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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_2768_Библиотеки_им_академика_М_И_Перельмана
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CHAPTER 15 Acute Myeloid Leukemia
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MORPHOLOGY:
Peripheral Blood: Blasts with some maturation ± Auer rods (see Figures 15.2)
Bone Marrow: Blasts, some with large azurophilic granules, perinuclear hof± Auer rods
Less than 90% of nonerythroid cells are blasts
10% or higher neutrophilic component
Less than 20% monocytic component
CYTOCHEMISTRY:
Myeloperoxidase: Positive (see Figure 15.2E)
Sudan Black B: Positive (see Figure 15.2F)
GENETICS:
Subset with t(8;21) is designated as AML with recurrent genetic abnormalities. In this subset, blasts are large
with abundant basophilic cytoplasm, azurophilic granules, and possible perinuclear hofs.
IMMUNOPHENOTYPE:
+
+
CD13
, CD33
, CD65
+
, CD11b
+
, CD15
+
, HLA-DR
±
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SECTION 4 Leukocytes
B
ACUTE PROMYELOCYTIC LEUKEMIA WITH PML-RARA FAB M3
B
A
A
FIGURE 15.4A Peripheral blood. A, Hypergranular
promyelocyte (×1000); B, Faggot cells.
C
FIGURE 15.4C Bone marrow ( ×1000).
B
FIGURE 15.4B Bone marrow ( ×500).
MORPHOLOGY:
Peripheral Blood: White blood cell count may be low
or only slightly elevated
Hypergranular abnormal promyelocytes, pink to purple
cytoplasm; nucleus may be folded or bilobed
Multiple Auer rods possible, may be in bundles,
schistocytes
Bone Marrow: Hypergranular abnormal
promyelocytes, pink to purple cytoplasm; nucleus
may be folded or bilobed
± Multiple Auer rods
CYTOCHEMISTRY:
Myeloperoxidase: Strongly positive (see Figure 15.2E)
Sudan Black B: Strongly positive (see Figure 15.2F)
GENETICS:
t(15;17) is sufcient for diagnosis as AML with recurrent
genetic abnormalities regardless of blast/promyelocyte
‡
count.
IMMUNOPHENOTYPE:
±
CD13
+
, CD33
, CD34 , HLA-DR , CD15 , CD65 , CD117
+
‡
Abnormal promyelocytes are considered blast equivalents for the purpose of diagnosis.
NOTE: Acute promyelocytic leukemia may be associated
with disseminated intravascular coagulopathy.

CHAPTER 15 Acute Myeloid Leukemia
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ACUTE PROMYELOCYTIC LEUKEMIA WITH PML-RARA: MICROGRANULAR VARIANT
(HYPOGRANULAR) VARIANT FAB M3
149
A
FIGURE 15.5A Peripheral blood ( ×1000).
MORPHOLOGY:
Peripheral Blood: White blood cell count markedly
elevated; deeply notched nuclei
Cytoplasm may appear agranular because of submicro-
scopic size of granules, which are evident with electron microscopy
Bone Marrow: Agranular promyelocytes, with deeply
notched nuclei
CYTOCHEMISTRY:
Myeloperoxidase: Strongly positive (see Figure 15.2E)
Sudan Black B: Strongly positive (see Figure 15.2F)
GENETICS:
t(15;17) is sufcient for diagnosis as AML with recurrent
genetic abnormalities regardless of blast/promyelocyte
count.
IMMUNOPHENOTYPE:
CD13
CD15
±
−
, CD33
, CD65
+
, CD34
−
−
, HLA-DR
−
, CD64
+
, CD117
B
FIGURE 15.5B Bone marrow ( ×500).
C
±
,
FIGURE 15.5C Bone marrow ( ×1000).
NOTE: Microgranular promyelocytes can be confused
morphologically with monocyte precursors.

150
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SECTION 4 Leukocytes
ACUTE MYELOMONOCYTIC LEUKEMIA
FAB M4
A
FIGURE 15.6A Peripheral blood ( ×1000).
NOTE: Promonocyte at arrow
B
FIGURE 15.6B Bone marrow ( ×500).
C
FIGURE 15.6C Bone marrow ( ×1000).
NOTE: Pseudopod at arrow
D
FIGURE 15.6D Positive naphthol-AS-D chloroacetate
esterase (specic) stain.

