bone marrow class

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Bone marrow Anatomy, Functions, Aspiration & Reporting Dr. Narender Kumar

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Page 1: Bone marrow class

Bone marrowAnatomy, Functions, Aspiration & Reporting

Dr. Narender Kumar

Page 2: Bone marrow class

Anatomy..

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•Two types of bone marrow: ▫Medulla ossium rubra (Red Marrow -

consisting mainly of hematopoietic tissue)▫ Medulla ossium flava (Yellow Marrow -

consisting mainly of fat cells)

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•  On average, bone marrow constitutes 4% of the total body mass of humans

• In adults weighing 65 kg (143 lbs), bone marrow accounts for approximately 2.6 kg (5.7 lbs)

• The hematopoeitic compartment of bone marrow produces approximately 500 billion blood cells per day

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Primitive Hematopoiesis

• Derived from the extra- embryonic YOLK SAC;

• Consists mainly of nucleated erythroid cells that carry oxygen to the developing embryonic tissues… an early circulatory system.

• Probably starts ~ 4 weeks in humans

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Subsequent sites of Hematopoiesis in fetal life

• Throughout fetal life, the liver is the chief organ for production of myeloid and erythroid cells

After birth, BONE MARROW becomes main hematopoietic organ.

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Pattern of distribution..• At birth, all bone marrow is red. • With age, more and more of it is

converted to the yellow type; only around half of adult bone marrow is red

• In Adults Red marrow is found mainly in the Flat bones and in the   epiphyseal ends of long bones such as the femur and humerus

• Yellow marrow is found in the medullary cavity, the hollow interior of the middle portion of long bones

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Bone Marrow• Bone marrow is specially designed to support the

proliferation, differentiation, and maintenance of hematopoietic cells

• The stroma of the bone marrow is all tissue not directly involved in the primary function of hematopoiesis.

• Cells that constitute the bone marrow stroma are:• fibroblasts (reticular connective tissue)• macrophages• adipocytes• osteoblasts• osteoclasts• endothelial cells, which form the sinusoids.

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• Bone marrow examination refers to the pathologic analysis of samples of bone marrow obtained by bone marrow aspiration and bone marrow biopsy (often called a trephine biopsy)

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•  The aspirate yields semi-liquid bone marrow, which can be examined • under a light microscope as well as• analyzed by flow cytometry,•  chromosome analysis, or•  polymerase chain reaction (PCR).

• Frequently, a trephine biopsy is also obtained, which yields a narrow, cylindrically shaped solid piece of bone marrow which is examined microscopically (sometimes with the aid of immunohistochemistry) for cellularity and infiltrative processes.

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How the test is performed…

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How the test is performed…• usually performed on the

back of the hipbone, or posterior iliac crest.

• However, an aspirate can also be obtained from the sternum (breastbone).

• A trephine biopsy should never be performed on the sternum, however, due to the risk of injury to blood vessels, lungs or the heart.

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• Sahla Bone Marrow Needle, iliac crest, with adjustable stop

• 14 (2.0mm) x 50mm• 16 (1.6mm) x 50mm• 18 (1.2mm) x 50mm (in child)

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Contraindications

• The only absolute reason to avoid is the presence of a severe bleeding disorder

Complications

• While mild soreness lasting 12-24 hours is common after a bone marrow examination, serious complications are extremely rare.

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Erythroid seriesMyeloid seriesMegakaryocytic seriesMonocytic series

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*Proerythroblast**Early erythroblast (Basophillic )***Intermediate erythroblast (Polychromatic)****Late erythroblast (Orthochromatic )

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Erythroid precursors

• Normal red cells are produced in the bone marrow from erythroid precursors or erythroblasts.

• The earliest morphologically recognisable red cell precursor is derived from an erythroid progenitor cell which in turn is derived from a multipotent haemopoietic progenitor cell.

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proerythroblast• Normal

proerythroblast [dark red arrow] in the bone marrow. This is a large cell with a round nucleus and a finely stippled chromatin pattern. Nucleoli are sometimes apparent.

• The cytoplasm is moderately to strongly basophilic.

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Basophilic erythroblast

• Spherical nucleus, nucleoli not visible, basophilic cytoplasm

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Polychromatophilic erythroblast• smaller nucleus –

condensed chromatin, baso- and eosinophilia in the cytoplasm

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Orthochromatophilic erythroblast • small nucleus with highly

condensed chromatin, nucleus extruded, eosinophilic cytoplasm

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Normal erythroblasts in the BM

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Myeloid precursors

•Myeloblast promyelocyte myelocyte metamyelocyte band form mature neutrophil.

