Difference between revisions of "Myelodysplastic syndromes"

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#*Congenital hematopoietic disorder.
#*Congenital hematopoietic disorder.
#**Congenital dyserythropoietic anemia.
#**Congenital dyserythropoietic anemia.
=Bone marrow specimens=
==Normal==
*Age (years) ~ percentage of fat.
**Example 80 years old has ~ 80% fat in marrow space.
Erythroblasts:
*Typically away from bone.
Megakaryocytes:
#Alone - not in clusters.
#Not close to bone.
Myeloid cells:
*Adjacent to bone.


=Histologic features=
=Histologic features=
Line 103: Line 120:
*Non-lobated nuclei of any size.
*Non-lobated nuclei of any size.
*Multiple widely separated nuclear lobes.
*Multiple widely separated nuclear lobes.


=See also=
=See also=

Revision as of 16:50, 29 May 2011

Myelodysplastic syndromes, abbreviated MDS, can be thought of a pre-leukemia/pre-lymphoma.

They should not be confused with myeloproliferative neoplasms.

Overview

Lab fidnings

  • +/-Anemia.
  • +/-Neutropenia.
  • +/-Thrombocytopenia.

Notes:

  • MDS is usu. an incidental finding, i.e. it is asymptomatic.

Associations

Syndromes associated with MDS:[1]

  • Fanconi syndrome.
  • Diamond-blackfan syndrome.
  • Shwachman-diamond syndrome.

Diagnostic criteria

All of the following:[1]

  1. At least 6 months + persistent.
  2. Dysplasia.
    • Cytologic:
      • Need >=10% abnormal.
    • Cytogenetic.
  3. All other causes excluded.
  4. Blast percentage <20%.
    • If >=20% = leukemia.
    • Criteria blast percentage:
      • Bone marrow: 500 nucleated cells - includes erythroblasts, plasma cells; excludes megakaryocytes.
      • Peripheral blood: 200 leukocytes.

Required clinical information

  • CBC - usu. macrocytic anemia.
  • Rx - may be Rx effect.
  • Peripheral blood film.
  • Clinical history (symptoms/presentation/PMHx).

Laboratory work-up

  • H&E stain.
  • Giemsa/Wright stain.
  • Iron stain.
  • Gomori silver stain.

DDx of MDS

  1. Nutritional deficiency.
    • Vitamin B12.
    • Folate.
  2. Toxic exposures.
    • Rx.
      • G-CSF.
    • Biologic agents.
    • Heavy metals.
    • Chemotherapy.
  3. Infections.
    • Parovirus B19.
  4. Other.
    • Paroxysmal nocturnal hemoglobinuria (PNH).[2] (???)
    • Congenital hematopoietic disorder.
      • Congenital dyserythropoietic anemia.


Bone marrow specimens

Normal

  • Age (years) ~ percentage of fat.
    • Example 80 years old has ~ 80% fat in marrow space.

Erythroblasts:

  • Typically away from bone.

Megakaryocytes:

  1. Alone - not in clusters.
  2. Not close to bone.

Myeloid cells:

  • Adjacent to bone.

Histologic features

  • Auer rods - used to be diagnostic of MDS regardless of blast count.

Dyserythropoiesis

  • Abnormal RBC formation.

Histology

Nuclear

Features:[1]

  • Nuclear budding.
  • Intranuclear bridging (nuclei fail to separate post-division).
  • Multinucleation.
  • Megablastoid change.
    • May be hard to see.
  • Karyorrhexis (nuclear fragmentation).

Cytoplasmic

Features:[1]

  • Ring sideroblasts.
    • Rim of RBC has ring of iron.
  • Vacuolization.

Dysgranulopoiesis

  • Abnormal granulocyte formation.

Histology

Features:[1]

  • Nuclear hypolobation (pseudo-Pelger-Huet).
  • Hypersegmentation.
    • May be seen in vitamin B12 deficiency, Rx.
  • Cytoplasmic hypogranulation.
  • Pseudo-Chediak-Higashi granules.
  • Small size.

Dysmegakaryocytopoiesis

  • Abnormal megakaryocyte formation.

Histology

Features:[1]

  • Micromegakaryoctes with ypolobated nuclei.
  • Non-lobated nuclei of any size.
  • Multiple widely separated nuclear lobes.

See also

References

  1. 1.0 1.1 1.2 1.3 1.4 1.5 D. Good. 21 March 2011.
  2. URL: http://emedicine.medscape.com/article/207468-overview. Accessed on: 29 May 2011.