Normal Lab Values
Hematopoietic System
Readings from Robbins Basic Pathol, 9th ed.
by TUESDAY
by THURSDAY
 
 
pages
topics
pages
topics
 
Lab Sections 1, 2, and 3
pp 407 - 425
Ch 11 intro - Polycythemia

pp 425 - 449

White cell disorders - Histiocytic neoplasms
 
 
pp 449 - 455
Bleeding disorders - Hemophilia B
     
           
Lab Sections 4 and 5

pp 425 - 449

White cell disorders - Histiocytic neoplasms
pp 407 - 425
Ch 11 intro - Polycythemia
 
     
pp 449 - 445
Bleeding disorders - Hemophilia B
 
 

Case assignments by lab group and class day:

  TUESDAY THURSDAY
Labs 1, 2, & 3
Labs 4 & 5

 

CASE NUMBER 508 - slide courtesy of the University of British Columbia
[ImageScope] [WebScope]

Clinical History: A 65-year-old African-American man presented to his primary care physician with a 6-month history of fatigue and weakness and a 2-month history of a burning/tingling sensation in both feet.  Physical exam revealed pale mucous membranes and a reddened, smooth tongue. Laboratory analysis showed an increased MCV, a decreased hematocrit and serum antibodies to intrinsic factor. A peripheral smear and a subsequent gastric biopsy are provided for evaluation.

Image Gallery:

(Summary of Microscopic Findings)

The prominent microscopic finding in this peripheral blood smear is the presence of a neutrophil with a nucleus showing at least seven segments. This is called hypersegmentation. The cytoplasm contains appropriate granules. The red blood cells show mild variation in size (anisocytosis). Some large, oval red blood cells are present, and these oval macrocytes show reduced central pallor. Central pallor is not increased in red cells overall. Platelets appear to have normal morphology.

The gastric biopsy shows loss of parietal cells and intestinal metaplasia. There is a deeply seated mixed inflammatory infiltrate consisting of lymphocytes, macrophages and plasma cells.

(Review Blood Histology)
Norm No. 29 Lymph node

Normal blood smear 63x (Wright stain)
[ImageScope] [WebScope]

Normal blood smear 86x (Wright stain)
[ImageScope] [WebScope]

Scan around the 63x and 86x slides at high magnification to see the various kinds of blood cells that were discussed in the lecture.  Most abundant, of course, are the red blood cells (RBCs) or erythrocytes, which are seen in large numbers everywhere you look.  In between the RBCs you should look for small, basophilic fragments which are platelets or thrombocytes [example] that are important in blood clotting.  As you continue viewing, you will see occasional white blood cells (leukocytes).  Some of the white blood cells may defy identification, often because the cells were damaged during slide preparation, so look for characteristic examples, and ignore the equivocal cells. Refer to the images in your texts and from the lecture and try to find an example of each leukocyte type using the 63x and 86x slides (there's less area to cover in these high-mag slides and the cells present are excellent, although the 63x slide does NOT contain any basophils).

The most common white blood cell is the neutrophil, which has a distinct multi-lobed nucleus (often 3-5 lobes).  Also frequently seen are lymphocytes, which are small cells (often as small as RBCs) with a dark nucleus and very little cytoplasm.  Another cell type is the monocyte, the largest of the blood cells.  It has a large, relatively pale nucleus, and rather clear cytoplasm (granules are usually less apparent than those in the illustration in W).  You will also see an occasional eosinophil, with prominent reddish granules filling the cytoplasm, and a nucleus with 2 (or sometimes 3) lobes.  The exact color of the granules may vary from slide to slide, depending on how well the slide was prepared.  In your particular slides they may be anywhere from bright red to dull brown.  The remaining cell type you may see on your slides is the basophil, which is hard to find, since it constitutes less than 1% of the leukocytes (the 86x slide actually has THREE excellent examples).  The cytoplasm contains large, irregular granules in a "grape-cluster" appearance that usually stain dark blue or almost black. Basophil nuclei may often appear somewhat oval-shaped, so, at first glance, they may be confused with lymphocytes. However, the presence of the large, dark-staining granules should help you distinguish them; also, remember that basophils are rare.

