign
- Borderline
- Malignant
Diagnostic Approach
Clinical Presentation
- Common Signs
- Visible mass
- Organ dysfunction
- Respiratory distress
- Feeding difficulties
- Associated Findings
- Hydrops fetalis
- Paraneoplastic syndromes
- Compression symptoms
- Constitutional symptoms
Imaging Studies
- Initial Evaluation
- Ultrasound
- Chest X-ray
- Limited CT/MRI
- Advanced Imaging
- Focused MRI protocols
- Nuclear medicine studies
- PET scan (selected cases)
Laboratory Studies
- Tumor Markers
- AFP
- β-hCG
- VMA/HVA
- NSE
- Basic Studies
- Complete blood count
- Liver function tests
- Coagulation profile
- Renal function
Treatment Principles
General Approach
- Initial Management
- Stabilization
- Supportive care
- Pain control
- Multidisciplinary planning
- Treatment Modalities
- Surgery
- Chemotherapy
- Observation (selected cases)
- Targeted therapy
Surgical Considerations
- Timing
- Emergency vs. elective
- Age-appropriate approach
- Organ preservation
- Technical Aspects
- Minimally invasive options
- Complete resection goals
- Reconstruction needs
Chemotherapy Principles
- Special Considerations
- Dose modifications
- Organ toxicity monitoring
- Growth/development impact
- Long-term effects
- Support Requirements
- Infection prophylaxis
- Nutrition support
- Growth factor support
Prognosis & Follow-up
Prognostic Factors
- Tumor-Related
- Histology type
- Stage/extent
- Molecular features
- Response to therapy
- Patient-Related
- Age at diagnosis
- Associated conditions
- Organ function
Follow-up Care
- Monitoring
- Growth/development
- Organ function
- Tumor markers
- Imaging surveillance
- Late Effects
- Endocrine function
- Neurocognitive development
- Secondary malignancies
- Quality of life
Specific Tumor Types
Sacrococcygeal Teratoma
- Features
- Most common neonatal tumor
- Female predominance
- Altman classification
- AFP monitoring essential
- Management
- Complete surgical resection
- Coccyx removal essential
- Chemotherapy for malignant elements
Neuroblastoma
- Characteristics
- Most common malignant tumor
- Adrenal origin common
- Stage 4S unique to infants
- Spontaneous regression possible
- Treatment
- Risk-stratified approach
- Observation for selected cases
- Surgery ± chemotherapy
Infantile Hemangioma
- Features
- Most common benign tumor
- Natural history of growth/involution
- PHACE syndrome association
- Management
- Observation vs. intervention
- Beta blockers first line
- Laser therapy role