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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
Further Reading


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