neoplasim ii Flashcards

1
Q

Carcinoma > 90%
 Lymphoma
 Leukaemia
 Sarcoma
 Malignant Melanoma
 Rare Neoplasms
 Mixed Neoplasms (e.g. carcinosarcoma)
 Embryonic Neoplasms - Children
 Germ Cell Neoplasms - Testis and Ovary
 Glial Neoplasms - Brain
are all —- neoplasms

A

malignant ( check slide 4)

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2
Q

malignant tumour of epithelium is – which is invasive and curable if its in — stage

A

carcinoma
in situ

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3
Q

in situ carcinoma:
* No invasion beyond the —
* Basement membrane - separates epithelium from the underlying
tissue
* Cannot — adjacent tissue and not capable of — as they have no access to lymphatics or blood vessels
* Examples:
* Squamous cell carcinoma in situ of skin (Bowen disease)
* Ductal carcinoma in situ of breast (DCIS)
* Cervical intraepithelial neoplasia of uterine cervix (CIN)
* Invasive carcinoma
– Invades through — and is therefore capable of— through the vascular or lymphatic system

A

basement membrane
invade
metastasising
basement membrane
metastis
( check slide 8,9)

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4
Q

carinoma classification:
Classification based on the type of — from which the
tumour arises
 — cell carcinoma
 —
 — – well differentiated NE tumours (e.g.carcinoid) & neuroendocrine carcinoma (e.g. small cell)
 — carcinoma (transitional cell carcinoma)
 — cell carcinoma
 — carcinoma
 — carcinomas e.g. adenosquamous carcinoma

A

epithelium
squamous
adenocarcinoma
neuroendocrine
urothelial
basal
undifferentiated
mixed

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5
Q

clarification of lymphomas:
- lymph a is malignancy is — which includes — , — and –
hodgkin vs non hodgkin lymphoma:
- non hodgkin is — vs —-
- — vs —-

A

lymphocyte
b cells T cells n their precurosirs
T cell vs b cell
nodal vs extranodal

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6
Q

leukaemia is malignancy of — (myeloid, lymphoid, erythroid, megakaryocytic); present in – and circulate in the —
- its — vs —
- — vs —
- examples:

A

bone marrow cells
bone marrow
peripheral blood
acute vs chronic
amyloid vs lymphoblastic / lymphocytic
examples:
 Acute myeloid leukaemia
 Acute lymphoblastic leukaemia
 Chronic myeloid leukaemia
 Chronic lymphocytic leukaemia

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7
Q

—- tumours of mesychymal organs examples:
 Osteosarcoma ( — )
 Chondrosarcoma ( — )
 Angiosarcoma ( — )
 Liposarcoma ( —- )
 Leiomyosarcoma ( — )

A

sarcoma
bone
cartlige
blood vessel
adipose
smooth

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8
Q

clinical presentation of malignant neoplasm: ( clinically )
 Effect of —
 Effect of —
 Effect of — secretion
 — effects
 General effects of — disease

A

primary tumour
metastasis
hormone
paraneoplastic
malignant

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9
Q

clinical presentation of malignant neoplasm :
Effects of primary tumour:
1. — e.g. cancer of the breast
2. — e.g. colon
3. — - Haemoptysis
- Haematemesis
- Melaena
- P.R. bleeding
- P.V. bleeding
- Fe deficiency anaemia
4. — e.g. involving/infiltrating nerves, due to obstruction, etc.
4. Loss of — e.g. fracture of bone

A

mass forming
obstruction
bleeding
pain
function

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10
Q

effects of metastasis:
* — / — - e.g. axillary nodal mass
* — - e.g. of — due to a metastasis – signs of infection, shortness of breath (dyspnoea)
* — - e.g. —- due to lung metastasis
* Loss of — - e.g. — due to metastasis to brain, bone fracture, etc.
* —

A

lump / mass
obstruction
bronchus
bleeding
haemoptysis
function
stroke
ascites

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11
Q

effects of hormone secretion :
* ACTH secretion from — cell ca of lung causing —
* Parathyroid hormone related peptide (PTHrP) from — cell carcinoma of the lung causing —

A

crushing syndrome
small
squamous
hypercalacaemia

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12
Q

effects of paraneoplastic syndrome:

A
  • peripheral neuropathy
  • dermatomytositis
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13
Q

general effects of malignancy :
1- —-
2- —-
3- —

A
  • Weight loss / cachexia
  • Fatigue / lassitude
  • Anorexia – loss of appetite
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14
Q

diagnosis of malignancy:
1- —
2- —-
3- — test as:
– — tests: FBC, U&E, LFTs, tumour markers
– — : CT, MRI, PET
– — : FNA, Biopsy, Resection

A

clinical history
clinical examination
ancillary
blood
radiology
pathology
( check slide 23 ,24 , 25,28,31 )

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15
Q

squamous cell carcinoma occur at any area lined by —- as —

A

squamous epithelium
skin mouth oesophagus uterine cervix

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16
Q

squamous cell carcinoma :
- resemblacne to —
- —- production
- how do we know its sqaoumous :
* — on microscopy to assess likely biological behaviour
* Well differentiated
* Moderately differentiated
* Poorly differentiated

A

squamous cells
+/- keratin
grading

17
Q

adenocarcima have many different types and these occur in :
- the origin and resemblance to — or —
- — production
- —- formation
- grading :
* Well differentiated
* Moderately differentiated
* Poorly differentiated

A

– GIT
– BREAST
– THYROID
– UTERUS
– KIDNEY
glandular or columnar epithelium
+ mucin
+ granular

18
Q

small cell carcinoma usually arise in — but can occur at other sites
- high grade — carcinoma
- arises from —- ce;;s
- may be associated w — effects
- may be associated w — effects
* Sheets of small cells with
hyperchromatic nuclei,
inconspicuous nucleoli and
minimal cytoplasm, molding
of nuclei (nuclei indent one
another)
* Express neuroendocrine
proteins (detected by
immunohistochemical stains)
– Chromogranin-A,
Synaptophysin, CD56

A

lungs
neuroendocrine
neruendocrine cells
hormonal
paraneoplatic

19
Q

neuroendocrine tumours are:
– — -differentiated neuroendocrine tumours (in lung – carcinoid/atypical carcinoid nomenclature used)
– Neuroendocrine carcinoma (small cell carcinoma, large cell carcinoma)
Most – carcinoma biologically

A

well
aggressive

20
Q

urothelial carcinoma are – cell carcinoma
- these arise/ resembles —- aka — epithelium
- Normal urothelium lines
bladder, ureters, urethra and
renal pelvis
* In situ versus invasive
( Why is it necessary to know the type of carcinoma?
* Is it a primary tumour or a metastasis?
* Prognosis and treatment options may depend on the type of carcinoma.
Will the current method of neoplasm classification, based on morphology,
change in the future?
- Molecular analysis / personalised medicine)

A

transitional
urothelium