Differentials

Wilms' tumour

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Haematuria.

Presence of congenital overgrowth syndrome (e.g., Beckwith-Wiedemann syndrome, Perlman syndrome, Sotos syndrome), or other syndrome such as Denys-Drash syndrome.

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CT or MRI abdomen/pelvis: renal mass with renal parenchyma stretching around the tumour (claw sign). Bilateral in 5% to 10% of cases.[46]

Ewing's sarcoma

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Typically occurs in adolescents or young adults.

INVESTIGATIONS

Bone x-ray: periosteal detachment from the bone (Codman's triangle); lesions typically arise from the diaphysis.

Biopsy: shows gene rearrangement and presence of fusion gene on fluorescence in situ hybridisation (FISH)/reverse transcription polymerase chain reaction (RT-PCR).[47]

Rhabdomyosarcoma

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

May present in a similar way to neuroblastoma.

Most common primary sites are the extremities and genitourinary system.

INVESTIGATIONS

Biopsy: FISH on biopsy sample shows PAX3-FOXO1 or PAX7-FOXO1 gene rearrangement for the alveolar subtype.[48]

Hepatoblastoma

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Presence of genetic syndrome associated with hepatoblastoma (e.g., familial adenomatous polyposis, Beckwith-Wiedemann syndrome, Li-Fraumeni syndrome, trisomy 18, and glycogen storage disease types I, III, IV).[49]

INVESTIGATIONS

Serum alpha-fetoprotein level: elevated.

CT or MRI abdomen/pelvis: hepatic mass.

Leukaemia

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Fever (rare in patients with neuroblastoma).

Hepatosplenomegaly.

INVESTIGATIONS

FBC: typically shows pancytopenia; may also show leukocytosis.

Peripheral blood smear: leukaemic lymphoblasts typically seen in acute lymphoblastic leukaemia.[50]

Bone marrow aspiration/biopsy: hypercellularity and infiltration, as well as other typical findings depending on the type of leukemia.

Hodgkin's lymphoma

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Typically occurs in adolescents or young adults.

Lymphadenopathy.

Presence of B symptoms (i.e., weight loss, night sweats, unexplained fevers).

May have co-existing autoimmune disorder.

INVESTIGATIONS

Lymph node biopsy: presence of Reed-Sternberg cells.[51]

Adrenal haemorrhage

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

May occur in neonates as a result of delivery trauma, infection, or other causes.

Signs of adrenal insufficiency may be present.

INVESTIGATIONS

Ultrasound: shows adrenal haematoma.[52]

Rapid improvement over several weeks on serial ultrasounds.

Other adrenal tumours

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Adrenal cortical carcinoma or other primary adrenal/renal masses are extremely rare in this young population.

INVESTIGATIONS

Imaging and biopsy: confirm presence and type of tumour.

Other causes of opsoclonus-myoclonus ataxia (OMA)

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

May occur in neuroblastoma, but may also be associated with hepatitis C, Lyme disease, Epstein-Barr virus, and streptococcus infection.[53][54][55][56] [57]

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Diagnosis is clinical.

Infections

SIGNS / SYMPTOMS
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SIGNS / SYMPTOMS

Rash may be present.

Fever.

INVESTIGATIONS

Blood culture: typically shows the causative bacterial organism.

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