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8/13/2019 Sgpath Case01 Dir
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Case 1
Stephan Dirnhofer and Andr Tichelli
40-years old man, admitted for thoracic pain
Diagnosis of classical Hodgkin lymphoma, nodular
sclerosis, in a cervical lymph node
Bone marrow biopsy for lymphoma staging
History / Clinical findings
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Blood counts
x109/L150-400198198Platelets
x109/L3.5-10.512.212.2WBC
fL80-958888MCV
g/L140-160142142Hemoglobin
UnitsReferenceResultParameter
Peripheral blood
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Cytology bone marrow
Indications
for bone marrow examination Investigation of peripheral blood abnormality
- cytopenias, cytosis, abnormal cells
Selected types of infectious diseases- Parvo-virus B19, Leishmaniosis, others
Fever of unknown origin, unexplained splenomegalie, storage disease
Staging and management of tumor patients- all lymphomas, childhood neoplasms, others
Plasma cell dyscrasias incl. amyloidosis
Systemic mast cell disease
Monitoring of patients with leukemia
- response to therapy, stem cell transplantation Miscellaneous
- hps, effectsof therapy, immunodeficiency, bone disorders
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Strength of bone marrow biopsy
Assessment of:! cellularity, topographical distribution of hemopoesis
and inter-relationships of cells
! bone structure, blood vessels, stroma, lymphoid
aggregates, iron content and degree of fibrosis or
necrosis
! focal processes (carcinoma, lymphoma, granuloma
and other infiltrative processes)! bone marrow infiltration pattern for lymphomas,
mast cell disease and others
Additional investigations (IHC, FISH, PCR)
Strength of bone marrow cytology
Individual cell morphology, dysplastic changes of the
erythropoiesis and myelopoiesis, Auer rods in the blasts
Particular forms of AML recognizable: Promyelocyticleukemia, AML with t(8;21), AML M4eo with t(16) or
inv(16)
Ringed sideroblasts for sideroachresia
Material for flow-cytometry, cytogenetics and molecular
genetics
Rapidly available for analysis (1-2 hours)
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Algorhytm for BM-biopsies
See the biopsy with a smear (and a hematologist)
Systematic assessement of:
Cellularity, Bone structure
Topography and Maturation of all three cell lines
Dysplasia, Blasts
Lymphocytes, Plasma cells, other infiltrates
Iron, Fibers
Others: Granulomas, Mast cells, (Pseudo-)Gaucher cells...
Final interpretation is an integrative diagnosis: a morphological
diagnosis in combination with hemogramm, laboratory data,
genetics and clinical findings
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H&E
H&E
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Gm
Final diagnosis
Normocellular, completely maturing
bone marrow
No evidence of Hodgkin Lymphoma
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A normal bone marrow contains
1. No blast at all
2. Between 1-4% blasts
3. !5% blasts
4. No blasts but >5% CD35+ cells
(exclusively endothelial cells)
5. Any number but always CD34-
negative
A normal bone marrow contains
1. No blast at all
2. Between 1-4% blasts3. !5% blasts
4. No blasts but >5% CD35+ cells
(exclusiveley endothelial cells)
5. Any number but always CD34-
negative
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Among the following, what is
the strength of marrow biopsy
1. Assess dysplasia of myelopoiesis
2. Assess ringed sideroblasts
3. Recognize Hodgkin infiltration
4. Point 3 and 5
5. Assess topographical distribution ofthe cells
Among the following, what is
the strength of marrow biopsy
1. Assess dysplasia of myelopoiesis
2. Assess ringed sideroblasts
3. Recognize Hodgkin infiltration
4. Point 3 and 5
5. Assess topographical distribution of
the cells
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Among the following, what is the
strength of marrow cytology
1. Assess diagnosis of acute
promyelocytic leukemia
2. Assess fibrosis in CIMF
3. Recognize granulomas
4. Point 3 and 55. Recognize infiltration of carcinoma
Among the following, what is the
strength of marrow cytology
1. Assess diagnosis of acute
promyelocytic leukemia2. Assess fibrosis in CIMF
3. Recognize granulomas
4. Point 3 and 5
5. Recognize infiltration of carcinoma
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Take home messages
Use standardized diagnostic approach Consider clinical findings including blood
counts and differentials
Consider peripheral blood smear and
aspirate
Consider flow cytometry, genetics and
stem cell cultures
Integrate all data for final diagnosis
Well, ...it looks like
you broke the
Jamishidi-needle
...
Clinico-pathological cooperation is essential