After you've done some looking on your own, here some quick links showing examples of each type of leukocyte (in order of their normal frequency in a blood smear):

508-1. What is the differential diagnosis?

ANSWER

 

508-2. Which of the following is the most appropriate treatment?

  1. Bone marrow transplant
  2. High dose vitamin B12
  3. Iron supplementation
  4. Monthly blood transfusions
  5. Splenectomy

ANSWER

 

508-3. Which of the following is the most common cause of this condition?

  1. Chronic renal failure
  2. Infection with parvovirus B19
  3. Iron deficiency
  4. Pernicious anemia
  5. Trauma to red blood cells

ANSWER

 

508-4. This patient has an increased risk of developing which of the following?

  1. Aortic aneurysm
  2. Cirrhosis of the liver
  3. Diffuse large B-cell lymphoma
  4. Gastric carcinoma
  5. Splenic infarction

ANSWER

 

CASE NUMBER 513
(no virtual slides for this case)

Clinical History: A 29-year-old woman who was diagnosed with celiac disease 6 months earlier presents to her primary care physician with a 3-week history of fatigue and dizziness. She states that she has not followed her doctor’s dietary recommendations. Physical exam was significant for noticeable pallor. Laboratory analysis showed a hemoglobin of 7 gm/dL, serum ferritin of 10 nanograms/mL (normal range female 12-150 ng/mL) and an RDW of 20% (normal 11.5-14.5%) .  A peripheral smear is shown below.

Image Gallery:

(Summary of Microscopic Findings)

The red cells show moderate variation in size and shape (aniso-poikilocytosis), including some teardrop cells and oval cells. The central pallor in most red cells is increased (> a third of cell diameter) indicating hypochromia. A lymphocyte is present without significant abnormality. Only four platelets are present in this picture and platelet count may be low, but they show variation in size and the presence of a large platelet indicates active production. (Note: Platelet count is often high in iron deficiency).

(Review Blood Histology)
Norm No. 29 Lymph node

Normal blood smear 63x (Wright stain)
[ImageScope] [WebScope]

Normal blood smear 86x (Wright stain)
[ImageScope] [WebScope]

Scan around the 63x and 86x slides at high magnification to see the various kinds of blood cells that were discussed in the lecture.  Most abundant, of course, are the red blood cells (RBCs) or erythrocytes, which are seen in large numbers everywhere you look.  In between the RBCs you should look for small, basophilic fragments which are platelets or thrombocytes [example] that are important in blood clotting.  As you continue viewing, you will see occasional white blood cells (leukocytes).  Some of the white blood cells may defy identification, often because the cells were damaged during slide preparation, so look for characteristic examples, and ignore the equivocal cells. Refer to the images in your texts and from the lecture and try to find an example of each leukocyte type using the 63x and 86x slides (there's less area to cover in these high-mag slides and the cells present are excellent, although the 63x slide does NOT contain any basophils).

The most common white blood cell is the neutrophil, which has a distinct multi-lobed nucleus (often 3-5 lobes).  Also frequently seen are lymphocytes, which are small cells (often as small as RBCs) with a dark nucleus and very little cytoplasm.  Another cell type is the monocyte, the largest of the blood cells.  It has a large, relatively pale nucleus, and rather clear cytoplasm (granules are usually less apparent than those in the illustration in W).  You will also see an occasional eosinophil, with prominent reddish granules filling the cytoplasm, and a nucleus with 2 (or sometimes 3) lobes.  The exact color of the granules may vary from slide to slide, depending on how well the slide was prepared.  In your particular slides they may be anywhere from bright red to dull brown.  The remaining cell type you may see on your slides is the basophil, which is hard to find, since it constitutes less than 1% of the leukocytes (the 86x slide actually has THREE excellent examples).  The cytoplasm contains large, irregular granules in a "grape-cluster" appearance that usually stain dark blue or almost black. Basophil nuclei may often appear somewhat oval-shaped, so, at first glance, they may be confused with lymphocytes. However, the presence of the large, dark-staining granules should help you distinguish them; also, remember that basophils are rare.

