Speciality 09 · Paediatric Surgical Oncology

Gentle words for children. Steady plans for the parents holding them.

Nothing prepares a family for this diagnosis — not love, not faith, not research at midnight. What helps is a plan: child-sized explanations, chemotherapy-first protocols when they improve outcomes, surgery timed around growth, and parents kept inside every decision.

Chemo -first protocols Parent at anaesthesia where possible Growth -aware surgery School reintegration focus
Understanding

Childhood cancer is its own world

Children do not get small versions of adult cancers — they get their own diseases entirely: Wilms’ tumour of the kidney, neuroblastoma, rhabdomyosarcoma, hepatoblastoma of the liver, teratomas and sacrococcygeal tumours, and childhood soft-tissue masses. Each follows established international protocols, and each responds better to protocol than to improvisation.

Surgery is performed in coordination with paediatric oncology teams — because in children, the sequence matters as much as the operation. Shrinking a tumour with chemotherapy first can turn a dangerous removal into a safe one. Timing operations around growth plates protects height, posture and organ development for decades ahead.

And the child’s experience counts as an outcome in itself: explanations in age-appropriate language, a parent present at anaesthesia wherever possible, honesty that never becomes frightening. Children sense truth even when it isn’t spoken — our job is to make the truth bearable.

For parents and grandparents

Signs children can’t tell us about

Almost all of these will have ordinary causes. But when one persists, a simple examination settles it — and childhood cancers reward early discovery like few others.

  • A tummy growing or looking unevenly swollen, beyond normal toddler roundness.
  • A new lump anywhere — neck, armpit, groin, limb.
  • Limping without a fall to explain it.
  • Refusing to stand or walk, especially after days of vague fussiness.
  • Bruising in odd places — trunk, back — not matching play.
  • Tiredness that rest doesn’t fix, fading from games they loved.
  • A white reflection in the pupil, often noticed first in camera flash photographs.
  • Weight loss or slipping off the growth chart despite eating normally.
Scope of care

Tumours we treat

The commonest solid tumours of childhood — each with established, evidence-backed protocols.

Wilms’ Tumour

Kidney tumours of early childhood with some of the best cure rates in oncology.

Neuroblastoma

Adrenal and nerve-chain tumours staged carefully and treated by risk group.

Rhabdomyosarcoma

Muscle-origin tumours managed within combined chemotherapy-surgery protocols.

Hepatoblastoma

Liver tumours of infancy, often made operable by chemo-first shrinking.

Teratomas & Sacrococcygeal

Congenital tumours removed with growth and future function protected.

Soft-Tissue Masses

Any persistent childhood lump investigated properly before anyone calls it harmless.

Our approach

What makes care here different

  • Chemo-first protocols when appropriateShrinking tumours before surgery makes operations smaller, safer and kinder.
  • Parent present at anaesthesiaWherever safely possible, no child drifts off alone — and wakes to familiar faces.
  • Growth-aware surgeryIncisions and resections planned so growing bodies keep their architecture.
  • Child-life friendly explanationsThe tumour described honestly but gently, in words your child can hold.
  • Coordinated paediatric oncology teamsChemotherapy, radiology and pathology speaking the same protocol language.
  • School-reintegration focusRecovery measured in return-to-normal milestones — classrooms included.
Your child’s pathway

From first visit to back-to-school

  1. A calm first meeting

    Reports reviewed personally while your child plays in the room.

  2. Staging scans

    Imaging arranged quickly, explained to you before your child sees anything.

  3. Team conference

    Paediatric oncology plans the full sequence — not just the operation.

  4. Protocol treatment

    Chemotherapy first when protocols say so; surgery timed for maximum safety.

  5. Surgery & recovery

    Growth-aware operation, parents close throughout, updates daily.

  6. Back to life

    Surveillance on schedule — and a deliberate plan for returning to school.

Honest answers

Parents usually ask…

Because shrinking first changes what surgery has to do. A Wilms’ tumour reduced by half is removed through a smaller incision with less risk of spillage; a hepatoblastoma once deemed unresectable often becomes removable entirely. Protocols order treatments by evidence of benefit — not by tradition.

Among the highest in all of cancer medicine — overall survival exceeds ninety percent in modern protocols, including many children with advanced disease at diagnosis. Hearing that number honestly, early, is part of treatment too: this is a fight families win far more often than not.

This is engineered against deliberately. Surgery avoids growth plates where possible; radiation doses and fields are planned around developing bones and organs; long-term follow-up watches height, hormones and development through adolescence. Some effects can occur — which is precisely why surveillance continues into adulthood.

In age-appropriate truth: younger children need to know the tummy lump is making them ill and that doctors and mummy-papa will fix it together; older children deserve the word cancer and honest reassurance about what treatment means day-to-day. Child-life specialists help you script it — children cope better than we fear when told gently and consistently.

Yes — presence is treated as medicine here. A parent accompanies the child into anaesthesia where facilities allow, stays during ward rounds, and receives updates directly. Recovery plans are built assuming you will be there, not working around you.

Call 🗓 Book 💬 WhatsApp