The RES Flashcards

1
Q

Anatomy of the neck lymph glands

A
  • anterior cervical chain
  • submandibular
  • submental
  • pre auricular
  • post auricular
  • occipital
  • supra clavicular nodes
  • run along the anterior aspect of the trap muscles.
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2
Q

recall the lymphatic system *thoracic duct

A

inserts itself into the brachiocephalic trunk

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3
Q

lymph node anatomy

A

size of a little finger nail
shaped like a bake bean
will be reported from the shortest axis (middle)

lymph nodes communicate with each other. flows out through hilum. blood vessel feeds in

what comes in: naive cells from the bone marrow and will be switched on/dampened/amplified. e.g. a B cell coming in and expresses the antibody. then there is a linkage chain (HLA) and any self antibodies will get deleted. if the linkage does not work properly- auto imminity.

(lymph nodes goes up to it, tells it what it’s going to delete and gets deleted if it’s auto reated)

can get EXPANDED in the secondary folliclce

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4
Q

Secondary follicle segment?

A

cortex= predominantly where B cells are

get amplified (secondary follicles will expand) = that’s why you get enlarged lymph nodes. capsules stretch

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5
Q

Secondary follicle segment?

A
  1. cortex= predominantly where B cells are

get amplified (secondary follicles are expanding) = that’s why you get enlarged lymph nodes. capsules stretch. if it happens slowly, the capsule can stretch slowly too. rapid expansion can be uncomftorble (infection, malignancy, rapidly growing aggressive non-hodgkin lymphoma infiltrating)

  1. paracortical area: contains T cells.
  2. medullary core: contains macrophages and plasma cells (antibody producing T cells)
  3. fat
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6
Q

the spleen

A

the biggest lymph node we have

sits in the L hypochondrium.
covered by the ribs

dimensions
5 inches (12.5 cm) in long anxis
1 x 3 x 5 x 7 x 9 x 11
1/3 superior part
2/3 bottom part

spleen has to be very big to be able to feel it
*examination

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7
Q

anatomy of the spleen

A

red pulp= highly vascular part to the spleen. thick capsule.
*tiny venous lakes that will accumulate in the blood
RBC come here to be removed (e.g. mishapen / target cell)

white pulp
*primary and secondary follicles

? macrophages will bite off a bit of the RBC which will have a bit of RNA- removal.

capsulated organisms
meningococcus / pneumococcus
immunological function provided by the spleen is critical to fight capsulated organisms.

if no spleen - give penicillin.

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8
Q

anatomy of the spleen

A

red pulp= highly vascular part to the spleen. thick capsule.
*tiny venous lakes that will accumulate in the blood
RBC come here to be removed (e.g. mishapen / target cell)

white pulp
*primary and secondary follicles

? macrophages will bite off a bit of the RBC which will have a bit of RNA- removal.

capsulated organisms
meningococcus / pneumococcus
immunological function provided by the spleen is critical to fight capsulated organisms.

if no spleen (hyposplenia= if you have coeliac you can have a dysfunction spleen) - give penicillin.. people with sickle cell should be on penicillin their whole life.

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9
Q

lymphomas

A

name according to the cell it originated from (e.g follicular lymphoma)

mantel cell lymphoma from the mantel zone

proliferation of the lymphatic structure
early-
- follicular lymphoma
- mantel cell lymphoma
- plasma cells
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10
Q

T cell lymphoma

A

sometimes just localised to the skin (outside of the skin is very bad)

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11
Q

B cell lymphoma

A

non hodgkin lymphoma (B cell)

hodgkin lymphoma
(mixture of everything, not just B cells) reed-sternerg cell, owl

age= 25-30 y/o
second peak= 60 y/o

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12
Q

B cell non hodgkin lymphoma

A

1) indolent

2) aggressive

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13
Q

B cell non-hodgkin lymphoma

A

1) indolent
2) aggressive (rapidly proliferative + constitutional symptoms)
* measure the LDH

mx: chemotherapy (radiotherapy can be treated for residual/local lymphomas. hodgkin lymphoma with a mediastinal mass)

RT can cause myelodysplasia / AML in later years.

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14
Q

chemotherapy for B NHL

A
RCHOP
ritoximab *MOA
cyclophosphomadie
hydroxyrubacin
oncovin (finapristine?)
prednisolone

steroids side effects= weight gain.

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15
Q

normal lymphocyte development

A

look up autoimmunity ….

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16
Q

description of a lump

A

Size –width / height / depth
Site/Location– anterior triangle / posterior triangle / mid-line
Shape – Ovoid, round
Skin changes– erythema / ulceration/punctum

Consistency– smooth / rubbery / hard / nodular / irregular
Contour or Surface
Trans-illumination– suggests mass is fluid-filled (i.e. cystic hygroma)
Temperature– increased warmth may suggest an inflammatory or infective cause

Fluctuance– if fluctuant, this suggests it is a fluid-filled lesion (i.e. cyst)
Pulsatility– suggests vascular origin (i.e. carotid body tumour/aneurysm)
Relation to underlying/overlying tissue– tethering/mobility (ask the patient to turn their head)
Auscultation– to assess for bruits (i.e. carotid artery aneurysm)

17
Q

causes of splenomegaly

A

The Big 3:
Myeloproliferative: Myelofibrosis, PRV, ET (rarely), MPN/MDS overlap. CML at presentation or relapse
Lymphoproliferative: Lymphomas, CLL etc
Portal hypertension: From a variety of causes; and in chronic/severe heart failure

Rest of the World: Infection is number 1: EBV, CMV, HIV, Malaria, TB, Visceral Leishmaniasis, Endocarditis, hydatid disease, Typhoid.

Haemolytic anaemias: Congenital such as HS, PK deficiency, Sickle cell disease (splenic sequestration). Acquired haemolytic anaemia
Thalassaemias: Transfusion dependent beta-Thal, HbH disease
Other autoimmune diseases: SLE, RA (Felty’s)
Infiltrative diseases: Gauchers, Amyloidosis, Sarcoid, Cancer, Neimann-Pick
Splenic vein thrombosis, Haemangiomas
Subcapsular haematomas (without rupture