After you've done some looking on your own, here some quick links showing examples of each type of leukocyte (in order of their normal frequency in a blood smear):

513-1. What is the differential diagnosis?

ANSWER

 

513-2. This patient’s decreased iron levels are most likely due to which of the following?

  1. Decreased hepcidin production
  2. Decreased transferrin levels
  3. Dihydrofolate reductase inhibition
  4. Impaired iron absorption
  5. Occult bleeding due to peptic ulcer disease

ANSWER

 

513-3. Which of the following is the most common cause of this type of anemia in the Western world?

  1. Chloramphenicol treatment
  2. Chronic blood loss
  3. Rheumatoid arthritis
  4. Inherited defects of telomerase
  5. Vegetarian diet

ANSWER

 

 

CASE NUMBER 413
[ImageScope] [WebScope]

Clinical History: A 57-year-old man presented to his primary care physician with a 3-month history of back pain and 2-week history of fatigue and weakness. Plain radiograph showed lytic lesions in multiple bones and urinalysis revealed Bence Jones protein. Laboratory analysis showed anemia. A bone marrow biopsy was performed and, based on the diagnosis, chemotherapy and radiation were initiated; however, the patient developed sepsis and died. Radiography, gross and microscopic images are provided.

Image Gallery:

(Summary of Gross and Radiographic Findings)
Many of the bones contained poorly delineated, soft gelatinous red tumor masses of various dimensions. Plain film of the skull shows sharply punched out bone lesions.
(Summary of Microscopic Findings)
The marrow is heavily infiltrated with plasma cells which vary in degree of maturation. Islets of normoblasts are present, but granulocytes and megakaryocytes are markedly decreased. There is considerable loss of trabecular and cortical bone.
(Review Bone Marrow Histology)
Specimen No. 67. Bone marrow, human, H&E
[ImageScope] [WebScope]

A thin layer of compact/dense bone borders this section, with internal cancellous/spongy bone. The spaces between bony spicules are filled with hematopoietic cells. Not the large numbers of (round, empty) fat cells present within the marrow space. The fat is lost during processing into paraffin sections. Megakaryocytes can be readily identified, since they are approximately 5-fold larger than most bone marrow cells and contain strongly eosinophilic cytoplasm and multiple nuclei.

(slide and description courtesy of Dr. Laura Hale, Duke PATHOL725 course director)

413-1. What is the differential diagnosis?

ANSWER

 

413-2. Which of the following additional findings is most likely in this patient?

  1. Abundant pulmonary histiocytes
  2. Amyloidosis
  3. Multiple cutaneous lesions
  4. Polycythemia
  5. Thrombocytosis

ANSWER

 

413-3. Which of the following is true regarding this disease?

  1. IgM is the most common serum Ig
  2. Most patients live >10 years after diagnosis
  3. Renal insufficiency is rarely the cause of death
  4. Soft tissue involvement can be seen in advanced disease
  5. Transformation to diffuse large B cell lymphoma is seen in 25% of patients

ANSWER

 

413-4. Which of the following chromosomal alterations is associated with this disease?

  1. ALK rearrangements
  2. del 13q14.3
  3. Hyperdiploidy
  4. t(11;14)
  5. t(14;18)

ANSWER

 

 

CASE NUMBER 295, UMich slide 40092nl
[ImageScope] [WebScope] -courtesy of UMich

Clinical History: A 16-year-old boy presented to his pediatrician with a 3 cm mass on right side of his neck. This mass was biopsied. Following diagnosis, a screening CT was performed and revealed a mediastinal mass. Gross and microscopic images of the neck mass biopsy are provided.

