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PA H8 | Lymphadenopathy & Lymphomas — Practice Quiz

Practice 14 questions · Untimed · Unlimited attempts

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Q1 PA19.1 1 pt

A 22-year-old student presents with a 3-week history of bilateral posterior cervical lymphadenopathy. The nodes are soft, tender, and measure 1.5 cm. He has fever, sore throat, and fatigue. Peripheral blood smear shows atypical lymphocytes. Which of the following is the most appropriate initial diagnostic step?

A Excision biopsy of the largest node
B Fine needle aspiration cytology (FNAC) of a node
C Monospot test and Epstein-Barr virus serology
D CT scan of neck and chest

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Q2 PA19.1 1 pt

A 45-year-old woman is referred with a 2 cm, firm, non-tender left axillary lymph node of 6 weeks duration. She has no fever or weight loss. Ultrasound shows a round node with loss of fatty hilum. What is the most appropriate next investigation?

A Watchful waiting for 4 more weeks
B Core needle / excision biopsy
C FNAC
D PET-CT scan

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Q3 PA19.2 1 pt

Histology of a reactive lymph node shows enlarged follicles with prominent germinal centres containing tingible-body macrophages, a well-defined mantle zone, and a mixed population of centroblasts and centrocytes. The interfollicular areas appear normal. Which type of reactive hyperplasia pattern is this?

A Paracortical hyperplasia
B Follicular (nodular) hyperplasia
C Sinus histiocytosis
D Mixed pattern hyperplasia

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Q4 PA19.3 1 pt

A 30-year-old male presents with cervical lymphadenopathy, low-grade fever, and night sweats for 8 weeks. FNAC reveals epithelioid granulomas with central caseous necrosis and occasional Langhans-type giant cells. Ziehl-Neelsen stain shows acid-fast bacilli. Which of the following best describes the gross appearance of the involved node at surgery?

A Firm white nodule with fish-flesh cut surface
B Cheesy yellow-white material that crumbles on sectioning
C Haemorrhagic soft node with necrotic foci
D Gelatinous clear material filling the sinuses

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Q5 PA19.3 1 pt

A histopathology report describes a lymph node with non-caseating epithelioid granulomas, no central necrosis, no acid-fast bacilli on ZN stain, and negative cultures. Serum ACE is elevated. The most likely diagnosis is:

A Tuberculosis lymphadenitis
B Sarcoidosis
C Cat-scratch disease
D Fungal lymphadenitis

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Q6 PA19.5 1 pt

On histology of a Hodgkin lymphoma lymph node biopsy, large binucleated cells with prominent 'owl-eye' nucleoli are seen in a background of lymphocytes, eosinophils, plasma cells, and neutrophils. Immunohistochemistry shows CD15+ and CD30+ on these cells. CD20 and CD3 are negative. What is the cell type identified?

A Lacunar cell
B Reed-Sternberg cell
C Centroblast
D Immunoblast

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Q7 PA19.5 1 pt

A 28-year-old woman is diagnosed with classical Hodgkin lymphoma, nodular sclerosis subtype. Staging reveals involvement of the right cervical and mediastinal lymph nodes. If disease progresses untreated, to which site would lymphoma most characteristically spread next, according to its pattern of dissemination?

A Liver via haematogenous spread
B Left cervical nodes and then para-aortic nodes via contiguous nodal spread
C Bone marrow via early haematogenous dissemination
D Skin via retrograde lymphatic spread

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Q8 PA19.5 1 pt

Biopsy of a large mediastinal mass in a 20-year-old woman shows bands of collagen dividing the nodal tissue into cellular nodules. Lacunar cells are identified within these nodules, alongside lymphocytes and eosinophils. CD30 and CD15 immunostains are positive on the large cells. What is the subtype of Hodgkin lymphoma?

