Difference between revisions of "Acute myeloid leukemia"

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Abbreviated ''[[AML]]''.
'''Acute myeloid leukemia''', abbreviated '''AML''', is a group of [[cancer|malignancies]].


=No recurrent cytogenetic abnormalities=
==Acute myeloid leukemia without recurrent cytogenetic abnormalities==
===General===
===General===
*Adults.
*Adults.
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*May be classified by morphology, using the (old) French-American-British (FAB) classification (M0-M7).
*May be classified by morphology, using the (old) French-American-British (FAB) classification (M0-M7).


====Image====
===Image===
<gallery>
<gallery>
Image:Auer_rods.PNG | Auer rods in an AML. (WC)
Image:Auer_rods.PNG | Auer rods in an AML. (WC)
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*Must exclude all the recurrent cytogenetic abnormalities - see below.
*Must exclude all the recurrent cytogenetic abnormalities - see below.


==AML with recurrent cytogenetic abnormalities==
=AML with recurrent cytogenetic abnormalities=
===Acute myeloid leukemia with t(8;21)===
==Acute myeloid leukemia with t(8;21)==
*t(8;21)(q22;q22).<ref>{{Cite journal  | last1 = Berger | first1 = R. | title = Translocation t(8;21)(q22;q22): cytogenetics and molecular biology. | journal = Nouv Rev Fr Hematol | volume = 36 Suppl 1 | issue =  | pages = S67-9 | month =  | year = 1994 | doi =  | PMID = 8177719 }}</ref>
*t(8;21)(q22;q22).<ref>{{Cite journal  | last1 = Berger | first1 = R. | title = Translocation t(8;21)(q22;q22): cytogenetics and molecular biology. | journal = Nouv Rev Fr Hematol | volume = 36 Suppl 1 | issue =  | pages = S67-9 | month =  | year = 1994 | doi =  | PMID = 8177719 }}</ref>


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*[http://path.upmc.edu/cases/case712.html AML with t(8;21) (upmc.edu)].
*[http://path.upmc.edu/cases/case712.html AML with t(8;21) (upmc.edu)].


===Acute myeloid leukemia with inv(16)===
==Acute myeloid leukemia with inv(16)==
*inv(16)(p13.1q22).<ref name=pmid16917916>{{Cite journal  | last1 = Lu | first1 = CM. | last2 = Murata-Collins | first2 = JL. | last3 = Wang | first3 = E. | last4 = Siddiqi | first4 = I. | last5 = Lawrence | first5 = HJ. | title = Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases. | journal = Am J Hematol | volume = 81 | issue = 12 | pages = 963-8 | month = Dec | year = 2006 | doi = 10.1002/ajh.20716 | PMID = 16917916 }}
*inv(16)(p13.1q22).<ref name=pmid16917916>{{Cite journal  | last1 = Lu | first1 = CM. | last2 = Murata-Collins | first2 = JL. | last3 = Wang | first3 = E. | last4 = Siddiqi | first4 = I. | last5 = Lawrence | first5 = HJ. | title = Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases. | journal = Am J Hematol | volume = 81 | issue = 12 | pages = 963-8 | month = Dec | year = 2006 | doi = 10.1002/ajh.20716 | PMID = 16917916 }}
</ref>
</ref>
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*CD2+ -- common.
*CD2+ -- common.


===Acute myeloid leukemia with t(15;17)===
==Acute myeloid leukemia with t(15;17)==
*[[AKA]] ''acute promyelocytic leukemia''
*[[AKA]] ''acute promyelocytic leukemia''
**Abbreviated ''APL''.
**Abbreviated ''APL''.
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**Fusion transcripts: PML<ref name=omim102578>{{OMIM|102578}}</ref>-RARA.<ref name=omim180240>{{OMIM|180240}}</ref>
**Fusion transcripts: PML<ref name=omim102578>{{OMIM|102578}}</ref>-RARA.<ref name=omim180240>{{OMIM|180240}}</ref>


====General====
==General==
Clinical:
Clinical:
*Associated with [[DIC]].
*Associated with [[DIC]].
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*t(5;17). (???)
*t(5;17). (???)


====Microscopic====
==Microscopic==
Comes in two flavours.
Comes in two flavours.


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*Absence of granules on light microscopy.
*Absence of granules on light microscopy.


=====Images=====
===Images===
<gallery>
<gallery>
Image:Faggot cell in AML-M3.jpg |Faggot cell in AML-M3. (WC)
Image:Faggot cell in AML-M3.jpg |Faggot cell in AML-M3. (WC)
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*[http://path.upmc.edu/cases/case705.html APML - several images (upmc.edu)].
*[http://path.upmc.edu/cases/case705.html APML - several images (upmc.edu)].


