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Characteristics of malignant lymphoma typically include

overproliferation of neutrophils

overproliferation of lymphocytes

lymph node involvement

more than one possible answer

none of these choices

CLL symptoms frequently include


weight loss, anemia, and extreme leukocytosis

absolute lymphocytosis, edema, and splenic infarction

absolute lymphocytosis, malaise, and low-grade fever

neutrophilia, splenomegaly, and anemia

more than one possible answer

two possible answers

All of the following mature lymphoid neoplasms are considered indolent disease, except. Select all that
apply.

Hairy cell leukemia

Burkitt leukemia

Multiple myeloma

Mycosis fungoides

Sezary syndrome

Follicular lymphoma
Chronic lymphocytic leukemia

Prolymphocytic leukemia

Which of the following immunophenotypic markers are observed in CLL/SLL patients. Select all that
apply.
CD19 (2)

CD20 (2)

CD11c

CD5 (2)

CD10 eh negative yung 10 ?????

CD2

CD4

Which of the following is not considered a disorder of plasma cells?


monoclonal gammopathy of undetermined
significance

multiple myeloma

Sezary syndrome (1) QUIZLET

Waldenstrom macroglobulinemia

more than one possible answer

none of these choices


Which of the following cells is considered pathognomonic for Hodgkin's disease?
Flame cells

Reactive lymphocytes

Mott / Morula cells

Reed-Sternberg cells
https://quizlet.com/405631484/
medical-laboratory-science-revi
ew-harr-17-hematology-lympho
proliferatrive-and-myeloprolifer
artive-disorders-flash-cards/

more than one possible answer

two possible choices

Multiple myeloma exhibits the following laboratory features. Select all that apply.
occasional plasma cells in the peripheral blood (tama na ba to?)

*Not sure with occasional plasma cells in the peripheral blood – sabi
sa book “Overt involvement of peripheral blood by circulating plasma cells is
relatively rare until advanced or end-stage disease develop.”

Rouleaux

Hypercalcemia

decreased immunoglobulin

What is the most probable mature lymphoid neoplasm given this peripheral blood smear:
https://drive.google.com/file/d/12fTaFb14rW9OSwTv33UC0GR8qwUSeSto/vincoew?usp=sharing
Burkitt lymphoma/leukemia

Sezary syndrome

Chronic Lymphocytic Leukemia

Hairy cell leukemia

Classic Hodgkin Lymphoma

Lymphocyte-Predominant Hodgkin Lymphoma

None of these choices


A 78-year-old man was previously diagnosed with CLL. Periodic CBCs were ordered, and several months
of CBCs maintained an appearance consistent with cases of CLL. Current result shows WBC 110 x
10^12/L, Differential: 70% lymphocytes, 8% segmented neutrophils, 2% monocytes, 20% unidentified
cells with lymphoid appearance and a prominent nucleolus. Which of the following is most likely.
The patient developed Sezary syndrome

The patient has developed prolymphocytic leukemia

The patient has developed multiple myeloma

The patient now has a concurrent case of CLL and


ALL

more than one possible answer

none of these choices

A dry tap may be seen in bone marrow aspirations in all of the following conditions, except:
aplastic anemia

hairy cell leukemia

multiple myeloma

primary myelofibrosis

none of these conditions, all may cause dry tap

Which of the following immunophenotypic markers are observed in Burkitt lymphoma patients. Select all
that apply.
CD19

CD20

CD11c

CD5

CD10

CD2

CD4

1 points
What is the most probable mature lymphoid neoplasm given this peripheral blood smear:
https://drive.google.com/file/d/1C_pynxJI0MXPTP8DWaca2uVzz8JEpDgs/view?usp=sharing

Burkitt lymphoma/leukemia

Sezary syndrome

Chronic Lymphocytic Leukemia

Hairy cell leukemia

Classic Hodgkin Lymphoma

Lymphocyte-Predominant Hodgkin Lymphoma


None of these choices????? (1) HOT-DOG
HOY WITHOUT THE DASH NGA will u go
with none na?? Baka mag none me same
same oki i passed na heheh nag none me k

Which of the following appearances describes the type of cell seen in Sezary syndrome?
plasma cells containing immunoglobulin deposits

large circulating micromegakaryocytes

lymphocytes with convoluted, cerebriform, nuclei (1)

prolymphocytes with prominent azurophilic granules

none of these choices

WM is characterized by increased levels of


IgG

IgM

IgD

IgA

none of these choices

Reed-Sternberg cell is a large binucleated cell with a dense nucleolus surrounded by clear space. RS cell
is described with characteristic "owl's eye" appearance
Only the first statement is correct

Only the second statement is correct

Both statements are correct

Both statements are incorrect

What is the most probable mature lymphoid neoplasm given this peripheral blood smear:
https://drive.google.com/file/d/1oyfXPkUoXwR09EXeO5wsdI4IR9AfAy21/view?usp=sharing
Burkitt lymphoma/leukemia

Sezary syndrome

Chronic Lymphocytic Leukemia

Hairy cell leukemia


Classic Hodgkin Lymphoma

Lymphocyte-Predominant Hodgkin Lymphoma

None of these choices - Should be Adult T


Cell Lymphoma/Leukemia

Which of the following immunophenotypic markers are observed in Hairy Cell Leukemia patients. Select
all that apply.
CD19

CD20

CD11c

CD5

CD10 (negative ata siya sa 10?


Check table) negative siya!!

