Lymphadenopathy and Splenomegaly Flashcards

1
Q

Where is the hydrostatic pressure greater? At the arterial end or the venous end?

A
  • Arterial end
    • Hydrostatic pressure > Oncotic pressure
  • Venous end
    • Osmotic pressure > Hydrostatic pressure
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2
Q

Describe the lymphatic system.

A
  • Interstitial fluid is absorbed by lymph capillaries.
  • Lymph capillaries are thin-walled, endothelial tubes.
  • Avascular structures (epidermis, cornea, cartilage) do not have lymph vessels either.
  • Capillaries join and form lymph vessels.
  • Lymph in the vessels is filtered by lymph nodes.
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3
Q

Describe the structure of lymph vessels.

A
  • The lymph vessels, similar to veins, have valves inside of them.
  • Valves prevent retrograde flow of lymph.
  • A route for spread of disease:
    • Seed in the nodes
    • Distant metastasis - not a good sign for prognosis
  • ALWAYS examine the regional lymph nodes.
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4
Q

What is the sentinel lymph node?

A
  • The sentinel lymph node is the hypothetical first lymph node or group of nodes draining a cancer.
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5
Q

Describe the anatomy of the spleen.

A
  • Lymphoid organ below the left diaphragm,
  • Red pulp - sinuses lined by macrophages.
    • Receives red cells.
  • White pulp - similar to lymph node.
    • Receives plasma and white cells.
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6
Q

Describe the function of the spleen.

A
  • Red cell phagocytosis - e.g. old, damaged, antibody-coated cells removed.
  • Site of haematopoiesis in foetus and if ‘additional’ space is needed in adults.
  • Blood pooling - platelets > red cells.
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7
Q

What size are normal nodes?

What size are para-aortic or mediastinal nodes before they cause symptoms?

A
  • Normal nodes are up to 10mm (15mm in the groin) in short axis (imagine a kidney bean).
  • Normal nodes are easliy palpable in slim individuals (the worried well).
  • Internal nodes e.g. mediastinum or para-aortic are often 5-10cm before causing symptoms.
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8
Q

What are the red flags associated with lymphadenopathy?

A
  • Persistent lymph node or nodes for >6 weeks.
  • Firm, hard lymph node.
  • Lymph node >2cm in size.
  • Rapidly increasing in size.
  • Significant unintentional weight loss, night sweats, appetite loss.
  • Exposre to HIV or hepatitis.
  • Unexplained fever in a returning traveller.
  • Breast lumps or symptoms suggestive of common cancers.
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9
Q

Describe the surgical sieve.

A
  • Possible causes - MEDIC HAT PIN.
  • Metabolic - conditions relating to metbolism, biochemistry etc.
  • Endocrinological - conditions relating to various secretory systems.
  • Degenerative - conditions relating to age-related or stress-related destruction of tissue.
  • Inflammatory / infective - conditions that primarily present in a way that involves the profane activation of the immune system.
  • Congenital - conditions present from birth.
  • Haematological - conditions relating to the blood system.
  • Autoimmune - conditions relating to the inappropriate activation of the immune system.
  • Traumatic - conditions relating to a physical impact between two or more objects or environmental exposure.
  • Psychological - conditions related to a chemical imbalance or a disorder of thought process.
  • Idiopathic or iatrogenic - conditions without a known cause / caused by a doctor or resulting from treatment.
  • Neoplastic - conditions relating to cancers.
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10
Q

Describe the features of infective lymphadenopathy.

A
  • Regional response to infection - look for ‘red streak’.
  • Systemic infections, e.g. EBV / CMV / toxoplasma / HIV.
  • Nodes often tender / short history / variable size.
  • History / examination / passage of time / ?viral serology or PCR should help.
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11
Q

What diseases can cause inflammatory lymphadenopathy?

A
  • Local or systemic response to inflammation, e.g. eczema.
  • Auto-immune conditions e.g. rheumatoid arthritis or lupus.
  • Sarcoidosis (skin / lungs / lymph nodes).
  • Castleman’s disease (Human herpes virus-8 (HHV*) associated).
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12
Q

Describe the features of neoplastic lymphadenopathy.