Image Gallery:

(Summary of Gross Findings)
The lymph node was enlarged, and remarkable for fibrous bands separating areas of firm, fleshy material.
(Summary of Microscopic Findings)
The normal lymph node architecture is completely destroyed. In its place are thick bands of collagen, separating islands of lymphoid tissue. In some of these nodules, there is a mixed infiltrate consisting of lymphocytes, eosinophils, some neutrophils and plasma cells, and numerous large cells with highly pleomorphic nuclei. Nuclei are frequently multi lobulated but classic binucleate Reed-Stemberg cells are uncommon. Many cells are so-called "lacunar variants", with nuclei which have artifactually shrunken away from their cytoplasmic borders, leaving a clear space than can often easily be appreciated at low power.
(Review Lymph Node Histology)
Norm No. 29 Lymph node
[ImageScope] [WebScope]

The lymph node contains a cortex which includes the lymphoid follicles and a medulla which is looser tissue containing the lymphatic channels and blood vessels.

295-1. What is the differential diagnosis?

ANSWER

 

295-2. Which of the following is the proposed line of differentiation of the neoplastic cells?

  1. Germinal center B cells
  2. Marginal zone B cells
  3. Mature T cells
  4. Naïve B cells 
  5. Plasma cells

ANSWER

 

295-2. Which of the following distinguishes this disease from non-Hogdkin lymphomas?

  1. Extranodal involvement is common
  2. Frequently involves peripheral lymph nodes
  3. Mesenteric nodes and Waldeyer ring commonly involved
  4. Orderly spread to contiguous lymph nodes

ANSWER

 

295-4.Which of the following is true regarding this disease?

  1. Epstein-Barr virus infection is common
  2. It is the least common subtype in this family of diseases
  3. Lacunar cells are diagnostic
  4. Males are more commonly affected than females
  5. Most patients present with Stage III disease or higher

ANSWER

 

 

CASE NUMBER 606, UMich slide 02S
[ImageScope] [WebScope] -courtesy of UMich

Clinical History: A 3-year old boy presents with epistaxis and fever. Multiple cutaneous petechiae are evident, and there is generalized enlargement of lymph nodes, as well as palpable splenomegaly. The hemoglobin and platelet count are markedly decreased, and the white blood cell count is elevated to 40,000 cells/uL, with a preponderance of lymphoblasts. The peripheral blood film is shown.

Image Gallery:

(Summary of Microscopic Findings)

Red cells show mild anisocytosis with slight hypochromia. The white cells are all blasts, about 2.5x the diameter of red cells which contain round, oval or slightly indented nuclei containing a fine uniform chromatin and 0-1 small nucleoli. There is a small amount of pale blue, agranular cytoplasm. Platelets are not seen.

(Review Blood Histology)
Norm No. 29 Lymph node

Normal blood smear 63x (Wright stain)
[ImageScope] [WebScope]

Normal blood smear 86x (Wright stain)
[ImageScope] [WebScope]

Scan around the 63x and 86x slides at high magnification to see the various kinds of blood cells that were discussed in the lecture.  Most abundant, of course, are the red blood cells (RBCs) or erythrocytes, which are seen in large numbers everywhere you look.  In between the RBCs you should look for small, basophilic fragments which are platelets or thrombocytes [example] that are important in blood clotting.  As you continue viewing, you will see occasional white blood cells (leukocytes).  Some of the white blood cells may defy identification, often because the cells were damaged during slide preparation, so look for characteristic examples, and ignore the equivocal cells. Refer to the images in your texts and from the lecture and try to find an example of each leukocyte type using the 63x and 86x slides (there's less area to cover in these high-mag slides and the cells present are excellent, although the 63x slide does NOT contain any basophils).