====IHC====
===IHC===
*CD2 +ve, CD34 +ve/-ve, CD56 +ve/-ve.
*CD2 +ve, CD34 +ve/-ve, CD56 +ve/-ve.


====[[Flow cytometry]]====
===[[Flow cytometry]]===
*CD34 -ve, HLA-DR -ve.
*CD34 -ve, HLA-DR -ve.
*CD33 +ve, CD13 +ve/-ve, CD117 +ve (weak), CD56 +ve/-ve.
*CD33 +ve, CD13 +ve/-ve, CD117 +ve (weak), CD56 +ve/-ve.


===Acute myeloid leukemia with t(9;11)===
==Acute myeloid leukemia with t(9;11)==
*t(9;11).
*t(9;11).


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*CD34+. (???)
*CD34+. (???)
*CD13+. (???)
*CD13+. (???)
=See also=
*[[Leukemia]].
=References=
{{Reflist|1}}


[[Category: Hematopathology]]
[[Category: Hematopathology]]

Revision as of 23:28, 27 May 2018

Acute myeloid leukemia, abbreviated AML, is a group of malignancies.

No recurrent cytogenetic abnormalities

Acute myeloid leukemia without recurrent cytogenetic abnormalities

General

  • Adults.

Exclusions for this diagnosis:

Microscopic

Features:

  • Auer rods present
  • Cytoplasmic granularity.
  • Large cells.

Note:

  • May be classified by morphology, using the (old) French-American-British (FAB) classification (M0-M7).

Image

www:

Molecular

  • Must exclude all the recurrent cytogenetic abnormalities - see below.

AML with recurrent cytogenetic abnormalities

Acute myeloid leukemia with t(8;21)

  • t(8;21)(q22;q22).[1]

IHC:

  • CD34+, CD13+, MPO+ (cytoplasm), CD33+ (weak).
  • CD56+, CD117+.
    • Usu. assoc. with a bad prognosis.

Flow cytometry:

  • CD19+, PAX5+, CD79a +/-.

Images:

Acute myeloid leukemia with inv(16)

  • inv(16)(p13.1q22).[2]

Microscopic:

  • Blast count usu. ~20% (low).
  • Eosinophilic granules.
    • Used to be classified as "M4" with eosinophilia.

IHC:

  • CD2+ -- common.

Acute myeloid leukemia with t(15;17)

  • AKA acute promyelocytic leukemia
    • Abbreviated APL.
  • t(15;17)(q22;q12).
    • Fusion transcripts: PML[3]-RARA.[4]

General

Clinical:

  • Associated with DIC.
  • Treatment: all-trans retinoic acid (ATRA).

Variants:

  • t(11;17) -- ATRA doesn't work.[5]
  • t(17;17) -- ATRA doesn't work.
  • t(5;17). (???)

Microscopic

Comes in two flavours.

Microscopic (Hypergranular or typical APL):

  • Bean-shaped nucleus or bilobed nucleus.
  • Buddles of Auer rods - known as "Faggot cells".

Microscopic (Microgranular or hypogranular APL):

  • Bilobed nuclei with nuclear overlap. (???)
  • Absence of granules on light microscopy.

Images

www:

IHC

  • CD2 +ve, CD34 +ve/-ve, CD56 +ve/-ve.

Flow cytometry

  • CD34 -ve, HLA-DR -ve.
  • CD33 +ve, CD13 +ve/-ve, CD117 +ve (weak), CD56 +ve/-ve.

Acute myeloid leukemia with t(9;11)

  • t(9;11).

Microscopic:

  • Monoblastic morphology. (???)
  • Myelomonocytic morphology. (???)

Clinical:

  • +/-DIC.
  • Usu. children.

IHC:

  • CD33+, CD65+, CD4+, HLA-DR+.
  • CD34+. (???)
  • CD13+. (???)

See also

References

  1. Berger, R. (1994). "Translocation t(8;21)(q22;q22): cytogenetics and molecular biology.". Nouv Rev Fr Hematol 36 Suppl 1: S67-9. PMID 8177719.
  2. Lu, CM.; Murata-Collins, JL.; Wang, E.; Siddiqi, I.; Lawrence, HJ. (Dec 2006). "Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases.". Am J Hematol 81 (12): 963-8. doi:10.1002/ajh.20716. PMID 16917916.
  3. Online 'Mendelian Inheritance in Man' (OMIM) 102578
  4. Online 'Mendelian Inheritance in Man' (OMIM) 180240
  5. Lefkowitch, Jay H. (2006). Anatomic Pathology Board Review (1st ed.). Saunders. pp. 623 Q2. ISBN 978-1416025887.
  6. URL: http://path.upmc.edu/cases/case457.html. Accessed on: 21 January 2012.