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