The most common white blood cell is the neutrophil, which has a distinct multi-lobed nucleus (often 3-5 lobes).  Also frequently seen are lymphocytes, which are small cells (often as small as RBCs) with a dark nucleus and very little cytoplasm.  Another cell type is the monocyte, the largest of the blood cells.  It has a large, relatively pale nucleus, and rather clear cytoplasm (granules are usually less apparent than those in the illustration in W).  You will also see an occasional eosinophil, with prominent reddish granules filling the cytoplasm, and a nucleus with 2 (or sometimes 3) lobes.  The exact color of the granules may vary from slide to slide, depending on how well the slide was prepared.  In your particular slides they may be anywhere from bright red to dull brown.  The remaining cell type you may see on your slides is the basophil, which is hard to find, since it constitutes less than 1% of the leukocytes (the 86x slide actually has THREE excellent examples).  The cytoplasm contains large, irregular granules in a "grape-cluster" appearance that usually stain dark blue or almost black. Basophil nuclei may often appear somewhat oval-shaped, so, at first glance, they may be confused with lymphocytes. However, the presence of the large, dark-staining granules should help you distinguish them; also, remember that basophils are rare.

After you've done some looking on your own, here some quick links showing examples of each type of leukocyte (in order of their normal frequency in a blood smear):

606-1. What is the differential diagnosis?

ANSWER

 

606-2. Which of the following statements best characterizes this disorder?

  1. It is the form of acute leukemia that is most responsive to therapy
  2. It occurs most often in adults but can occur in children
  3. Lymphoblastic cells cause damage to normal blood cells, resulting in low cell counts
  4. The presence of the CD10 marker is indicative of a poorer prognosis

ANSWER

 

606-3. Which of the following confers a significantly increased risk of this disorder?

  1. HTLV-I
  2. Down syndrome
  3. HIV
  4. Myelodysplastic syndrome
  5. Infectious mononucleosis

ANSWER

 

 

CASE NUMBER 605, UMich slide 42610nl
[ImageScope] [WebScope] -courtesy of UMich

Clinical History: A 45-year old woman presents with marked splenomegaly. Her leukocyte count is increased to 300,000/uL. The differential count reveals the presence of small numbers of myeloblasts and promyelocytes, with a predominance of myelocytes, metamyelocytes, bands, and segemented neutrophils. Basophils are also increased in number, as are platelets. The patient is not anemic. Leukocyte alkaline phosphatase is decreased. The peripheral blood film is shown.

Image Gallery:

(Summary of Microscopic Findings)

The red cells show two populations – some are hypochromic while others are microspherocytic (small and without central pallor). The latter are likely transfused red cells. The white cells are almost all blasts. They vary from 1.5x to 3x the diameter of red cells, have large round to slightly indented nuclei which occupy almost the entire cell (very high nuclear to cytoplasmic ratio). They have fine or reticular nuclear chromatin, 1-3 nucleoli, and a small amount of cytoplasm, which is without granules in most blasts. Platelets are not seen.

(Review Blood Histology)
Norm No. 29 Lymph node

Normal blood smear 63x (Wright stain)
[ImageScope] [WebScope]

Normal blood smear 86x (Wright stain)
[ImageScope] [WebScope]

Scan around the 63x and 86x slides at high magnification to see the various kinds of blood cells that were discussed in the lecture.  Most abundant, of course, are the red blood cells (RBCs) or erythrocytes, which are seen in large numbers everywhere you look.  In between the RBCs you should look for small, basophilic fragments which are platelets or thrombocytes [example] that are important in blood clotting.  As you continue viewing, you will see occasional white blood cells (leukocytes).  Some of the white blood cells may defy identification, often because the cells were damaged during slide preparation, so look for characteristic examples, and ignore the equivocal cells. Refer to the images in your texts and from the lecture and try to find an example of each leukocyte type using the 63x and 86x slides (there's less area to cover in these high-mag slides and the cells present are excellent, although the 63x slide does NOT contain any basophils).

