Paediatric Solid Tumors 2 Flashcards

(28 cards)

1
Q

Lymphomas are (benign or malignant?) proliferation of ____________ cells usually in association with lymphoid tissues (________,_________,___________)

A

malignant

lymphoid

lymph node, thymus, spleen

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2
Q

There are two main sub types;

__________ and _________-

A

Hodgkin’s and Non- Hodgkin’s

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3
Q

____________ lymphoma accounts for 50% of all lymphomas
Only 15% occur in children less than _____ years. (Common or Rare?) in under fives

A

Hodgkin’s

16; rare

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4
Q

Three distinct forms of Hodgkin lymphoma are seen from epidemiologic studies (childhood, young adult form & older adult form)
There is a (male or female?) preponderance in the childhood form

A

Male

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5
Q

Histological classification of classical
HL???

A

Nodular sclerosing
Mixed cellularity
Lymphocyte rich
Lymphocyte depleted

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6
Q

CLINICAL FEATURES of HL

Pain_____ indolent lymph node enlargement: Lymph nodes are initially ________ or ________, (tender or non-tender?) and (fixed or mobile?)

A

Painless

firm or rubbery

non-tender

mobile

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7
Q

Clinical features of HL

______________ is the commonest site. This makes diagnosis difficult. WHY?

_________________ is an uncommon presentation

Thirty percent of the children will present with the B symptoms
________ precedes lymphadenopathy in patients who manifest this

A

Cervical adenopathy is

Supraclavicular lymphadenopathy

Pruritus

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8
Q

DIFFERENTIAL DIAGNOSES of HL
1
2
3
Infectious mononucleosis
4 infection
Toxoplasmosis
5 infection
6
7
8

A

Tuberculous adenitis Bacterial adenitis
Viral cervical adenitis Infectious mononucleosis Cytomegalovirus infection Toxoplasmosis
HIV infection
Non Hodgkin’s lymphoma Rhabdomyosarcoma Neuroblastoma

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9
Q

List the B symptoms?

A

Fever
Night sweats
Weight loss

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10
Q

PROGNOSIS of HL

Overall survival is over _______% with over 75% of children alive after 20 years

Reduction in overall toxicity by reducing the _______________

Two-thirds of relapses occur within two years of treatment
5 Year event free survival for advanced disease ranges from 60 to 90%

A

90

Duration of chemo

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11
Q

NON-HODGKIN LYMPHOMA

They are a diverse group of cancers accounting for 5 – 10% of malignancies in children younger than 15 years
The incidence _____eases with age.
(Common or Rare?) in children less than 5 years

There is a (male or female?) preponderance

The disease is different between children and adults

A

incr; Rare

Male

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12
Q

All childhood NHLs are ________________

The risk of NHL is (more or less?) in immunocompromised children

A

rapidly proliferating

More

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13
Q

PATHOLOGY of NHL
They are histologically classified into four main groups
1) ______________ lymphoma
2) ______________ lymphoma (_______ & _________)
3) ___________ lymphoma
4) _________________ lymphoma

A

1)Lymphoblastic lymphoma
2) Small noncleaved cell lymphoma (Burkitt & Burkitt like)
3) Large B cell lymphoma
4) Anaplastic large cell lymphoma

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14
Q

Immunophenotyping

1)Lymphoblastic lymphoma
2) Small noncleaved cell lymphoma (Burkitt & Burkitt like)
3) Large B cell lymphoma
4) Anaplastic large cell lymphoma

A

Immature T cells
B cell
B cell
T cell/ Null cell

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15
Q

Clinical presentation

1)Lymphoblastic lymphoma
2) Small noncleaved cell lymphoma (Burkitt & Burkitt like)

A

Intrathoracic tumor, mediastinal mass

Intra-abdominal, jaw, endemic BL(70%), sporadic

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16
Q

Clinical presentation

3) Large B cell lymphoma
4) Anaplastic large cell lymphoma

A

ABDOMINAL TUMOUR

Lymphadenopathy, B symptoms

17
Q

COMPARISON OF ENDEMIC & SPORADIC BURKITT LYMPHOMA

Incidence
EBV association
Site of presentation

A

More; less

> 95%; >20%

Jaw, cns, orbit

Abdomen, marrow

18
Q

DIFFERENTIAL DIAGNOSES of NHL

ABDOMINAL
• _______blastoma
• ________blastoma
• ________oma
• Abdominal __________
•_____________

A

Nephro

Neuro

Rhabdomyosarc

Tuberculosis

Hodgkin’s lymphoma

19
Q

DIFFERENTIAL DIAGNOSES of NHL

JAW

•____________
• Ameloblastoma
• __________ ___________
• ______________
• _____________
•Dentigerous cyst

A

Osteomyelitis
• Hodgkin’s lymphoma
•Rhabdomyosarcoma
• Osteosarcoma

20
Q

RHABDOMYOSARCOMA

The peak incidence is between 2 to 5 years
Approximately 70% are diagnosed before the age of _________
(Males or Females?) are affected more than (males or females?)
It can occur in any part of the body

A

10 years

Males; females

21
Q

Rhabdomyosarcoma

It is classified based on pathologic features into
_________ (60%-80%)
___________(15%-20%)
____________ (8%)
_______________ (1%) & others(11%)

A

Embryonal

Alveolar

Undifferentiated

pleomorphic

22
Q

The most common soft tissue sarcoma in childhood is??

A

RHABDOMYOSARCOMA

23
Q

RETINOBLASTOMA
It is a ______________ malignancy of the _________ ____________ cells

A

neuroectodermal

embryonic retinal cells

24
Q

___________ is the most common intraocular tumour of childhood

A

Retinoblastoma

25
Retinoblastoma can be both heritable and non-heritable T/F
T
26
Retinoblastoma is due to ________________ of the ________________
Inactivation retinoblastoma gene
27
SYMPTOMS & SIGNS of retinoblastoma __________ (60%) ___________ of the eyes ______________ (20%) Pain____ red eye, hyphema (7%) ____________ (7%)
Leukocoria (60%) Asymmetry of the eyes Strabismus (20%) Painful red eye, hyphema (7%) Proptosis (7%)
28