Prof Ivy A E Ekem 16 th September 2016 Blood enwikipediaorg M Komorniczak Accessed 080916 Development of blood cells enwikipediaorg Site of blood formation wwwhealthlinecomgtRef Library ID: 830227
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Slide1
Pointers to lymphoma and acute lymphoid leukaemia diagnosis
Prof Ivy A E
Ekem
16
th
September 2016
Slide2Blood
Slide3Slide4en.wikipedia.org / M.
Komorniczak
. Accessed 08.09.16
Slide5Development of blood cells
en.wikipedia.org
Slide6Site of blood formation
www.healthline.com>Ref Library
Slide7Peripheral blood and marrow
Slide8Slide9Outline
What lymphoma and acute lymphoid leukaemia are
Who they affect
How they present and why
How the diagnosis made
C
ardinal points in making diagnosis ----history, examination, selected investigations and their proper interpretation
Slide10What is lymphoma? What is acute lymphoid
leukaemia (ALL)?
Lymphoma – cancer of a white cell in the lymph nodes. Two broad groups:
Hodgkin lymphoma
Non-Hodgkin lymphoma e.g. DLBCL,
Burkitt
Acute lymphoid /
lymphoblastic leukaemia -
cancer of a
white cell in the marrow. Three subgroups:
L1
L2
L3 (
Burkitt
type)
Slide11Lymphoma
Affects lymph nodes;
the
spleen; thymus
gland.
Lymph nodes:
neck, armpits, groin, chest, abdomen and
pelvis.A
lymphoma develops when
an abnormal clone develops
Slide12Acute lymphoid leukaemia
Affects the bone marrow
Immature lymphoid cells called
lymphoblasts
appear
Proliferate rapidly to populate the bone marrow and blood
Depopulate the marrow of normal cells – red cells, normal white cells, platelets
‘Bone marrow failure’
Lymph nodes, spleen may also be affected
Slide13Same disease?
World Health Organization (WHO) classification of lymphoid
tumours
– listed together
Same cell, different stages of the cell at genetic change and type of change
Slide14Who they affect
All ages and sexes, but in lymphoma,
Hodgkin
lymphoma
bimodal peak, third and eighth decades
NHL
increases with age
In leukaemia
ALL
is more
common in childhood, especially
between 2
and 5
years of age.
Risk increases again
in people
aged 45 and above.
Slide15How they present and why
ALL
Bone marrow failure
Fever, night sweats
Enlarged lymph nodes
Lymphoma
Enlarged lymph nodes
Fever, night sweats
Unexplained weight loss
Slide16Why?
L
ymphoma
is the most common etiology of neoplastic fever of
unknown
origin.
The pathophysiology:
tumour necrosis factor and interleukins 1, 2, 4
Night sweats: body temperature regulation and circadian rhythm. Periodic
increases in interleukins (IL-1α, IL-2, IL-4, IL-6) and tumor
necrosis factor.
N
o research
found to support this
though.
Slide17How the diagnosis made
History, physical examination for both
Blood film and marrow for ALL
Lymph node / tissue biopsy for lymphoma
Other tests for further classification and staging
Slide18Cardinal points in making diagnosis: history
,
examination,
selected
investigations
and their proper
interpretation
History: Onset; suddenness in ALL. Swelling, systemic symptoms
examination: lymph node areas
Slide19Lymph node areas
www.healthresource4u.com
Slide20Case ‘stories’
Father insistence on marrow examination
B
one marrow trephine revealed diagnosis posthumous
B
one lesions in the young followed as for the elderly
Slide21Case 1: Father insists
A 14 year old previously well BECE candidate is admitted with unexplained fever and difficulty in walking of 2 weeks duration unto the medical ward.
Examination reveals a febrile young boy, well nourished and with
paraparesis
Slide22Investigations among others reveal a normal blood count
Marrow is requested (by father), not obliged (re…route of request).
Father insists a friend’s son presented similarly and was found to have leukaemia
Patient seen though, but on account of normal counts
……marrow not
done
Slide23Case 1 continued…..
Investigations continue for TB, viral illnesses etc.
LDH done
Presented at clinical meeting for leads to diagnosis
Bone marrow suggested and done on account of same history and high LDH
Diagnosis – Acute lymphoid leukaemia. Father was right.
Slide24Case 2: Posthumous diagnosis
51 year old man
Splenectomized
for
pancytopaenia
4 years earlier
Presented with febrile illness and severe joint pain
Managed for sepsis and rheumatoid arthritis…….improved
Pancytopaenia recurred when steroids were tapered
Slide25Some FBC results
Hb
– 8.1 g/dl; WBC - 3.66 x 10
9
/l with 85%L; Platelets – 63 x 10
9
/l
Hb
- 7.9 g/dl; WBC - 5.96 x 10
9
/l with 79.8L; Platelets – 111 x 10
9
/l
Hb
- 8.0 g/dl;
WBC
– 0. 88 x 10
9
/l with 93.6%L; Platelets – 34 x 10
9
/l
Slide26Case 2 ctd….
Hb
dropping
Trephine biopsy done
Read after patients demise
Diagnosis - ALL
Slide27Case 3: Bone lesions in the young
A young man, early 30s presented with features of a rapidly evolving debilitating illness
Amongst investigations, x-rays showed lytic lesions
Investigations continued as for myeloma….
More investigations revealed an LDH of over 2000U/L
?? Myeloma…. Patient demise
Post mortem: Lymphoma
Slide28A note on Lactate dehydrogenase (
LDH)
A
n enzyme
found in nearly all living cells (animals, plants, and prokaryotes).
Catalyzes
the
inter-conversion
of lactate to pyruvic
acid and so doing converts NAD
+
to NADH and back.
Raised levels in numerous medical conditions from
haemolysis
, through heart failure to malignancies however……
Slide29LDH ctd…
I
nvolved
in tumor initiation and metabolism
.
Cancer
cells rely on increased
glycolysis rather than aerobic respiration, thus
increased lactate production
This
allows
tumour
cells to convert the majority of their glucose stores into lactate
thus shifting
use of glucose metabolites from simple energy production to the promotion of accelerated cell growth and replication.
Slide30The unusual presenter
Listen. Follow every lead in the history. Retake history as often as necessary
Chase every result requested for. It must have been needed for it to have been requested. Consult the laboratory physician
Interpret results with patient in mind. Remember that every patient is unique in their signs and symptoms.
Slide31Take home messages for all of us
K
eep learning
Don’t take patient for granted
Lymphomas and acute lymphoid
leukaemias
can be difficult to diagnose but
good history taking,
efficient investigations and interpretation
W
ill give the diagnosis away in the great number of cases.