The most common white blood cell is the neutrophil, which has a distinct multi-lobed nucleus (often 3-5 lobes).  Also frequently seen are lymphocytes, which are small cells (often as small as RBCs) with a dark nucleus and very little cytoplasm.  Another cell type is the monocyte, the largest of the blood cells.  It has a large, relatively pale nucleus, and rather clear cytoplasm (granules are usually less apparent than those in the illustration in W).  You will also see an occasional eosinophil, with prominent reddish granules filling the cytoplasm, and a nucleus with 2 (or sometimes 3) lobes.  The exact color of the granules may vary from slide to slide, depending on how well the slide was prepared.  In your particular slides they may be anywhere from bright red to dull brown.  The remaining cell type you may see on your slides is the basophil, which is hard to find, since it constitutes less than 1% of the leukocytes (the 86x slide actually has THREE excellent examples).  The cytoplasm contains large, irregular granules in a "grape-cluster" appearance that usually stain dark blue or almost black. Basophil nuclei may often appear somewhat oval-shaped, so, at first glance, they may be confused with lymphocytes. However, the presence of the large, dark-staining granules should help you distinguish them; also, remember that basophils are rare.

After you've done some looking on your own, here some quick links showing examples of each type of leukocyte (in order of their normal frequency in a blood smear):

605-1. What is the differential diagnosis?

ANSWER

 

605-2. Which of the following describes a major characteristic of this disorder?

  1. Chromosome 9;22 translocation
  2. Expansion of mature B Lymphocytes within multiple lymph nodes
  3. Hypogammaglobulinemia
  4. Neoplastic cells exhibiting hair-like filamentous projections
  5. Peak incidence at 65 years of age

ANSWER

 

Part 2, UMich slide 55182nl
[ImageScope] [WebScope] -courtesy of UMich

She undergoes therapy with imatinib mesylate (tyrosine kinase inhibitor), which reduces the spleen size and brings the total leukocyte count within normal range.  She remains in remission for 3 years and then begins to experience fatigue and a 10-kg weight loss.  Physical examination now shows petechial hemorrhages.  CBC shows hemoglobin of 10.5 g/dL, hematocrit 30%, platelet count 60,000 µL, and WBC count 40,000/µL. A peripheral blood film is shown in the virtual slide (UMich_55182nl) and illustrated in the image below. Karyotypic analysis shows two Ph chromosomes and aneuploidy.  Flow cytometric analysis of the peripheral blood shows CD19+, CD10+, sIg-, CD3- cells.

Image Gallery:

605-3. Which of the following complications of the initial disease did this patient develop following therapy?

  1. Sézary syndrome
  2. Myelodysplastic syndrome
  3. Hairy cell leukemia
  4. B-lymphoblastic leukemia
  5. Acute myeloid leukemia

ANSWER

 

 

 

HEMATOPATHOLOGY Review Items

Key Genetic Transformations Associated with Leukemias

  • Follicular Lymphoma: t (14; 18) resulting in BCL2-IgH fusion gene
  • Mantle cell Lymphoma: t (11; 14) resulting in CyclinD1-IgH fusion gene
  • Adult T cell leukemia/lymphoma: HTLV-1 provirus
  • AML with Auer rods:  t (15:17)(q22:11-12) resulting in RARA/PML fusion gene
  • CML: t (9;22) “Philadelphia chromosome” resulting in BCR-ABL fusion
  • Burkitt Lymphoma: translocations involving MYC and Ig loci, usually t (8:14). Subset associated with EBV.

 

Key Vocabulary Terms (click here to search any additional terms on Stedman's Online Medical Dictionary)

