solid tumours in childhood.pptwickup.weebly.com/uploads/1/0/3/6/10368008/solid_tumours_in... ·...
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SOLID TUMOURS IN CHILDHOOD
Fareed Omar
Paediatric Oncology
Steve Biko Academic hospital
Introduction
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Introduction
� Lymphomas and Leukemias make up about 40% of all childhood Cancers (Systemic cancers)
� 60% of childhood cancers are solid tumors
� About 40% of all solid tumors are CNS tumors
CNS tumours
� 25% of all childhood cancers (2nd most common after leukemia)
� Association with:
� Neurofibromatosis type I
� Tuberous Sclerosis
� Von Hippel-Lindau syndrome
� Supratentorial (40%) vs Infratentorial (60%)
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CNS tumours
� Supratentorial
� Glioma
� High grade
� Low grade
� Ependymoma
� PNET
� Craniopharyngioma
� Optic nerve glioma
� Infratentorial
� Cerebellum
� Medulloblastoma
� Astrocytoma
� Ependymoma
� Brain stem
� Glioma
� Other
Clinical
� Headache/irritability, vomiting
� Disturbance of gait and balance
� Hemiparesis/hemiplegia
� Cranial nerve abn: diplopia
� Mental disturbances
� Seizures
� Endocrine abnormalities
� Macrocephaly
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Hydrocephalus
Right cranial nerve VI palsy
Medulloblastoma (Infratentorial)
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Management
� Complete surgical resection if possible
� Multimodality treatment approach:
� Surgery
� Chemotherapy
� Radiotherapy
Neuroblastoma
� 7% of all childhood malignancies
� Peak age of incidence: 2 years
� Associated with:
� NF type I
� Hirschprung disease
� Turner syndrome
� Noonan syndrome
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Clinical
� Asymtomatic abdominal mass
� Adrenal mass most common
� Can arise anywhere along the sympathetic neural chain
� 50% - distant metastases at diagnosis
Anatomic site
� Head and neck: neck mass, horner’s syndrome
� Orbit and eyes – raccoon eyes
� Chest: dyspnea, pulm infections
� Abdomen
� Pelvis
� Paraspinal: dumbbell tumor
� Bone pain
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Other symptoms
� Sweating, flushing, pallor
� Hypertension
� Intractable watery diarrhea (kerner morrison syndr)
� Opsoclonus myoclonus ataxia syndrome (OMAS)
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Diagnosis
� CT scan
� Histology
� ↑Urinary levels of catecholamines: homovanillic acid (HVA) and vanillymandelic acid (VMA)
� I123-Meta-iodobenzylguanidine (MIBG) scintigraphy
� Bone scan
� Bone marrow aspirate
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Staging and Treatment
� International Neuroblastoma Staging system (INSS): stage 1- 4 and 4s
� Neoadjuvant chemotherapy followed by surgery and adjuvant chemotherapy ±radiotherapy
� Stage 4s: excellent prognosis even with no treatment
� Stage 4: very poor prognosis
Nephroblastoma (Wilms’ tumor)
� 6% of all childhood cancers
� Median age: 44 months (unilateral tumors) and 32 months (bilateral)
� Associated with:� WAGR syndrome (Wilms’, aniridia,
genitourinary malf, mental retardation)
� Denys-Drash Syndrome (Wilms’, renal failure and pseudohermaphroditism)
� Beckwith Wiedemann syndrome
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Beckwith Wiedemann syndrome
•Visceromegaly•Hemihypertrophy•Macroglossia•Abdominal wall defect•Microcephaly•Mental retardation hypoglycemia
Clinical
� Non-tender abdominal mass
� Microscopic hematuria
� hypertension
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Staging
� Stage I: completely resected with intact capsule
� Stage II: completely resected with penetration of capsule
� Stage III: Incompletely resected and or lymphnodes positive
� Stage IV: distant metastases
� Stage V: bilateral
Management and Prognosis
� Neo-adjuvant chemotherapy followed by surgery and adjuvant chemotherapy
� ± Radiotherapy
� Stage I: 98% 4yr OS
� Stage IV: 40%
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Retinoblastoma
� Mean age at diagnosis: 18 mo
� 40% of cases are hereditary – majority of these presenting with bilateral disease (15% of these have an established family history)
� 60% are non-hereditary mostly presenting with unilateral disease
Genetics
� Knudson’s two hit hypothesis – 2 events are required for tumour initiation:
� 1st –germline or somatic
� 2nd – somatic in individual retinoblast cells
� RB1 gene (tumour suppressor gene) mutation located on chromosome 13q14
� RB1 gene inherited as autosomal dominant
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Genetic counseling
� Unilateral / bilateral disease with + family history of RB:� 40% chance for sibling to get RB
� 40% chance of having offspring with RB
� Bilateral with – family history of RB� 6% chance for sibling to get RB
� 40% chance of having offspring with RB
� Unilateral with – family history of RB� 1% chance for sibling to get RB
� 8% chance of having offspring with RB
Clinical
� Leucocoria
� Strabismus
� Decreased visual acuity
� Inflamatory changes
� Hyphema
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Management
� If tumour small: local therapy:
� Brachytherapy
� Cryotherapy
� TTT (Transpupillary thermal therapy)
� Laser
� Chemotherapy
� Enucleation
� Combination of above esp for bilateral
Prognosis
� Stage I-II: Excellent >90% survival (maybe at the expense of losing the eye)
� Stage IV (CNS and or distant metastetic spread): <30% survival
� Very important to refer early
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Soft tissue sarcomas
� Rhabdomyosarcoma (RMS) vs non-rhabdomyosarcoma soft tissue sarcomas (NRSTS)
� 7% of all childhood malignancies
� Peak ages: 2-6 years
� Most sporadic
� RMS: alveolar vs embryonal subtypes
Rhabdomyosarcoma Clinical
� Can occur anywhere in the body – muscle
� <10yrs: head and neck or genitourinary areas
� >10yrs: extremity, trunk or para-testicular
� Presents as a painless mass/swelling, or due to compression of mass eg. urinary outflow obstruction
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Management
� Need to stage
� Neoadjuvant chemotherapy
� Complete surgical resection
� Adjuvant chemotherapy
� ±Radiotherapy
� Prognosis overall: >70% 5 yr survival (depending on stage)
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Bone tumours
� Osteosarcoma (56%) vs Ewing sarcoma (34%) (more prevalent in caucasians)
� 6% of all childhood cancers
� Peak incidence: 15 years (growth spurt)
� Very aggressive tumours
� Majority at presentation have metastases
Clinical
Usually incidental findingafter a history of minor trauma.
•Local pain/swelling•Decreased range of motion•Pathologic fracture
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Management
� Need to stage
� Usually metastases to skeleton, lungs
� Neo-adjuvant chemotherapy followed by surgery
� Limb-sparing surgery if possible
� Adjuvant chemotherapy
� Radiotherapy for Ewing sarcoma
� If metastetic at presentation: very poor prognosis
Other Solid tumours
� Germ cell tumours
� Hepatic tumours: hepatoblastoma and hepatocellular carcinoma
� Carcinomas: usually seen in adults and sometimes in adolescents
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Treatment of solid tumours
� Neo-adjuvant chemotherapy
� Surgery
� Adjuvant chemotherapy
� ±Radiotherapy
� Autologous stem cell transplant
Conclusion
� Early stage disease have excellent outcomes
� Therefore extremely important to refer early
� Stage IV disease: dismal outcome
� If in doubt: rather refer early and let us exclude cancer
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� Questions