Oncology 2 Flashcards

1
Q

What are lymphomas

A

Malignancies of the cells of the immune system

Hodgkin and NHL
NHL more common in childhood

Hodgkin is seen more in adolescence

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2
Q

Presentation of Hodgkin lymphoma

A

painless lymphadenopathy - most frequently in the neck

LN are very large and firm. May cause airway obstruction

Clinical history can be several months. Systemic symptoms uncommon..

B symptoms:
Sweating, pruritus, weight loss and fever

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3
Q

Investigations and management of Hodgkin’s lymphoma

A

LN biopsy
Radiological assessment of all nodal sites
Bone marrow biopsy
-Stage disease and determine treatment

combination chemotherapy with or without radiotherapy

PET scan to monitor treatment response

80% can be curedm 60% of disseminated disease

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4
Q

What is NHL

A

T-cell malignancy

B-cell malignancy

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5
Q

Presentation of NHL (T-cell malignancy)

A

Mediastinal mass with varying degress of bone marrow infiltration

May cause SVC obstruction

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6
Q

Presentation of NHL (B-cell malignancy - more commonly)

A

Localised LN disease, usually head and neck or abdomen

Abdo disease presents as pain from intestinal obstruction , a palpable mass or even intussusception in cases with involvement of the ileum

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7
Q

investigation and management in NHL

A

Biopsy, radiological assessment of all nodal sites (CT or MRI)
Examine bone marrow and CSF

Multi-agent chemo
80% survival rate for both T and B cell disease

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8
Q

Main differences between Hodgkins and NHL

A

Hodgkin’s lymphoma:

has Reed-Sternberg cells

Often starts in the upper body

Spreads very slowly and is very receptive to chemo and radiotherapy

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9
Q

When is chemo used.

Long-term complications of chemotherapy

A

Curative in ALL
Controls primary/metastatic disease in sarcoma/neuroblastoma
adjuvant treatment to deal with residual disease and to eliminate presumed micrometastases

Delayed puberty
Reduced fertility
Reduced growth
Neurotoxicity
Hepatotoxicity
Renal toxicity
Cardiotoxicity
Pulmonary toxicity
Secondary cancer
Psychological effects
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10
Q

Side effects of chemo

A
Hair loss
Anaemia
Infection
Bruising
Sore mouth
Nausea
Vomiting
Mood changes
Irritability
Weight gain
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11
Q

Long-term consequences of radiotherapy

A

Used for some tumours, but generally the risk of damage to growth and function of normal tissue is greater in a child

Also, babies are hard to immobilize

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12
Q

What are the forms of bone marrow transplant?

A

Allogeneic - from a compatible donor

Autologous - from patient, harvested beforehand while the bone marrow is uninvolved or in remission

Allogeneic usually in high-risk or relapsed leukaemia

Autologous usually used in solid tumours that have poor prognosis with conventional chemo (eg. advanced neuroblastoma)

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13
Q

What is a neuroblastoma

A

Arise from neural crest tissue in the adrenal medulla and sympathetic NS

Spontaneous regression sometimes occurs in very young infants

Spectrum from benign (ganglioneuroma) to highly malignant (neuroblastoma)

Most common before age of 5

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14
Q

Clinical features of neuroblastoma

A

Most children have an abdominal mass

Primary tumour can lie anywhere along the sympathetic chain from neck to pelvis.
Classically, adrenal primary.

At presentation, the tumour mass is often large and complex and can cross the midline and envelope major blood vessels and LN

paravertebral tumours may invade through the adjacent intervertebral foramen and cause spinal cord compression..

> 2 years, symptoms mostly from metastatic disease, particularly bone pain, bone marrow suppression causing weight loss and malaise.

Pallor
Weight loss
Abdominal mass
Hepatomegaly
Bone pain
Limp
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15
Q

Rarer clinical features of neuroblastoma

A
Paraplegia
Cervical lymphadenopathy
Proptosis
Periorbital bruising
Skin nodules
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16
Q

Investigations for neuroblastoma

A

Clinical and radiological features

Raised catecholamines

Confirmatory biopsy
Bone marrow sampling for metastases
MIBG scan with or without a DEXA scan

17
Q

Management of neuroblastoma

A

Metastatic disease is treated with chemotherapy
(including high-dose therapy with autologous stem cell rescue, surgery and radiotherapy)

Risk of relapse is high and the prospect of cure for children with metastatic disease is still little better than 30%

(retinoic acid) is now establishing a role in those with high-risk disease

18
Q

What is Wilm’s tumour

A

Originates from embryonal tissue

Commonest renal tumour of childhood

> 80% present before age of 5yrs

Rarely seen after 10 years of age

19
Q

Presentation of Wilm’s tumour

A

Large abdominal mass - often found incidentally

Uncommon features:
abdo pain
anorexia
anaemia (from haemorrhage into mass)
Haematuria
Hypertension
20
Q

Investigations in Wilm’s tumour

A

CT/MRI usually characteristic: intrinsic renal mass distorting the normal structure

Staging to assess metastases (usually lung) and initial tumour resectability plus contralateral kidney function

21
Q

Management of Wilm’s tumour

A

Chemo followed by delayed nephrectomy

Tumour is staged histologically which determines subsequent treatment. Radiotherapy is restricted to those with more advanced disease

more than 80% of all patients cured
Even with metastatic disease, prognosis is 60%.
Relapse carries poor prognosis.