Course Content
Blood & Immunology Module — 3rd Year MBBS
AIM • KMU Exam Reasoning

KMU Past Paper Practice

Lymphoid Neoplasms, Lymphomas and Plasma Cell Disorders

3rd Year MBBS • 20 A-Type Single Best Answer MCQs

MCQ 1

Question:

A 10-year-old child with acute lymphoblastic leukemia undergoes molecular testing after B-cell lineage has been established. A fusion protein with constitutive tyrosine kinase activity is identified. Which genetic abnormality best explains this finding?

Options:

t(14;18) involving BCL2
BCR-ABL1 fusion
t(11;14) involving cyclin D1
MYC-immunoglobulin rearrangement
Deletion involving chromosome 17p
Correct Answer: BCR-ABL1 fusion
Explanation: BCR-ABL1 is an important molecular abnormality in a subgroup of B-ALL and produces abnormal tyrosine kinase signaling that promotes leukemic-cell survival and proliferation.

MCQ 2

Question:

A child is diagnosed with B-lineage acute lymphoblastic leukemia. Cytogenetic analysis shows an increased number of chromosomes within the leukemic clone rather than a specific translocation. Which abnormality best describes this finding?

Options:

Monosomy
Tetraploidy
Deletion 13q
Hyperdiploidy
Trisomy 12
Correct Answer: Hyperdiploidy
Explanation: Hyperdiploidy refers to an increased chromosome number and represents an important genetic pattern in a subgroup of B-ALL.

MCQ 3

Question:

An adolescent with acute lymphoblastic leukemia develops headache and neurological symptoms. The bone marrow already contains a confirmed lymphoblast population. Which pathological process best accounts for the new presentation?

Options:

Infiltration of the central nervous system by lymphoblasts
Deposition of monoclonal immunoglobulin in neural tissue
Transformation of lymphoblasts into plasma cells
Formation of reactive germinal centers in the meninges
Accumulation of mature neutrophils around cranial nerves
Correct Answer: Infiltration of the central nervous system by lymphoblasts
Explanation: ALL may extend beyond marrow and blood to the central nervous system; neurological manifestations can therefore result from leukemic infiltration.

MCQ 4

Question:

A 69-year-old woman presents with painless generalized lymphadenopathy. Lymph-node biopsy shows a mature small B-cell neoplasm, while significant peripheral blood lymphocytosis is absent. Which diagnosis best represents this tissue-predominant manifestation?

Options:

B-lymphoblastic lymphoma
Marginal zone lymphoma
Mantle cell lymphoma
Follicular lymphoma
Small lymphocytic lymphoma
Correct Answer: Small lymphocytic lymphoma
Explanation: CLL and SLL are closely related manifestations of the same mature B-cell neoplasm; predominant lymph-node involvement favors the designation SLL.

MCQ 5

Question:

Flow cytometry in an elderly patient demonstrates a clonal mature B-cell population suspected to represent CLL. Compared with many other mature B-cell neoplasms, which additional immunophenotypic feature supports this interpretation?

Options:

Strong surface immunoglobulin with absent CD19
Strong CD20 expression with absent CD23
Weak CD20 and weak surface immunoglobulin expression
Strong TdT expression with absent mature B-cell markers
Strong CD30 expression with absent surface immunoglobulin
Correct Answer: Weak CD20 and weak surface immunoglobulin expression
Explanation: CLL cells characteristically show relatively weak CD20 and surface immunoglobulin expression compared with many other mature B-cell lymphomas.

MCQ 6

Question:

A patient with a plasma-cell neoplasm has a monoclonal immunoglobulin composed predominantly of free light chains without a major intact heavy-chain component. Which type of multiple myeloma best fits this pattern?

Options:

IgG myeloma
Light-chain myeloma
IgA myeloma
Nonsecretory myeloma
Solitary plasmacytoma
Correct Answer: Light-chain myeloma
Explanation: Light-chain myeloma is characterized predominantly by production of monoclonal free immunoglobulin light chains rather than intact immunoglobulin molecules.

MCQ 7

Question:

A 61-year-old patient has a localized mass composed of clonal plasma cells at a single site. Evaluation does not show the widespread marrow involvement characteristic of disseminated myeloma. Which plasma-cell neoplasm is most appropriate?