A Mixed cellularity Hodgkin lymphoma
B Nodular sclerosis Hodgkin lymphoma
C Lymphocyte-rich Hodgkin lymphoma
D Lymphocyte-depleted Hodgkin lymphoma

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Q9 PA19.5 1 pt

EBV is most strongly associated with which subtype of classical Hodgkin lymphoma?

A Nodular sclerosis
B Lymphocyte-rich
C Mixed cellularity
D Lymphocyte-depleted

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Q10 PA19.6 1 pt

A 55-year-old man presents with painless generalised lymphadenopathy and hepatosplenomegaly for 6 months. Lymph node biopsy shows effacement of nodal architecture by follicle-like structures composed predominantly of small cleaved lymphocytes (centrocytes) with occasional large cells. Immunohistochemistry: CD20+, BCL2+, CD10+, BCL6+, CD5−. Cytogenetics shows t(14;18). What is the diagnosis?

A Mantle cell lymphoma
B Follicular lymphoma
C Chronic lymphocytic leukaemia/small lymphocytic lymphoma
D Marginal zone lymphoma

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Q11 PA19.6 1 pt

A 65-year-old woman presents with a rapidly enlarging abdominal mass of 6 weeks duration, constitutional B-symptoms, and elevated LDH. Biopsy shows large cells with vesicular nuclei, prominent nucleoli, and abundant cytoplasm effacing the nodal architecture in a diffuse pattern. IHC: CD20+, BCL6+, MUM1+. What is the most likely diagnosis?

A Follicular lymphoma, grade 3
B Diffuse large B-cell lymphoma (DLBCL)
C Burkitt lymphoma
D T-cell/histiocyte-rich large B-cell lymphoma

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Q12 PA19.6 1 pt

A 10-year-old boy in sub-Saharan Africa presents with a rapidly enlarging jaw mass. Biopsy shows intermediate-sized lymphoid cells with round nuclei, multiple small nucleoli, and a high mitotic rate. A 'starry-sky' pattern is noted due to scattered macrophages engulfing apoptotic debris. Ki-67 approaches 100%. EBER in situ hybridisation is positive. Which chromosomal translocation is most characteristic of this tumour?

A t(14;18)(q32;q21) — BCL2 rearrangement
B t(8;14)(q24;q32) — MYC-IGH rearrangement
C t(11;14)(q13;q32) — cyclin D1 rearrangement
D t(2;5)(p23;q35) — ALK rearrangement

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Q13 PA19.5 1 pt

A 42-year-old man presents with fever, drenching night sweats, unexplained weight loss >10% body weight, and non-tender left cervical lymphadenopathy. A 32-year-old woman in the same clinic has bilateral painless inguinal lymphadenopathy, no constitutional symptoms, and a slow-growing mass over 18 months. Which clinical distinction most helps differentiate Hodgkin from Non-Hodgkin lymphoma in these presentations?

A HL typically presents in older adults; NHL is a disease of young adults
B HL tends to present with contiguous nodal spread and mediastinal involvement in young adults; NHL more often presents with non-contiguous, peripheral, or extranodal disease
C HL never causes B-symptoms; NHL always does
D NHL is always CD20-negative; HL is always CD20-positive

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Q14 PA19.6 1 pt

A 17-year-old boy presents with fever, right-sided jaw swelling, and abdominal distension over 3 weeks. CT scan shows a jaw mass and retroperitoneal lymphadenopathy. LDH is 5 times the upper limit of normal. Biopsy of the jaw mass reveals intermediate-sized monomorphic lymphoid cells with scanty cytoplasm, round nuclei with multiple nucleoli, and a starry-sky pattern. Ki-67 is 99%. FISH confirms t(8;14). Serum uric acid is markedly elevated. Which statement best describes the pathogenesis of the starry-sky pattern in this tumour?

A Reactive T-lymphocytes infiltrating between tumour cells
B Benign macrophages engulfing apoptotic tumour cell debris against a dark background of densely packed neoplastic cells
C Scattered Reed-Sternberg cells in a pale inflammatory background
D Follicular dendritic cells forming a meshwork within neoplastic follicles

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