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credit-Dr. Lekstrom Hines, J EM 1999

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Normal granulocyte precursors in the bone marrow

• Note the myeloblast [dark red arrow] with a high nucleocytoplasmic ratio, diffuse chromatin pattern and nucleolus.

• There is a promyelocyte [green arrow] which is larger and has a lower nucleocytoplasmic ratio and abundant azurophilic granules.

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Myelocytes • Myelocytes are

smaller than promyelocytes and have specific granules that indicate whether they are of neutrophil, eosinophil or basophil lineage.

• The nucleolus is no longer visible.

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Eosinophilic myelocyte

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A neutrophil metamyelocyte•The metamyelocyte

differs from a myelocyte in having some indentation of the nucleus

• It differs from a band form in not having any part of its nucleus with two parallel edges

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Neutrophilic metamyelocyte

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Eosinophilic metamyelocyte

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Basophilic metamyelocyte

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Band or juvenile Neutrophils

•There are smaller numbers of cells of neutrophil lineage with non-segmented nuclei. They are referred to as neutrophil band cells or band forms. They are less mature than segmented neutrophils.

.

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Compare the different cell types:

basophilic (myeloid) eosinophilic (myeloid)

neutrophilic (myeloid) erythroid

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*Megakaryoblasts** Promegakaryocytes***Megakaryocytes

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Megakaryoblasts

•Megakaryoblasts are the precursors of the megakarycytes.

•They may show cytoplasmic blebbing.

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Promegakaryocyte

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Megakaryocyte

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Monocytopoiesis

- Monoblast

- Promonocyte

- Monocyte

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Promonocyte

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19-49

Hematopoiesis

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Systemic scheme for Examining aspirated BM films•Low power (x10)

▫Determine cellularity▫Identify megakaryocytes▫Look for clumps of abnormal cells▫Identify macrophages

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Systemic scheme for Examining aspirated BM films•Higher power (x40, x100)

▫Identify all stages of maturation of myeloid and erythroid cells.

▫Determine the M:E ratio▫Perform a differential count▫Look for areas of BM necrosis.▫Assess the iron content.

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Assessment of BM cellularity

• Cellularity cannot be assessed without knowing the age of a patient.

• A young child on average has about 80% of the intertrabecular space occupied by haemopoietic cells whereas in a 75-year-old the average has fallen to around 30%.

•100 – Age of Patient

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Comparing normo, hyper, & hypocellular marrows

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M:E ratio•The M:E ratio is the ratio of all granulocytic

plus monocytic cells (Myeloid) to all erythroblasts (Erythroid).

•For all bone marrow aspirates examined, the report should specify the M:E ratio and the percentage of lymphocytes and plasma cells.

•A differential count of at least 200-300 cells should be performed.

•If there is any borderline abnormality, e.g. in the number of blasts, lymphocytes or plasma cells, a 500 cell differential count should be performed.

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•Only after the bone marrow has been carefully assessed on low and medium power the X100 oil should be used to assess cellular detail

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BM iron stores• Once all normal and

abnormal bone marrow cells have been assessed on a routine stain an iron stain should be examined, using a medium power objective (X 40 or X 50). Storage iron, which stains blue, should be assessed in bone marrow fragments. This image shows normal bone marrow iron.

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Reporting results

• List the various descriptive comments regarding all the cell lines present in the BM

•Mention the striking abnormalities separately.

•Write your impression and any recommendations to the clinician.

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Cellular constitution of the red bone marrow parenchyma

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Trephine biopsy

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• Jamshidi Type Bone Marrow Biopsy Needle, • 8swg (4.0mm) x 100mm• 11swg (3.0mm) x 100mm• 13swg (2.3mm) x 90mm• 14swg (2.0mm) x 90mm (In child)

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Adequacy of biopsy

•should contain at least five to six intertrabecular spaces and, after processing,

•should be at least 2–3 cm in length• Others have considered that 1.5–2 cm is

an acceptable length

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Indications or areas of controversy•Inadequate or failed aspirate.•Need for accurate assessment of cellularity,

whether increased or decreased.•Suspected focal lesion (for example,

suspected granulomatous disease or lymphoma).

• Suspected bone marrow fibrosis.• Need to study bone marrow architecture.• Need to study bone structure or bone

marrow blood vessels

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