achlorhydria leukemia
acute leukemia  leukemoid reaction
agnogenic (idiopathic) myeloid metaplasia leukocytosis
aleukemic leukemia leukoerythroblastosis
amyloidosis leukopenia
anemia lymphoma
anisocytosis  macrocytosis
autosplenectomy marginating pool
basophilic stippling maturation/storage pool
Bence Jones protein mean cell hemoglobin (MCH)
Birbeck granule (HX body) mean cell hemoglobin concentration (MCHC)
bronchus-associated lymphoid tissue (BALT) mean cell volume (MCV)
chronic leukemia microcytosis
circulating pool mucosa-associated lymphoid tissue (MALT)
coagulation myelodysplastic syndrome
complete blood count (CBC) myelophthisic syndrome
cryoglobulinemia myeloproliferative disorder
direct antiglobulin (Coombs) test nuclear-cytoplasmic asynchrony
dyserythropoiesis pancytopenia
dysmegakaryocytopoiesis petechiae
ecchymoses Philadelphia chromosome
erythropoiesis Plummer-Vinson syndrome
erythropoietin poikilocytosis
extramedullary hematopoiesis polychromasia
extravascular hemolysis proliferating pool
ferritin purpura
G6PD screen red cell distribution width (RDW)
granulocytopenia reticulocyte count
granulopoiesis Schilling test
haptoglobin sickle cell disease
hematocrit sickle cell prep
hematoma sickle cell trait
hemoglobin electrophoresis stem cell
hemostasis thalassemia 
hyperviscosity syndrome thrombocytopenia
hypochromia thrombocytosis
idiopathic thrombocytopenic purpura (ITP) thrombopoiesis
indirect antiglobulin (Coombs) test thrombopoietin
ineffective hematopoiesis thrombotic thromocytopenic purpura (TTP)
intravascular hemolysis total iron binding capacity (TIBC)
intrinsic factor transferrin

LEARNING OBJECTIVES

Absolutely critical information you must know to practice medicine is in bold font.
Important information that will be needed for routine patient care is in regular font.
Information about less common diseases that you may encounter in clinical practice and that will probably appear on examinations is in italics

  1. Define and state the significance of each of these peripheral blood smear findings:

  2. Define and state the significance of each of the following cells on a bone marrow smear:

  3. Explain:
    • the concept of reference (normal) range
    • the theory of the automated cell counter
    • the components of the complete blood count (CBC)
    • CBC application in patient evaluation

  4. Compare and contrast the reporting of leukocyte differential counts as relative percentages vs. absolute numbers, in terms of the advantages and disadvantages of each system.

  5. Discuss the stages of erythropoiesis in terms of:
    • morphology of each stage
    • stages in which hemoglobin is produced
    • lifespan of reticulocytes and mature red blood cells
    • mechanisms of degradation of senescent erythrocytes
    • factors (vitamin, minerals and hormones) which influence erythropoiesis

  6. Discuss the stages of granulopoiesis in terms of:
    • morphology of each stage
    • time to form and life span of mature granulocytes
    • basic functions of the different types of maturing granulocytes
    • factors which influence granulopoiesis.

  7. Discuss the stages of development of lymphocytes, plasma cells, and monocytes, in terms of:
    • morphology
    • life span of mature forms
    • functions of mature forms
    • factors which influence production.

  8. Discuss thrombocytopoiesis in terms of:
    • morphology of megakaryocytes
    • fate of megakaryocytes
    • life span of platelets
    • factors which influence thrombocytopoiesis
    • abnormal morphologic forms of platelets and megakaryocytes

  9. Discuss the following classification of anemia in terms of rationale for its use, and specific examples in each category:
  10. Categorize and discuss laboratory test procedures used in the diagnosis of anemia, outlining the basic workup of a patient who presents with anemia.

  11. Assess bone marrow function in the diagnosis of the anemic patient, on the basis of:
    • reticulocyte count (relative, absolute, and corrected)
    • serum bilirubin
    • urobilinogen concentration

  12. Discuss the clinical and pathologic features of the following types of anemia:
  13. Utilize peripheral blood and bone marrow smears to assess the deviations from normal marrow response which occur in:
    • hemolytic anemias
    • nuclear maturation defects
    • cytoplasmic maturation defects
    • hypoproliferative anemias

  14. Compare and contrast anemia secondary to acute vs. chronic blood loss
    • etiology
    • pathophysiologic changes
    • clinicopathologic diagnosis

  15. Discuss the clinical and pathologic features of these types of anemia:
  16. Compare and contrast warm vs. cold antibody immunohemolytic anemias in terms of:
    • etiology
    • pathogenesis
    • associated risks-diseases
    • laboratory diagnosis
    • clinical features and course

