Undifferentiated blasts, AML- -not otherwise categorized
M0 myeloid
Blasts and promyelocytes predominate without further maturation of myeloid cells
M1 myeloid
Myeloid cells demonstrate maturation beyond the blast and promyelocyte stage
M2 myeloid
Promvelocytes predominate in the bone marrow
Promvelocytes predominate in the bone marrow
M3 promyelocytic
Both myeloid and monocytic cells are present to the extent of at least 20% of the total leukocytes
M4 myelomonocytic
Most cells are monocytic; two subtypes (a and b) are recognized, one characterized by large blasts in bone marrow and peripheral blood, the other (differentiated type) by monoblasts, promonocytes, and monocytes
M5 monocytic
Also known as Di Guglielmo syndrome; abnormal proliferation of both erythroid and granulocytic precursors; may include abnormal megakaryocytic and monocytic proliferations
M6 erythroleukemia
Large and small megakaryoblasts with a high nuclear-cytoplasmic ratio; pale, agranular cytoplasm
M7 megakaryocytic
is characterized by either a rapid or gradual onset that may resemble an acute infection. The patient may have a history of fever, infections, fatigue, and bleeding episodes. Physical examination may reveal tenderness of the bones, particularly the ribs and sternum; ulcerated mucous membranes; petechiae; and purpura. Additional physical findings may include hepatomegaly, splenomegaly, and lymphadenopathy.
FAB M1
The outstanding feature of the peripheral blood smear and bone marrow is the predominance of myeloblasts. These blasts usually have a regular cytoplasmic outline and may contain slender, red- staining Auer rods in the cytoplasm. The nuclear chromatin is very fine and homogeneous
M1
Associated with CHLOROMA = localized tumor masses consisting of myeloblasts. In these tumors, the presence of large quantities of the enzyme MPO produces a green appearance if the tissue is cut
M1
Hemorrhagic manifestations such as easy bruising, epistaxis, gingival bleeding, and petechiae are common initial symptoms. Hepatomegaly, splenomegaly, and lymphadenopathy are seen infrequentl
M2
Myeloblasts predominate on peripheral blood smears. The nuclei are usually round or oval with one or more prominent nucleoli and fi ne reticular chromatin. The cytoplasm is basophilic with a variable number of azurophilic granules. Auer rods are commonly seen
M2
Fatigue and symptoms of bleeding such as bruising, hematuria, and petechiae are common. Hepatomegaly, splenomegaly, and lymphadenopathy are seen infrequently.
M3
Appears to be the most aggressive of acute leukemia with a severe bleeding tendency and a fatal course
Promyelocytes are the predominating cell type
M3
The promyelocytes may be hypergranular, microgranular, or hypogranular variations. Coarsely granular
promyelocytes with dumbbell-shaped or bilobed nuclei may be seen. The nuclear chromatin is finely reticular and
the cells often lack nucleoli
M3
is characterized by a balanced reciprocal translocation between chromosomes 15 and 17, which results in
the fusion between PML gene and retinoic acid receptor a (RARA)
It is associated with DIC
M3
This form of leukemia may also be referred to as Naegeli type monocytic leukemia. Occurrence of this form of leukemia is uncommon in children and young adults. The highest frequency of occurrence is in adults older than 50 years of age
M4
Symptoms of this form of leukemia are similar to those of other forms of acute leukemia. Pharyngitis may be observed. Gingival hyperplasia due to leukemic infiltration may be noted
Associated with leukostasis together with M5
M4
Leukostasis refers to a pathological finding of slightly dilated, thin-walled vessels filled with leukemic cells. The brain
and lungs are the most commonly involved organs. Symptoms of leukostasis are headache, visual impairment, and
shortness of breath
proliferation of granulocytes and monocytes is characteristic.
M4