A
  • Secondary
    • Existing malignancy or new diagnosis (latter e.g. melanoma / ENT / lungs).
    • Consider nodal drainage patterns.
    • Often hard, fixed nodes.
    • Fine needle aspiration (FNA) often useful.
    • Treatment plan depends on type and extent of tumour.
  • Primary lymphoproliferative disease
    • Often rubbery, mobile, non-tender nodes - local / systemic.
    • Check for ‘B symptoms’ - fever to 38°, drenching sweats, weigh loss >10% in <6 months.
    • FBC - ?chronic lymphocytic leukaemia.
    • Lactate dehydrogenase - non-specific marker of cell turnover.
    • FNA unhelpful, ?core or excision biopsy.
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13
Q

Give an overview of the staging of lymph node involvement in malignancy.

A
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14
Q

What factors are included in the prognostic index for Hodgkin’s disease?

A
  • Age
  • Stage
  • Hb
  • Albumin
  • Male
  • Lymphopenia
  • Low WBC
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15
Q

What factors are included in the prognostic index for Diffuse large B cell lymphoma (DLBCL)?

A
  • Age
  • Stage
  • LDH
  • Performance status
  • Number of extra-nodal sites
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16
Q

What factors are included in the prognostic index for follicular lymphoma (FL)?

A
  • Age
  • > 4 different sites
  • LDH
  • Hb
  • Stage 3 or 4
17
Q

What factors are included in the prognostic index for chronic lymphocytic leukaemia (CLL)?

A
  • Age
  • Stage (includes Hb / platelets)
  • β2 microglobulin
  • p53 mutation status
18
Q

What are the treatments for the diffrent types of neoplastic lymphadenopathy:

  • Hodgkin’s disease
  • Diffuse large B cell lymphoma
  • Follicular lymphoma
  • Chronic lymphocytic leukaemia
A
  • Treatment often adjusted by risk index and initial response e.g.:
    • Hodgkin’s disease and DLBCL - Short duration chemo- then radio- therapy for localised disease, extended or more intensive chemo for extensive disease.
    • Follicular lymphoma - radiotherapy for localised, ?watch and wait for asymptomatic disease.
    • CLL - watch and wait / chemo- and immunotherapy / targeted agents e.g. ibrutinib.
19
Q

What investigations are used to stage lymphoma?

A
  • Physical examination
  • CXR
  • CT
  • MRI if bone of CNS concerns
  • PET-CT (positron emission tomography) e.g. in Hodgkin’s disease or early stage DLBCL
20
Q

How do you quantify splenomegaly?

A
  • Spleen size relates to age and height.
  • 90% confidence interval of maximum spleen length by abdominal USS by height of the person.
21
Q

Describe the clinical examination of a patient with ?splenomegaly.

A
  • Normal size spleen can rarely be palpated.
  • Often needs to be 16-18cm pole to pole to be palpable.
  • Enlarges towards the right iliac fossa. Anterior structure so displaces bowel thus dull to percussion.
22
Q

What are the causes of splenomegaly?

A
  • Related to:
    • Function as a lymphoid organ
    • Function as reticulo-endothelial organ
    • Function as haematopoietic site
    • Related to anatomy of portal circulation
23
Q

What are the reasons for splenomegaly with respect to its lymphoid function?

A
  • Similar range as for lymph nodes.
  • Add malaria, schistosomiasis and other tropical causes.
  • Also Felty’s syndrome - splenomegaly with e.g. lupus or rheumatoid arthritis.
24
Q

What are the reasons for splenomegaly with respect to its function as a reticuloendothelial organ?

A
  • Site of RBC estruction so, any cause of haemolysis.
  • Storage disorders e.g. Gaucher disease.
  • Amyloid
25
Q

What are the reasons for splenomegaly with respect to its function as a haematopoietic site?

A
  • 20% of newborns have a palpable spleen before medulla of bone takes over.
  • Chronic myeloid leukaemia.
  • Myeloproliferative disorders e.g. primary polycythaemia, myelofibrosis.
26
Q

What are the reasons for splenomegaly with respect to its relation to the portal circulation?

A
  • Portal circulation - haemodynamic pressure.
    • Cirrhosis (hepatic)
    • Portan vein thrombosis (pre-hepatic)
    • Severe right heart failure (post-hepatic)
27
Q

How would you investigate splenomegaly?

A
  • History
  • Examination
  • Simple bloods
    • FBC
    • Reticulocytes
    • Blood film
    • Liver function
    • LDH
  • Imaging
  • ?? Bone marrow
  • ?? Splenic biopsy
28
Q

Describe the imaging of the spleen in splenomegaly.

A
  • USS
  • CT
  • Define:
    • size
    • focal changes
    • splenic vessels
    • associated pathology in nodes / liver etc.