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Chapter 102. Aplastic Anemia, Myelodysplasia, and Related Bone Marrow Failure Syndromes (Part 5) pdf

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Tiêu đề Aplastic anemia, myelodysplasia, and related bone marrow failure syndromes (part 5)
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Aplastic Anemia, Myelodysplasia, and Related Bone Marrow Failure Syndromes Part 5 Pathophysiology Bone marrow failure results from severe damage to the hematopoietic cell compartment.

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Chapter 102 Aplastic Anemia, Myelodysplasia, and Related Bone Marrow Failure Syndromes

(Part 5)

Pathophysiology

Bone marrow failure results from severe damage to the hematopoietic cell compartment In aplastic anemia, replacement of the bone marrow by fat is apparent in the morphology of the biopsy specimen (Fig 102-1) and MRI of the spine Cells bearing the CD34 antigen, a marker of early hematopoietic cells, are greatly diminished, and in functional studies, committed and primitive progenitor cells are virtually absent; in vitro assays have suggested that the stem cell pool is reduced to ≤1% of normal in severe disease at the time of presentation

Figure 102-1

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A Normal bone marrow biopsy B Normal bone marrow aspirate smear

The marrow is normally 30–70% cellular, and there is a heterogeneous mix of

myeloid, erythroid, and lymphoid cells C Aplastic anemia biopsy D Marrow

smear in aplastic anemia The marrow shows replacement of hematopoietic tissue

by fat and only residual stromal and lymphoid cells

An intrinsic stem cell defect exists for the constitutional aplastic anemias: cells from patients with Fanconi's anemia exhibit chromosome damage and death

on exposure to certain chemical agents Telomeres are short in a large proportion

of patients with aplastic anemia, and mutations in genes of the telomere repair

complex (TERC and TERT) can be identified in some adults with apparently

acquired marrow failure and without physical anomalies or typical family history

Aplastic anemia does not appear to result from defective stroma or growth factor production

Drug Injury

Extrinsic damage to the marrow follows massive physical or chemical insults such as high doses of radiation and toxic chemicals For the more common idiosyncratic reaction to modest doses of medical drugs, altered drug metabolism has been invoked as a likely mechanism The metabolic pathways of many drugs and chemicals, especially if they are polar and have limited water solubility,

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involve enzymatic degradation to highly reactive electrophilic compounds; these intermediates are toxic because of their propensity to bind to cellular macromolecules For example, derivative hydroquinones and quinolones are responsible for benzene-induced tissue injury Excessive generation of toxic intermediates or failure to detoxify the intermediates may be genetically determined and apparent only on specific drug challenge; the complexity and specificity of the pathways imply multiple susceptibility loci and would provide an explanation for the rarity of idiosyncratic drug reactions

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