Options:

IgA myeloma
Light-chain myeloma
Nonsecretory myeloma
CLL with plasmacytic change
Plasmacytoma
Correct Answer: Plasmacytoma
Explanation: A plasmacytoma is a localized clonal plasma-cell tumor, whereas multiple myeloma characteristically involves multiple marrow sites.

MCQ 8

Question:

Bone-marrow examination in a plasma-cell neoplasm shows cells with deeply basophilic cytoplasm. Which cellular feature most directly accounts for this staining pattern?

Options:

Abundant rough endoplasmic reticulum
Numerous cytoplasmic lysosomes
Accumulated glycogen granules
Excess intracellular calcium
Numerous lipid vacuoles
Correct Answer: Abundant rough endoplasmic reticulum
Explanation: Plasma cells synthesize large amounts of immunoglobulin, requiring abundant rough endoplasmic reticulum and producing strongly basophilic cytoplasm.

MCQ 9

Question:

A patient with multiple myeloma shows evidence of disease progression. Molecular testing demonstrates a newly acquired abnormality affecting a pathway known to promote cellular growth. Which change is recognized as a secondary abnormality during progression?

Options:

ETV6-RUNX1 activation
HTLV-1 integration
BCL2 translocation alone
RAS pathway abnormality
T-cell receptor rearrangement
Correct Answer: RAS pathway abnormality
Explanation: Additional abnormalities involving pathways such as RAS may accumulate during myeloma progression and support further growth of the malignant plasma-cell clone.

MCQ 10

Question:

A patient with suspected plasma-cell myeloma has a distinct monoclonal protein in serum. Which investigation is most useful for further characterizing the immunoglobulin type produced by the clone?

Options:

Peripheral blood differential count
Bone mineral radiography alone
Immunofixation
Lymph-node immunohistochemistry
Reticulocyte estimation
Correct Answer: Immunofixation
Explanation: Immunofixation characterizes a detected monoclonal immunoglobulin and helps identify the heavy- and light-chain type produced by the plasma-cell clone.

MCQ 11

Question:

A 55-year-old man has generalized lymphadenopathy. Biopsy shows numerous classical Reed-Sternberg cells surrounded by lymphocytes, eosinophils, plasma cells and histiocytes without broad collagen bands. Which subtype is most likely?

Options:

Lymphocyte-rich classical Hodgkin lymphoma
Nodular sclerosis classical Hodgkin lymphoma
Nodular lymphocyte-predominant Hodgkin lymphoma
Lymphocyte-depleted classical Hodgkin lymphoma
Mixed cellularity classical Hodgkin lymphoma
Correct Answer: Mixed cellularity classical Hodgkin lymphoma
Explanation: Mixed cellularity Hodgkin lymphoma contains classical Reed-Sternberg cells within a prominent mixed inflammatory background of several reactive cell types.

MCQ 12

Question:

Histological examination of a lymph node shows classical Hodgkin lymphoma with relatively few normal lymphocytes and a prominent population of highly atypical tumor cells. Which subtype best matches this pattern?

Options:

Mixed cellularity classical Hodgkin lymphoma
Lymphocyte-depleted classical Hodgkin lymphoma
Lymphocyte-rich classical Hodgkin lymphoma
Nodular sclerosis classical Hodgkin lymphoma
Nodular lymphocyte-predominant Hodgkin lymphoma
Correct Answer: Lymphocyte-depleted classical Hodgkin lymphoma
Explanation: Lymphocyte-depleted classical Hodgkin lymphoma shows relatively sparse normal lymphocytes with more conspicuous atypical malignant cells.

MCQ 13

Question:

A lymph-node specimen is diagnosed as classical Hodgkin lymphoma. Viral studies demonstrate Epstein-Barr virus within the malignant B-cell-derived population. Which interpretation is most appropriate?

Options:

EBV can provide survival signals in a proportion of cases
EBV indicates a mature T-cell origin of the tumor
EBV converts the tumor into a plasma-cell neoplasm
EBV proves that the lesion is Burkitt lymphoma
EBV produces the collagen bands of nodular sclerosis
Correct Answer: EBV can provide survival signals in a proportion of cases
Explanation: EBV is associated with a subset of classical Hodgkin lymphomas and can contribute survival signaling, but it is not present in every case.