CHAPTER 15 Acute Myeloid Leukemia
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151
E
FIGURE 15.6E Positive myeloperoxidase (500 ×).
(Courtesy George Girgis, CLS, IU Health).
F
FIGURE 15.6F Positive α-Naphthyl butyrate esterase
(×1000). (Courtesy George Girgis, CLS, IU Health).
MORPHOLOGY:
Peripheral Blood: Myeloblasts, promyelocytes, and other immature myeloid precursors
Monoblasts, promonocytes, and monocytes; frequently more mature than those seen in bone marrow
± Auer rods (see Figure 15.2B)
Bone Marrow: Monoblasts have round nuclei with abundant moderate to intensely basophilic cytoplasm
Possible pseudopod formations, vacuoles, and Auer rods are possible
Nuclear chromatin is ne with one or more prominent nucleoli
Promonocytes are delicately convoluted nucleus with ne chromatin and prominent nucleoli; cytoplasm is not
as basophilic as the monoblast and may be more obviously granulated with occasional large azurophilic
granules and vacuoles
Eosinophils are increased and abnormal with many large, immature granules
CYTOCHEMISTRY:
Myeloperoxidase: Blast ≥ 3% positive (see Figure 15.2E)
Specic Esterase: Naphthol-AS-D chloroacetate esterase is positive in granulocytic cells and weak in mono-
cytic cells (see Figure 15.6D)
Nonspecic Esterase:
• α-Naphthyl acetate esterase: weakly positive or absent in monocytic cells. (Figure15.6E); inhibited by NaFl
(Figure15.6F)
• α-Naphthyl butyrate esterase: positive or absent in monocytic cells (see Figure 15.8D)
GENETICS:
Recurrent genetic abnormalities: not dened.
NOTE: inv(16) or t(16;16) and abnormal eosinophils are excluded from this category.
IMMUNOPHENOTYPE:
+
CD13
, CD33
+
, CD14
+
, CD4
+
, CD11b
+
, CD64
+
, CD15
+
, CD36
+

152
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SECTION 4 Leukocytes
ACUTE MYELOID LEUKEMIA WITH inv(16) (13.1;q22) OR
t(16;16) (p13.1;q22); CBFB-MYH11
Acute Myeloid Leukemia With Abnormal Marrow Eosinophils
FAB M4EO
A
FIGURE 15.7A Peripheral blood ( ×1000).
B
FIGURE 15.7B Bone marrow ( ×500).
C
FIGURE 15.7C Bone marrow ( ×1000).
D
FIGURE 15.7D Bone Marrow ( ×500). Eosinophil with
immature granules (arrow)
(Courtesy George Girgis, (CLS) IU Health).

CHAPTER 15 Acute Myeloid Leukemia
https://t.me/medicina_free
MORPHOLOGY:
Peripheral Blood: Myeloblasts, monoblasts, promyelocytes, and other immature myeloid precursors
Monoblasts, promonocytes, and monocytes
Bone marrow ± Auer rods (see Figure 15.2B)
Bone Marrow: Monoblasts have round nuclei with abundant moderate to intensely basophilic cytoplasm
Possible pseudopod formations, vacuoles, and Auer rods are possible
Nuclear chromatin is ne with one or more prominent nucleoli
Promonodytes have delicately convoluted nucleus with ne chromatic and prominent nucleoli; cytoplasm is
not as basophilic as the monoblast and may be more obviously granulated with occasional large azurophilic
granules and vacuoles
Eosinophils are increased and abnormal with many large, immature granules
CYTOCHEMISTRY:
Myeloperoxidase: Blast ≥3% positive (see Figure 15.2E)
Nonspecic Esterase: Positive
Specic Esterase: Weakly positive in abnormal eosinophils
GENETICS:
Recurrent genetic abnormality: inv(16).
IMMUNOPHENOTYPE:
+
+
+
CD13
, CD33
, CD14
, CD4
+
, CD11b
+
, CD11c
+
, CD64
+
, CD15
+
, CD36
+
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SECTION 4 Leukocytes
ACUTE MONOBLASTIC AND MONOCYTIC LEUKEMIA
FAB M5
A
FIGURE 15.8A Peripheral blood: monoblasts
predominate ( ×1000).
C
FIGURE 15.8C Bone marrow showing monoblast
predominance ( ×500).
B
FIGURE 15.8B Peripheral blood: promonocytes
predominate ( ×1000).
D
FIGURE 15.8D Positive α-naphthyl butyrate esterase
(nonspecic) esterase stain.

CHAPTER 15 Acute Myeloid Leukemia
https://t.me/medicina_free
MORPHOLOGY:
Peripheral Blood: Monoblasts, promonocytes, monocytes
Bone Marrow: ≤ Bone marrow cells are of granulocytic lineage
Monoblasts have round nuclei with abundant moderate to intensely basophilic cytoplasm
Possible pseudopod formations, vacuoles, and Auer rods are possible
Nuclear chromatin is ne with one or more prominent nucleoli.
Promonocytes have delicately convoluted nucleus with ne chromatin and prominent nucleoli; cytoplasm is
not as basophilic as the monoblast and may be more obviously granulated with occasional large azurophilic
granules and vacuoles
≥ 80% have monocytic morphology; ≤20% granulocyte morphology
Hint: In monoblastic leukemia, the majority of bone marrow cells are monoblasts.
In monocytic leukemia, the majority of bone marrow cells are promyelocytes.
CYTOCHEMISTRY:
Myeloperoxidase: Negative (may have some weak activity in promonocytes)
Nonspecic Esterase: Positive
GENETICS:
Recurrent genetic abnormality: t(9;11), common in children.
IMMUNOPHENOTYPE:
+
CD14
, CD4
+
, CD11b
+
, CD64
+
, CD68
+
, HLA-DR
+
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SECTION 4 Leukocytes
ACUTE ERYTHROID LEUKEMIA
FAB M6a
(Pure Erythroid Leukemia)
A
FIGURE 15.9A Peripheral blood ( ×1000).
C
FIGURE 15.9C Bone marrow: pure erythroid
leukemia (×500).
B
FIGURE 15.9B Bone marrow: erythroid/myeloid
leukemia (×500).
D
FIGURE 15.9D Positive periodic acid–Schiff stain.
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