  17. Compare and contrast intravascular vs. extravascular hemolysis, in terms of:
    • etiology
    • pathogenesis
    • laboratory diagnosis
    • clinical findings and course

  18. Compare and contrast clinical and pathologic features of :
  19. Describe the WHO classification of acute myeloblastic leukemias in  terms of:
    • nomenclature
    • incidence of each type
    • general features of each type

  20. List the major etiology and pathogenesis of the following:

  21. Distinguish between leukemia and leukemoid reaction on the basis of:
    • etiology
    • pathogenesis
    • laboratory data

  22. Morphologically differentiate a blast from a monocyte and lymphocyte.

  23. Discuss the clinical and pathologic features of these myelodysplastic syndromes:
  24. Define and classify the myeloproliferative disorders.

  25. Discuss the clinical and pathologic features of these myeloproliferative disorders:
  26. Compare and contrast the clinical and pathologic features of:
  27. Describe the proper mode of submission of a lymph node biopsy to the surgical pathology laboratory for workup of a suspected lymphoproliferative disorder.

  28. Define, state the significance of, and identify in a microscopic section of a lymph node or extranodal site of involvement each of the following:
  29. Compare and contrast the clinical and pathologic features of follicular hyperplasia and follicular lymphoma.

  30. Discuss general features of non-Hodgkin lymphoma in terms of:
    • incidence
    • immunophenotyping (T vs B cells)
    • morphologic patterns (diffuse vs. follicular)
    • principles of:
    • classification (WHO)
    • grading
    • staging
    • laboratory methods of diagnosis
    • clinical features
    • prognosis
    • extra lymphatic organs involved
    • likelihood of a leukemic phase

  31. Compare and contrast the clinical and pathologic features of :
  32. Compare and contrast clinical and pathologic features of:
  33. Discuss Hodgkin lymphoma in terms of:
    • classification
    • morphology of each type
    • incidence of each type
    • laboratory diagnosis
    • etiology
    • clinical features
    • pathogenesis
    • prognosis

  34. Compare and contrast the clinical and pathologic features of :
  35. Discuss clinical and pathologic features of:
  36. List benign and malignant etiologies of lymphadenopathy and splenomegaly.

  37. Categorize and discuss the different types of plasma cell dyscrasias in terms of definitions and clinical presentation.

  38. Discuss clinical and pathologic features of multiple myeloma.

  39. Discuss clinical and pathologic features of Waldenström macroglobulinemia.

  40. Compare and contrast the clinical and pathologic features of:
  41. Discuss the different laboratory procedures used in the clinicopathologic diagnosis of the different plasma cell dyscrasias.

  42. List benign and malignant etiologies of monoclonal gammopathies.

  43. Discuss the clinical and pathologic features of Langerhans cell histiocytosis.

  44. Classify major causes of changes in size of the spleen, either increasing OR decreasing.

  45. Discuss Hodgkin lymphoma in terms of:
    • infarcts
    • amyloid
    • sickle cell disease
    • leukemia
    • extramedullary hematopoiesis
    • lymphoma
    • passive congestion
    • rupture

  46. List the major complications of splenomegaly.

  47. Briefly describe the morphologic features and clinical findings in:
  48. Discuss thrombocytopenia in terms of:
    • differential diagnosis
    • clinical features
    • bone marrow morphology and
    • laboratory features

  49. Discuss thrombocytosis in terms of diagnosis and differential diagnosis.

  50. Outline the role of platelets in normal hemostasis.

  51. Outline the process for stepwise evaluation of a patient with suspected platelet disorder.

  52. Compare and contrast the following disorders of platelets the clinical and pathologic:
     

  53. Categorize and discuss acquired disorders of platelet function.

  54. Compare and contrast clinical and pathologic features of:
  55. List and discuss the laboratory diagnostic procedures used to approach patients with:
    • bleeding disorders
    • thrombotic disorders

  56. Discuss the pathophysiology of disseminated intravascular coagulopathy (DIC).

 

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