MCQ 14

Question:

A patient develops a malignant T-cell proliferation after infection with a human retrovirus. Which lymphoma is most strongly associated with this infectious agent?

Options:

Extranodal NK/T-cell lymphoma
Primary effusion lymphoma
Gastric MALT lymphoma
Adult T-cell leukemia/lymphoma
Follicular lymphoma
Correct Answer: Adult T-cell leukemia/lymphoma
Explanation: HTLV-1 is the characteristic infectious association of adult T-cell leukemia/lymphoma and promotes abnormal T-cell proliferation and survival.

MCQ 15

Question:

A lymphoma involving the nasal region is classified as an extranodal NK/T-cell neoplasm. Which infectious agent has the strongest association with this entity?

Options:

Helicobacter pylori
HTLV-1
Epstein-Barr virus
HHV-8
Hepatitis B virus
Correct Answer: Epstein-Barr virus
Explanation: Extranodal NK/T-cell lymphoma has a strong association with EBV, making viral association an important pathological clue to this entity.

MCQ 16

Question:

An immunocompromised patient develops a lymphoma presenting predominantly as a malignant body-cavity effusion without a typical solid nodal mass. Which viral association best fits this lymphoma?

Options:

HHV-8
HTLV-1
Helicobacter pylori
Hepatitis C virus
Parvovirus B19
Correct Answer: HHV-8
Explanation: Primary effusion lymphoma is characteristically associated with HHV-8 and may present as malignant fluid accumulation in body cavities.

MCQ 17

Question:

A pathologist examines an enlarged lymph node containing a relatively uniform population of atypical lymphoid cells replacing much of the normal tissue. Which feature most strongly favors lymphoma over a reactive lymph-node response?

Options:

Preserved sinus architecture
Mixed population of reactive cells
Prominent normal germinal centers
Intact medullary structures
Monomorphic abnormal lymphoid population
Correct Answer: Monomorphic abnormal lymphoid population
Explanation: Many lymphomas produce a relatively monomorphic neoplastic population, whereas reactive nodes typically contain a heterogeneous mixture of lymphoid and inflammatory cells.

MCQ 18

Question:

A patient has persistent painless lymphadenopathy and lymphoma is suspected. The clinician wants the pathologist to assess both the abnormal lymphoid cells and their arrangement within the node. Which specimen approach best serves this purpose when feasible?

Options:

Peripheral blood smear only
Excisional lymph-node biopsy
Serum immunoglobulin measurement
Bone radiography alone
Urine protein examination only
Correct Answer: Excisional lymph-node biopsy
Explanation: Excisional biopsy preserves lymph-node architecture, allowing evaluation of both cellular morphology and the nodular, diffuse or other growth pattern needed for lymphoma classification.

MCQ 19

Question:

A lymph-node biopsy shows an abnormal follicular pattern. The pathologist applies antibodies directly to tissue sections to determine whether the cells express markers supporting mature B-cell differentiation. Which investigation is being used?

Options:

Serum electrophoresis
Cytogenetic karyotyping
Bone-marrow aspiration
Immunohistochemistry
Urinary light-chain analysis
Correct Answer: Immunohistochemistry
Explanation: Immunohistochemistry detects lineage and differentiation markers directly within tissue while preserving the relationship between marker expression and lymph-node architecture.

MCQ 20

Question:

A lymphoid malignancy is being classified according to its normal cellular counterpart. The tumor expresses mature T-cell markers and lacks features of an immature precursor neoplasm. Which category of lymphoid neoplasm is most appropriate?

Options:

Precursor B-cell neoplasm
Plasma-cell neoplasm
Mature T-cell/NK-cell neoplasm
Precursor T-cell neoplasm
Classical Hodgkin lymphoma
Correct Answer: Mature T-cell/NK-cell neoplasm
Explanation: WHO-style classification groups lymphoid tumors by lineage and maturation stage; mature T-lineage tumors therefore belong to the mature T-cell/NK-cell category.

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