CD2

CD4

Indolent B cell lymphoma commonly due to chronic antigen stimulation either in the setting of infection or
autoimmunity
Mantle cell lymphoma

Mycosis fungoides

Marginal Zone lymphoma

Follicular lymphoma

none of these choices

Multiple myeloma is a disorder of


T lymphocytes

Megakaryocytes

Plasma cells

Lymph nodes

more than one possible answer

none of these choices


If a 65-year-old female with swollen lymph nodes has a CBC performed and many smudge cells were
noted along with lymphocytosis, a probably diagnosis might be
chronic lymphocytic leukemia

multiple myeloma

Hodgkin disease

mantle cell lymphoma

none of these choices

All of the following are associated with the diagnosis of multiple myeloma. Select all that apply.
marrow plasmacytosis

Lytic bone lesions

monoclonal gammopathy
di toh kasali under siya ng
philadelphia

Philadelphia chromosome

In Hodgkin lymphoma the Reed-Sternberg cell and _________ are malignant.


Popcorn cells

T cells

B cells

Histiocytes

Waldenstrom's macroglobulinemia is a malignancy of the:


Lymphoplasmacytoid cells

Adrenal cortex

myeloblastic cell lines

erythroid cell precursors

none of these choices

Multiple myeloma and Waldenstrom's macroglobulinemia have all the following in common. Select all that
apply.
monoclonal gammopathy

hyperviscosity of the blood

Rouleaux formation

Osteolytic lesions

The most common lymphoma in young adults is


follicular lymphoma

mycosis fungoides

Hodgkin lymphoma

diffuse large B-cell lymphoma

none of these choices

The pathology of multiple myeloma includes which of the following? Select all that apply.
expanding plasma cell mass

overproduction of monoclonal immunoglobulins

production of osteoclast activating factor (OAF) to increase bone resorption and release of
calcium

normal bone marrow is gradually replaced by the malignant plasma cells

release of free light chains in the urine

The diagnostic type seen in Hodgkin lymphoma is:


binucleate plasma cell

Reed Sternberg cell


Sezary cell

Burkitt cell

What is the most probable mature lymphoid neoplasm given this peripheral blood smear:
https://drive.google.com/file/d/12fTaFb14rW9OSwTv33UC0GR8qwUSeSto/view?usp=sharing
Burkitt lymphoma/leukemia

Sezary syndrome

Chronic Lymphocytic Leukemia

Hairy cell leukemia

Classic Hodgkin Lymphoma

Lymphocyte-Predominant Hodgkin Lymphoma

None of these choices

What is the most probable mature lymphoid neoplasm given this peripheral blood smear:
https://drive.google.com/file/d/1cyw2uqlCGPyIAcIiJty3QJ-RTZvKdfXG/view?usp=sharing

Burkitt lymphoma/leukemia

Sezary syndrome

Chronic Lymphocytic Leukemia

Hairy cell leukemia

Classic Hodgkin Lymphoma

Lymphocyte-Predominant Hodgkin Lymphoma

None of these choices


CLL is classically a
T-cell disorder

B-cell disorder

null cell disorder

plasma cell

Cells that exhibit a positive stain with acid phosphatase and are not inhibited with tartaric acid are
characteristically seen in:
Burkitt's lymphoma

Infection lymphocytosis

Hairy cell leukemia

T-cell acute lymphoblastic leukemia

Multiple myeloma

more than one possible answer

none of these choices

MGUS is characterized by
monoclonal immunoglobulin in a patient's serum in the presence of solitary mass of plasma
cells (4)

significant infiltration of the bone marrow with plasma cells but only a few clinical symptoms of
multiple myeloma

monoclonal immunoglobulin in a patient's serum with only a small percentage of infiltration of


bone marrow with plasma cells

significant infiltration of the bone marrow with plasma cells and monoclonal immunoglobulin in
both the patient's serum and urine
Which of the following mature lymphoid neoplasms are considered aggressive disease. Select all that
apply. Kung ano green yun lang yun
Hairy cell leukemia

Burkitt leukemia

Multiple myeloma

Mycosis fungoides

Sezary syndrome
Follicular lymphoma

Chronic lymphocytic leukemia

Prolymphocytic leukemia

Which cluster designation are positive in typical HCL?


CD25, CD11c, CD19, CD4

CD25, CD11c, CD19, CD10

CD25, CD11c, CD10, CD5

CD25, CD11c, CD19, CD20

none of these choices


dapat 25, 22, 19 ,20
The diagnostic type seen in Hodgkin lymphoma is:
binucleate plasma cell

Reed Sternberg cell

Sezary cell

Burkitt cell

The abnormal protein frequently found in the urine of persons with multiple myeloma is
albumin

globulin

IgG

Bence Jones proteins

none of these choices

Multiple myeloma can be difficult to distinguish from:


chronic lymphocytic leukemia

acute myelogenous leukemia

monoclonal gammopathy of undetermined significance

benign adenoma

more than one possible answer


none of these choices

Most common form of Non-Hodgkin lymphoma


Mantle cell lymphoma

Mycosis fungoides

Marginal Zone lymphoma

Follicular lymphoma
(hindi ba none?? Under
lang to ng DLBCL eh??)

none of these choices


none same

Which of the following is a finding seen in the peripheral smear of a patient with multiple myeloma?
microcytic hypochromic cells

intracellular inclusion bodies

rouleaux

hypersegmented neutrophils

more than one possible answer

none of these choices

A 75-year-old male patient visits his physician for an annual checkup. His CBC showed an elevated EBC
count with numerous small lymphocytes and smudge cells, and a subsequent bone marrow biopsy and
aspirate showed hypercellularity with increased lymphoid cells. What is a presumptive diagnosis based on
this information?
Hairy cell leukemia

Chronic lymphocytic leukemia

Multiple Myeloma

Hodgkin lymphoma

Mycosis fungoides

more than one possible answer

none of these choices

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